Publications of the Biosynthesis / NMR Research Group

Department	Year	Citation like

in press

Heiling, S., Cortés Llorca, L., Li, J., Gase, K., Schmidt, A., Schaefer, M., Schneider, B., Halitschke, R., Gaquerel, E., Baldwin, I. T. (in press). Specific decorations of 17-hydroxygeranyllinalool diterpene glycosides solve the autotoxicity problem of chemical defense in Nicotiana attenuata. bioRxiv. doi:10.1101/2020.08.26.267690. [ITB627]

2021

Li, J., Halitschke, R., Li, D., Paetz, C., Su, H., Heiling, S., Xu, S., Baldwin, I. T. (2021). Controlled hydroxylations of diterpenoids allow for plant chemical defense without autotoxicity. Science, 371(6526), 255-260. doi:10.1126/science.abe4713. [ITB633]

Schmiech, M., Ulrich, J., Lang, S. J., Büchele, B., Paetz, C., St-Gelais, A., Syrovets, T., Simmet, T. (2021). 11-keto-alpha-boswellic acid, a novel triterpenoid from Boswellia spp. with chemotaxonomic potential and antitumor activity against triple-negative breast cancer cells. Molecules, 26(2): 366. doi:10.3390/molecules26020366. [NMR272]

Stavenga, D. G., Leertouwer, H. L., Dudek, B., van der Kooi, C. J. (2021). Coloration of flowers by flavonoids and consequences of pH dependent absorption. Frontiers in Plant Science, 11: 600124. doi:10.3389/fpls.2020.600124. [IMPRS107]

2020

Dong, C., Dolke, F., Bandi, S., Paetz, C., von Reuss, S. H. (2020). Dimerization of conserved ascaroside building blocks generates species-specific male attractants in Caenorhabditis nematodes. Organic & Biomolecular Chemistry, 18(27), 5253-5263. doi:10.1039/D0OB00799D. [BOL710]

Dudek, B., Schneider, B., Hilger, H. H., Stavenga, D. G., Martínez-Harms, J. (2020). Highly different flavonol content explains geographic variations in the UV reflecting properties of flowers of the corn poppy, Papaver rhoeas (Papaveraceae). Phytochemistry, 178: 112457. doi:10.1016/j.phytochem.2020.112457. [NMR270]

Israni, B., Wouters, F. C., Luck, K., Seibel, E., Ahn, S.-J., Paetz, C., Reinert, M., Vogel, H., Erb, M., Heckel, D. G., Gershenzon, J., Giddings Vassão, D. (2020). The fall armyworm Spodoptera frugiperda utilizes specific UDP-glycosyltransferases to inactivate maize defensive benzoxazinoids. Frontiers in Physiology, 11: 604754. doi:10.3389/fphys.2020.604754. [GER619]

Lackus, N., Müller, A., Kröber, T., Reichelt, M., Schmidt, A., Nakamura, Y., Paetz, C., Luck, K., Lindroth, R. L., Constabel, C. P., Unsicker, S., Gershenzon, J., Köllner, T. G. (2020). The occurrence of sulfated salicinoids in poplar and their formation by sulfotransferase 1. Plant Physiology, 183(1), 137-151. doi:10.1104/pp.19.01447. [GER593]

Lang, S. J., Schmiech, M., Hafner, S., Paetz, C., Werner, K., Gaafary, M. E., Schmidt, C. Q., Syrovets, T., Simmet, T. (2020). Chrysosplenol d, a flavonol from Artemisia annua, induces ERK1/2-mediated apoptosis in triple negative human breast cancer cells. International Journal of Molecular Sciences, 21(11): 4090. doi:10.3390/ijms21114090. [NMR268]

Malka, O., Easson, M. E. A. M., Paetz, C., Götz, M., Reichelt, M., Stein, B., Luck, K., Stanišic, A., Juravel, K., Santos-Garcia, D., Mondaca, L. L., Springate, S., Colvin, J., Winter, S., Gershenzon, J., Morin, S., Giddings Vassão, D. (2020). Glucosylation prevents plant defense activation in phloem-feeding insects. Nature Chemical Biology, 16, 1429-1426. doi:10.1038/s41589-020-00658-6. [GER612]

Nemesio-Gorriz, M., Menezes, R. C., Paetz, C., Hammerbacher, A., Steenackers, M., Schamp, K., Höfte, M., Svatoš, A., Gershenzon, J., Douglas, G. C. (2020). Canditate metabolites for ash dieback tolerance in Fraxinus excelsior. The Journal of Experimental Biology, 71(19), 6074-6083. doi:10.1093/jxb/eraa306. [MS207]

Rodriguez, H. A., Hidalgo, W. F., Sanchez, J. D., Menezes, R. C., Schneider, B., Arango, R. E., Morales, J. G. (2020). Differential regulation of jasmonic acid pathways in resistant (Calcutta 4) and susceptible (Williams) banana genotypes during the interaction with Pseudocercospora fijiensis. Plant Pathology, 69(5), 872-882. doi:10.1111/ppa.13165. [NMR267]

Rodríguez-López, C. E., Hong, B., Paetz, C., Nakamura, Y., Koudounas, K., Passeri, V., Baldoni, L., Alagna, F., Calderini, O., O’Connor, S. E. (2020). Two bi-functional cytochrome P450 CYP72 enzymes from olive (Olea europaea) catalyze the oxidative C-C bond cleavage in the biosynthesis of secoxy-iridoids – flavor and quality determinants in olive oil. New Phytologist. doi:10.1111/nph.16975. [SOC106]

Scognamiglio, M., Schneider, B. (2020). Identification of potential allelochemicals from donor plants and their synergistic effects on the metabolome of Aegilops geniculata. Frontiers in Plant Science, 11: 1046. doi:10.3389/fpls.2020.01046. [NMR269]

Zare, S., Mirkhani, H., Firuzi, O., Moheimanian, N., Asadollahi, M., Pirhadi, S., Chandran, J. N., Schneider, B., Jassbi, A. R. (2020). Antidiabetic and cytotoxic polyhydroxylated oleanane and ursane type triterpenoids from Salvia grossheimii. Bioorganic Chemistry, 104: 104297. doi:10.1016/j.bioorg.2020.104297. [NMR271]

2019

Chen, Y., Paetz, C., Schneider, B. (2019). Organ-specific distribution and non-enzymatic conversions indicate a metabolic network of phenylphenalenones in Xiphidium caeruleum. Phytochemistry, 159, 30-38. doi:10.1016/j.phytochem.2018.12.004. [NMR258]

Désiré, S., Ernestine, N., Bruno, T. B., Lazare, S. S., Ulrich, D. D., Lateef, M., Schneider, B., Ali, M. S., Barthélemy, N. (2019). A new dammarane type triterpene glucoside from the aerial parts of Gouania longipetala (Rhamnaceae). Natural Product Research. doi:10.1080/14786419.2019.1690483. [NMR265]

Dolke, F., Dong, C., Bandi, S., Paetz, C., Glauser, G., von Reuß, S. H. (2019). Ascaroside signaling in the bacterivorous nematode Caenorhabditis remanei encodes the growth phase of its bacterial food source. Organic Letters, 21(15), 5832-5837. doi:10.1021/acs.orglett.9b01914. [BOL716]

Fu, N., Yang, Z.-l., Pauchet, Y., Paetz, C., Brandt, W., Boland, W., Burse, A. (2019). A cytochrome P450 from juvenile mustard leaf beetles hydroxylates geraniol, a key step in iridoid biosynthesis. Insect Biochemistry and Molecular Biology, 113: 103212. doi:10.1016/j.ibmb.2019.103212. preprint available [BOL713]

Günther, A., Schöning, I., Martin, M. J., Paetz, C. (2019). Verbreitung, Ökologie und Inhaltsstoffe von Boletopsis grisea (Peck) Bondartsev & Singer: Ein rezentes Vorkommen in Jena. Zeitschrift für Mykologie, 85(1), 31-51. [NMR259]

Hölscher, D. (2019). Cellular-specific detection of polyphenolic compounds by NMR-and MS-based techniques. In H. Halbwirth, K. Stich, V. Cheynier, S. Quideau (Eds.), Recent Advances in Polyphenol Research (pp. 149-181). John Wiley & Sons Ltd. [NMR263]

Lackner, S., Lackus, N., Paetz, C., Köllner, T. G., Unsicker, S. (2019). Aboveground phytochemical responses to belowground herbivory in poplar trees and the consequence for leaf herbivore preference. Plant, Cell and Environment, 42(12), 3293-3307. doi:10.1111/pce.13628. [GER578]

Lang, S. J., Schmiech, M., Hafner, S., Paetz, C., Steinborn, C., Huber, R., Gaafary, M. E., Werner, K., Schmidt, C. Q., Syrovets, T., Simmet, T. (2019). Antitumor activity of an Artemisia annua herbal preparation and identification of active ingredients. Phytomedicine, 62: 152962. doi:10.1016/j.phymed.2019.152962. [NMR266]

Lyu, H., Liu, W., Bai, B., Shan, Y., Paetz, C., Feng, X., Chen, Y. (2019). Prenyleudesmanes and a hexanorlanostane from the roots of Lonicera macranthoides. Molecules, 24(23): 4276. doi:10.3390/molecules24234276. [NMR264]

Mirzaei, H. H., Firuzi, O., Chandran, J. N., Schneider, B., Jassbi, A. R. (2019). Two antiproliferative seco-4,5-abietane diterpenoids from roots of Salvia ceratophylla L. Phytochemistry Letters, 29, 129-133. doi:10.1016/j.phytol.2018.11.017. [NMR257]

Schubert, T., von Reuß, S. H., Kunze, C., Paetz, C., Kruse, S., Brand-Schön, P., Nelly, A. M., Nüske, J., Diekert, G. (2019). Guided cobamide biosynthesis for heterologous production of reductive dehalogenases. Microbial Biotechnology, 12(2), 346-359. doi:10.1111/1751-7915.13339. [NMR260]

Sree, K. S., Dahse, H.-M., Chandran, J. N., Schneider, B., Jahreis, G., Appenroth, K. J. (2019). Duckweed for human nutrition: No cytotoxic and no anti-proliferative effects on human cell lines. Plant Foods for Human Nutrition, 74(2), 223-224. doi:10.1007/s11130-019-00725-x. [NMR261]

2018

Beran, F., Sporer, T., Paetz, C., Ahn, S.-J., Betzin, F., Kunert, G., Shekhov, A., G. Vassão, D., Bartram, S., Lorenz, S., Reichelt, M. (2018). One pathway is not enough: The cabbage stem flea beetle Psylliodes chrysocephala uses multiple strategies to overcome the glucosinolate-myrosinase defense in its host plants. Frontiers in Plant Science, 9: 1754. doi:10.3389/fpls.2018.01754. [BER004]

Berg, A., Oner, E. T., Combie, J., Schneider, B., Ellinger, R., Weisser, J., Wyrwa, R., Schnabelrauch, M. (2018). Formation of new, cytocompatible hydrogels based on photochemically crosslinkable levan methacrylates. International Journal of Biological Macromolecules, 107(Part B), 2312-2319. doi:10.1016/j.ijbiomac.2017.10.120. [NMR246]

Carqueijeiro, I., de Bernonville, T. D., Lanoue, A., Dang, T.-T., Teijaro, C., Paetz, C., Billet, K., Mosquera, A., Oudin, A., Besseau, S., Papon, N., Glévarec, G., Atehortùa, L., Clastre, M., Giglioli-Guivarc'h, N., Schneider, B., St-Pierre, B., Andrade, R. B., O’Connor, S. E., Courdavault, V. (2018). A BAHD acyltransferase catalyzing 19-O-acetylation of tabersonine derivatives in roots of Catharanthus roseus enables combinatorial synthesis of monoterpene indole alkaloids. The Plant Journal, 49(3), 469-484. doi:10.1111/tpj.13868. [NMR249]

Chen, Y., Paetz, C., Schneider, B. (2018). Precursor-directed biosynthesis of phenylbenzoisoquinolindione alkaloids and the discovery of a phenylphenalenone-based plant defense mechanism. Journal of Natural Products, 81(4), 879-884. doi:10.1021/acs.jnatprod.7b00885. [NMR251]

Dudek, B., Schnurrer, F., Dahse, H.-M., Paetz, C., Warskulat, A.-C., Weigel, C., Voigt, K., Schneider, B. (2018). Formation of nudicaulins in vivo and in vitro and the biomimetic synthesis and bioactivity of O-methylated nudicaulin derivatives. Molecules, 23(12): 3357. doi:10.3390/molecules23123357. [NMR256]

Feistel, F., Paetz, C., Menezes, R. C., Veit, D., Schneider, B. (2018). Acylated quinic acids are the main salicortin metabolites in the lepidopteran specialist herbivore Cerura vinula. Journal of Chemical Ecology, 44(5), 497-509. doi:10.1007/s10886-018-0945-1. [NMR253]

Keller, A., Kunze, D., Bommer, L., Paetz, C., Menezes, R. C., Svatoš, A., Dobbek, H., Schubert, T. (2018). Selective utilization of benzimidazolyl-norcobamides as cofactors by the tetrachloroethene reductive dehalogenase of Sulfurospirillum multivorans. Journal of Bacteriology, 200(8): e00584-17. doi:10.1128/JB.00584-17. [NMR254]

Krieger, C., Roselli, S., Galati, G., Kellner-Thielmann, S., Schneider, B., Grosjean, J., Orly, A., Ritchie, D., Matern, U., Bourgaud, F., Hehn, A. (2018). The CYP71AZ P450 subfamily: a driving factor for the diversification of coumarin biosynthesis in apiaceous plants. Frontiers in Plant Science, 9: 820. doi:10.3389/fpls.2018.00820. [NMR255]

Martínez-Harms, J., Warskulat, A.-C., Dudek, B., Kunert, G., Lorenz, S., Hansson, B. S., Schneider, B. (2018). Biosynthetic and functional color-scent associations in flowers of Papaver nudicaule and its impact on pollinators. Chembiochem, 19(14), 1553-1562. doi:10.1002/cbic.201800155. [HAN307]

Michal Johnson, J., Thürich, J., Petutschnig, E. K., Altschmied, L., Meichsner, D., Sherameti, I., Dindas, J., Mrozinska, A., Paetz, C., Scholz, S. S., Furch, A. C. U., Lipka, V., Hedrich, R., Schneider, B., Svatoš, A., Oelmüller, R. (2018). A poly(A) ribonuclease controls the cellotriose-based interaction between Piriformospora indica and its host Arabidopsis. Plant Physiology, 176(1), 2496-2514. doi:10.1104/pp.17.01423. [NMR248]

Nakamura, Y., Paetz, C., Boland, W. (2018). Synthesis of methyl 4-dihydrotrisporate B and methyl trisporate B, morphogenetic factors of Zygomycetes fungi. Zeitschrift für Naturforschung, C: Journal of Biosciences, 73(1), 59-66. doi:10.1515/znc-2017-0148. [BOL686]

Naseri, M., Emami, S. A., Asili, J., Tayarani-Najaran, Z., Dehghan, G., Schneider, B., Iranshahi, M. (2018). Rupestrines A-D, alkaloids from the aerial parts of Corydalis rupestris. Bioorganic Chemistry, 77, 651-659. doi:10.1016/j.bioorg.2018.02.019. [NMR250]

Soltani, S., Amin, G.-R., Salehi-Sourmaghi, M. H., Schneider, B., Lorenz, S., Iranshahi, M. (2018). Sulfur-containing compounds from the roots of Ferula latisecta and their cytotoxic activities. Fitoterapia, 124, 108-112. doi:10.1016/j.fitote.2017.10.012. [NMR247]

Stavrinides, A. K., Tatsis, E. C., Dang, T.-T., Caputi, L., Stevenson, C. E. M., Lawson, D. M., Schneider, B., O'Connor, S. E. (2018). Discovery of a short-chain dehydrogenase from Catharanthus roseus that produces a novel monoterpene indole alkaloid. Chembiochem, 19(9), 940-948. doi:10.1002/cbic.201700621. [NMR252]

Wang, M., Schäfer, M., Li, D., Halitschke, R., Dong, C.-F., McGale, E., Paetz, C., Song, Y., Li, S., Dong, J., Heiling, S., Groten, K., Franken, P., Bitterlich, M., Harrison, M., Paszkowski, U., Baldwin, I. T. (2018). Blumenols as shoot markers for root symbiosis with arbuscular mycorrhizal fungi. eLife, 7: e37093. doi:10.7554/eLife.37093. [ITB589]

Wirth, S., Kunert, M., Ahrens, L., Krause, K., Broska, S., Paetz, C., Kniemeyer, O., Jung, E., Boland, W., Kothe, E. (2018). The regulator of G-protein signaling Thn1 links pheromone response to volatile production in Schizophyllum commune. Environmental Microbiology, 20(10), 3684-3699. doi:10.1111/1462-2920.14369. [BOL703]

2017

Berasategui, A., Salem, H., Paetz, C., Santoro, M., Gershenzon, J., Kaltenpoth, M., Schmidt, A. (2017). Gut microbiota of the pine weevil degrades conifer diterpenes and increases insect fitness. Molecular Ecology, 26(15), 4099-4110. doi:10.1111/mec.14186. [GER478]

Brkljaca, R., Schneider, B., Hidalgo, W., Otálvaro, F., Ospina, F., Lee, S., Hoshino, M., Fujita, M., Urban, S. (2017). Application of the crystalline sponge method to revise the structure of the phenalenone fuliginone. Molecules, 22(2): 211. doi:10.3390/molecules22020211. [NMR239]

Chen, Y., Paetz, C., Menezes, R. C., Schneider, B. (2017). Cultured roots of Xiphidium caeruleum: Phenylphenalenones and their biosynthetic and extractant-dependent conversion. Phytochemistry, 133, 15-25. doi:10.1016/j.phytochem.2016.10.011. [NMR237]

Crecelius, A. C., Hölscher, D., Hoffmann, T., Schneider, B., Fischer, T. C., Hanke, M.-V., Flachowsky, H., Schwab, W., Schubert, U. S. (2017). Spatial and temporal localization of flavonoid metabolites in strawberry fruit (Fragaria × ananassa). Journal of Agricultural and Food Chemistry, 65(17), 3559-3568. doi:10.1021/acs.jafc.7b00584. [NMR241]

Feistel, F., Paetz, C., Lorenz, S., Beran, F., Kunert, G., Schneider, B. (2017). Idesia polycarpa (Salicaceae) leaf constituents and their toxic effect on Cerura vinula and Lymantria dispar (Lepidoptera) larvae. Phytochemistry, 143, 170-179. doi:10.1016/j.phytochem.2017.08.008. [NMR245]

Hölscher, D., Vollrath, A., Kai, M., Dhakshinamoorthy, S., Menezes, R. C., Svatoš, A., Schubert, U. S., Buerkert, A., Schneider, B. (2017). Local phytochemical response of Musa acuminata x balbisiana Colla cv. ‘Bluggoe’ (ABB) to colonization by Sternorrhyncha. Phytochemistry, 133, 26-32. doi:10.1016/j.phytochem.2016.10.007. [NMR238]

Jassbi, A. R., Eghtesadi, F., Hazeri, N., Ma’sumi, H., Valizadeh, J., Chandran, J. N., Schneider, B., Baldwin, I. T. (2017). The roots of Salvia rhytidea: a rich source of biologically active diterpenoids. Natural Product Research, 31(4), 477-481. doi:10.1080/14786419.2016.1188096. [ITB525]

Jassbi, A. R., Vafapour, M., Shokrollahi, A., Firuzi, O., Zare, M., Chandran, J. N., Schneider, B., Baldwin, I. T. (2017). Cytotoxic activity of two cembranoid diterpenes from Nicotiana sylvestris against three human cancer cell lines. The Open Bioactive Compounds Journal, 05, 1-8. doi:10.2174/1874847301705010001. [ITB567]

Mageroy, M. H., Jancsik, S., Yuen, M. M. S., Fischer, M., Withers, S. G., Paetz, C., Schneider, B., MacKay, J. J., Bohlmann, J. (2017). A conifer UDP-sugar dependent glycosyltransferase contributes to acetophenone metabolism and defense against insects. Plant Physiology, 175(2), 641-651. doi:10.1104/pp.17.00611. [NMR242]

Mirzaei, H. H., Firuzi, O., Schneider, B., Baldwin, I. T., Jassbi, A. R. (2017). Cytotoxic diterpenoids from the roots of Salvia lachnocalyx. Revista Brasileira de Farmacognosia, 27(4), 475-479. doi:10.1016/j.bjp.2017.01.009. [ITB544]

Ocampos, F. M. M., Paetz, C., Antar, G. M., Menezes, R. C., Miguel, O. G., Schneider, B. (2017). Phytochemical profile of Schiekia orinocensis (Haemodoraceae). Phytochemistry Letters, 21, 139-145. doi:10.1016/j.phytol.2017.06.008. [NMR244]

Ospina, F., Ramirez, A., Cano, M., Hidalgo, W., Schneider, B., Otálvaro, F. (2017). Synthesis of positional isomeric phenylphenalenones. The Journal of Organic Chemistry, 82(7), 3873-3879. doi:10.1021/acs.joc.6b02985. [NMR240]

Schneider, B. (2017). Phenylphenalenone glycosides: Occurrence, structure revision, and substituent effects on the steric orientation. Phytochemistry Letters, 21, 104-108. doi:10.1016/j.phytol.2017.06.004. [NMR243]

Wang, M., Schoettner, M., Xu, S., Paetz, C., Wilde, J., Baldwin, I. T., Groten, K. (2017). Catechol, a major component of smoke, influences primary root growth and root hair elongation through reactive oxygen species-mediated redox signaling. New Phytologist, 213(4), 1755-1770. doi:10.1111/nph.14317. [ITB534]

2016

Boeckler, A., Paetz, C., Feibicke, P., Gershenzon, J., Unsicker, S. (2016). Metabolism of poplar salicinoids by the generalist herbivore Lymantria dispar (Lepidoptera). Insect Biochemistry and Molecular Biology, 78, 39-49. doi:10.1016/j.ibmb.2016.08.001. [GER456]

Chen, Y., Paetz, C., Menezes, R. C., Schneider, B. (2016). Phenylbenzoisoquinolindione alkaloids accumulate in stamens of Xiphidium caeruleum Aubl. flowers. Phytochemistry, 128, 95-101. doi:10.1016/j.phytochem.2016.05.002. [NMR230]

Dudek, B., Warskulat, A.-C., Schneider, B. (2016). The occurrence of flavonoids and related compounds in flower sections of Papaver nudicaule. Plants, 5: 28. doi:10.3390/plants5020028. [NMR229]

Fang, J., Ramsay, A., Renouard, S., Hano, C., Lamblin, F., Chabbert, B., Mesnard, F., Schneider, B. (2016). Laser microdissection and spatiotemporal pinoresinol-lariciresinol reductase gene expression assign the cell layer-specific accumulation of secoisolaricirésinol diglucoside in flaxseed coats. Frontiers in Plant Science, 7: 1743. doi:10.3389/fpls.2016.01743. [NMR236]

Handrick, V., Robert, C. A. M., Ahern, K. R., Zhou, S., Machado, R. A. R., Maag, D., Glauser, G., Fernandez-Penny, F. E., Chandran, J. N., Rodgers-Melnike, E., Schneider, B., Buckler, E. S., Boland, W., Gershenzon, J., Jander, G., Erb, M., Köllner, T. G. (2016). Biosynthesis of 8-O-methylated benzoxazinoid defense compounds in maize. The Plant Cell, 28(7), 1682-1700. doi:10.1105/tpc.16.00065. [GER442]

Hidalgo, W., Cano, M., Arbelaez, M., Zarrazola, E., Gil, J., Schneider, B., Otálvaro, F. (2016). 4-Phenylphenalenones as a template for new photodynamic compounds against Mycosphaerella fijiensis. Pest Management Science, 72(4), 796-800. doi:10.1002/ps.4055. [NMR222]

Hidalgo, W., Chandran, J. N., Menezes, R. C., Otálvaro, F., Schneider, B. (2016). Phenylphenalenones protect banana plants from infection by Mycosphaerella fijiensis and are deactivated by metabolic conversion. Plant, Cell and Environment, 39(3), 492-513. doi:10.1111/pce.12630. [NMR223]

Hölscher, D., Buerkert, A., Schneider, B. (2016). Phenylphenalenones accumulate in plant tissues of two banana cultivars in response to herbivory by the banana weevil and banana stem weevil. Plants, 5(3): 34. doi:10.3390/plants5030034. [NMR233]

Iranshahy, M., Tayarani-Najaran, Z., Kasaian, J., Ghandadi, M., Emami, S. A., Asili, J., Chandran, J. N., Schneider, B., Iranshahi, M. (2016). Highly oxygenated sesquiterpene lactones from Cousinia aitchisonii and their cytotoxic properties: Rhaserolide induces apoptosis in human T lymphocyte (Jurkat) cells via the activation of c-Jun N-terminal kinase phosphorylation. Phytotherapy Research, 30(2), 222-226. doi:10.1002/ptr.5519. [NMR226]

Jassbi, A. R., Firuzi, O., Miri, R., Salhei, S., Zare, S., Zare, M., Masroorbabanari, M., Chandran, J. N., Schneider, B., Baldwin, I. T. (2016). Cytotoxic activity and chemical constituents of Anthemis mirheydari. Pharmaceutical Biology, 54(10), 2044-2049. doi:10.3109/13880209.2016.1141220. [ITB515]

Jassbi, A. R., Mirzaei, Y., Firuzi, O., Chandran, J. N., Schneider, B. (2016). Bioassay guided purification of cytotoxic natural products from a red alga Dichotomaria obtusata. Revista Brasileira de Farmacognosia, 26(6), 705-709. doi:10.1016/j.bjp.2016.06.008. [NMR232]

Liu, Y., Luo, S.-H., Schmidt, A., Wang, G.-D., Sun, G.-L., Grant, M., Kuang, C., Yang, M.-J., Jing, S.-X., Li, C.-H., Schneider, B., Gershenzon, J., Li, S.-H. (2016). A geranylfarnesyl diphosphate synthase provides the precursor for sesterterpenoid (C25) formation in the glandular trichomes of the mint Leucosceptrum canum. The Plant Cell, 28(3), 804-822. doi:10.1105/tpc.15.00715. [GER436]

Ospina, F., Hidalgo, W., Cano, M., Schneider, B., Otálvaro, F. (2016). Synthesis of 8-Phenylphenalenones: 2-Hydroxy-8-(4-hydroxyphenyl)-1H-phenalen-1-one from Eichhornia crassipes. The Journal of Organic Chemistry, 81(3), 1256-1262. doi:10.1021/acs.joc.5b02559. [NMR228]

Paetz, C., Hammerbacher, A., Menezes, R. C., Feistel, F., Weigel, C., Voigt, K., Schneider, B. (2016). Chemical composition and antimicrobial activity of Populus nigra shoot resin. Natural Product Communications, 11(7), 989-992. doi:10.1177/1934578X1601100730. [NMR231]

Pauls, G., Becker, T., Rahfeld, P., Gretscher, R., Paetz, C., Pasteels, J., von Reuss, S. H., Burse, A., Boland, W. (2016). Two defensive lines in juvenile leaf beetles; esters of 3-nitropropionic acid in the hemolymph and aposematic warning. Journal of Chemical Ecology, 42(3), 240-248. doi:10.1007/s10886-016-0684-0. [BOL645]

Ramsay, A., Fliniaux, O., Quéro, A., Molinie, R., Dly, H., Hano, C., Paetz, C., Roscher, A., Grand, E., Kovensky, J., Schneider, B., Mesnard, F. (2016). Kinetics of the incorporation of the main phenolic compounds into the lignan macromolecule during flaxseed development. Food Chemistry, 217, 1-8. doi:10.1016/j.foodchem.2016.08.039. [NMR234]

Ritter, M., Seidel, R. A., Bellstedt, P., Schneider, B., Bauer, M., Görls, H., Pohnert, G. (2016). Isolation and identification of intermediates of the oxidative bilirubin degradation. Organic Letters, 18(17), 4432-4435. doi:10.1021/acs.orglett.6b02287. [FGP001]

Stanton, M., Preßler, J., Paetz, C., Boland, W., Svatoš, A., Baldwin, I. T. (2016). Plant-mediated pheromone emission by a hemipteran seed feeder increases the apparency of an unreliable but rewarding host. New Phytologist, 211(1), 113-125. doi:10.1111/nph.13879. [ITB516]

Wadke, N., Kandasamy, D., Vogel, H., Lah, L., Wingfield, B. D., Paetz, C., Wright, L., Gershenzon, J., Hammerbacher, A. (2016). The bark-beetle-associated fungus, Endoconidiophora polonica, utilizes the phenolic defense compounds of its host as a carbon source. Plant Physiology, 171(2), 914-931. doi:10.1104/pp.15.01916. [GER448]

Warskulat, A.-C., Tatsis, E., Dudek, B., Kai, M., Lorenz, S., Schneider, B. (2016). An unprecedented utilization of pelargonidin and indole for the biosynthesis of plant indole alkaloids. Chembiochem, 17(4), 318-327. doi:10.1002/cbic.201500572. [NMR227]

2015

Baranovskii, A. V., Bolibrukh, D. A., Schneider, B. (2015). Synthesis of 14alpha-substituted Androstanes—key compounds in the synthesis of 14-substituted Brassinosteroids. Russian Journal of Organic Chemistry, 51(1), 78-85. doi:10.1134/S1070428015010133. [NMR216]

Baranovsky, A., Bolibrukh, D. A., Schneider, B. (2015). Solvolysis of 14,17-etheno-bridged 16alpha-nitroestratrienyl acetate and lactam formation pathways studied by LC-NMR and LC-MS. Structures of minor products. Steroids, 104, 37-48. doi:10.1016/j.steroids.2015.08.009. [NMR224]

Becker, T., Kartikeya, P., Paetz, C., von Reuß, S. H., Boland, W. (2015). Synthesis and photosensitivity of isoxazolin-5-one glycosides. Organic & Biomolecular Chemistry, 13, 4025-4030. doi:10.1039/C5OB00244C. [BOL618]

Boachon, B., Junker, R. R., Miesch, L., Bassard, J.-E., Höfer, R., Caillieaudeaux, R., Seidel, D. E., Lesot, A., Heinrich, C., Ginglinger, J.-F., Allouche, L., Vincent, B., Wahyuni, D. S., Paetz, C., Beran, F., Miesch, M., Schneider, B., Leiss, K., Werck-Reichhart, D. (2015). CYP76C1 (Cytochrome P450)-mediated linalool metabolism and the formation of volatile and soluble Linalool oxides in Arabidopsis flowers: A strategy for defense against floral antagonists. The Plant Cell, 27(10), 2972-2990. doi:10.1105/tpc.15.00399. [NMR225]

Chitsazian-Yazdi, M., Agnolet, S., Lorenz, S., Schneider, B., Es’haghi, Z., Kasaian, J., Khameneh, B., Iranshahi, M. (2015). Foetithiophenes C-F, thiophene derivatives from the roots of Ferula foetida. Pharmaceutical Biology, 53(5), 710-714. doi:10.3109/13880209.2014.939765. [NMR211]

Fatangare, A., Paetz, C., Saluz, H., Svatoš, A. (2015). 2-Deoxy-2-fluoro-D-glucose metabolism in Arabidopsis thaliana. Frontiers in Plant Science, 6: 935. doi:10.3389/fpls.2015.00935. [MS174]

Feistel, F., Paetz, C., Lorenz, S., Schneider, B. (2015). The absolute configuration of salicortin, HCH-salicortin and tremulacin from Populus trichocarpa × deltoides Beaupré. Molecules, 20, 5566-5573. doi:10.3390/molecules20045566. [NMR217]

Gaafary, M. E., Büchele, B., Syrovets, T., Agnolet, S., Schneider, B., Schmidt, C. Q., Simmet, T. (2015). An alpha-acetoxy-tirucallic acid isomer inhibits Akt/mTOR signaling and induces oxidative stress in prostate cancer cells. Journal of Pharmacology and Experimental Therapeutics, 352(1), 33-42. doi:10.1124/jpet.114.217323. [NMR213]

González-Cabanelas, D., Wright, L., Paetz, C., Onkokesung, N., Gershenzon, J., Concepción, M. R., Phillips, M. A. (2015). The diversion of 2-C-methyl-D-erythritol-2,4-cyclodiphosphate from the 2-C-methyl-D-erythritol 4-phosphate pathway to hemiterpene glycosides mediates stress responses in Arabidopsis thaliana. The Plant Journal, 82(1), 122-137. doi:10.1111/tpj.12798. [GER405]

Hidalgo, W., Kai, M., Schneider, B. (2015). 4-Methoxycinnamic acid – An unusual phenylpropanoid involved in phenylphenalenone biosynthesis in Anigozanthos preissii. Phytochemistry, 117, 476-481. doi:10.1016/j.phytochem.2015.05.017. [NMR221]

Hölscher, D., Fuchser, J., Knop, K., Menezes, R. C., Buerkert, A., Svatoš, A., Schubert, U. S., Schneider, B. (2015). High resolution mass spectrometry imaging reveals the occurrence of phenylphenalenone-type compounds in red paracytic stomata and red epidermis tissue of Musa acuminata ssp. zebrina cv. ‘Rowe Red’. Phytochemistry, 116, 239-245. doi:10.1016/j.phytochem.2015.04.010. [NMR218]

Huber, M., Triebwasser-Freese, D., Reichelt, M., Heiling, S., Paetz, C., Chandran, J. N., Bartram, S., Schneider, B., Gershenzon, J., Erb, M. (2015). Identification, quantification, spatiotemporal distribution and genetic variation of major latex secondary metabolites in the common dandelion (Taraxacum officinale agg.). Phytochemistry, 115, 89-98. doi:10.1016/j.phytochem.2015.01.003. [GER406]

Kamarozaman, A. S., Latip, J., Paetz, C., Syah, Y. M. (2015). Monomer stilbenoid glucosides from Vatica pauciflora and Vatica lowii (Dipterocarpaceae). Jurnal Teknologi, 77(2), 69-72. doi:10.11113/jt.v77.5989. [NMR262]

Lu, X., Dittgen, J., Pislewska-Bednarek, M., Molina, A., Schneider, B., Svatoš, A., Doubský, J., Schneeberger, K., Weigel, D., Bednarek, P., Schulze-Lefert, P. (2015). Mutant allele-specific uncoupling of PENETRATION3 functions reveals engagement of the ATP-binding cassette transporter in distinct tryptophan metabolic pathways. Plant Physiology, 168, 814-827. doi:10.1104/pp.15.00182. [MS170]

Martin, N. J., Ferreiro, S. F., Barbault, F., Nicolas, M., Lecellier, G., Paetz, C., Gaysinski, M., Alonso, E., Thomas, O. P., Botana, L. M., Raharivelomanana, P. (2015). Indole alkaloids from the Marquesan plant Rauvolfia nukuhivensis and their effects on ion channels. Phytochemistry, 109, 84-95. doi:10.1016/j.phytochem.2014.10.026. [NMR235]

Morgenstern, A., Paetz, C., Behrend, A., Spiteller, D. (2015). Divalent transition-metal-ion stress induces Prodigiosin biosynthesis in Streptomyces coelicolor M145: formation of Coeligiosins. Chemistry – A European Journal, 21(16), 6027-6032. doi:10.1002/chem.201405733. [BOL619]

Poreddy, S., Mitra, S., Schöttner, M., Chandran, J. N., Schneider, B., Baldwin, I. T., Kumar, P., Pandit, S. S. (2015). Detoxification of hostplant’s chemical defense rather than its anti-predator co-option drives beta-glucosidase-mediated lepidopteran counter-adaptation. Nature Communications, 6: 8525. doi:10.1038/ncomms9525. [ITB506]

Schläger, S., Beran, F., Groot, A. T., Ulrichs, C., Veit, D., Paetz, C., Karumuru, B. R. M., Srinivasan, R., Schreiner, M., Mewis, I. (2015). Pheromone blend analysis and cross-attraction among populations of Maruca vitrata from Asia and West Africa. Journal of Chemical Ecology, 41, 1155-1162. doi:10.1007/s10886-015-0653-z. [BER003]

Shokoohinia, Y., Sajjadi, S.-E., Jassbi, A. R., Moradi, H., Ghassemi, N., Schneider, B. (2015). Sesquiterpenes and flavonoids of Anthemis odontostephana var. odontostephana. Chemistry of Natural Compounds, 51(3), 491-494. doi:10.1007/s10600-015-1322-8. [NMR220]

Zenger, K., Agnolet, S., Schneider, B., Kraus, B. (2015). Biotransformation of flavokawains A, B and C, chalcones from Kava (Piper methysticum), by human liver microsomes. Journal of Agricultural and Food Chemistry, 63(28), 6376-6385. doi:10.1021/acs.jafc.5b01858. [NMR219]

2014

Falk, K., Kästner, J., Bodenhausen, N., Schramm, K., Paetz, C., G. Vassão, D., Reichelt, M., von Knorre, D., Bergelson, J., Erb, M., Gershenzon, J., Meldau, S. (2014). The role of glucosinolates and the jasmonic acid pathway in resistance of Arabidopsis thaliana against molluskan herbivores. Molecular Ecology, 23(5), 1188-1203. doi:10.1111/mec.12610. [GER357]

Fang, J., Schneider, B. (2014). Laser microdissection: a sample preparation technique for plant micrometabolic profiling. Phytochemical Analysis, 25, 307-313. doi:10.1002/pca.2477. [NMR202]

Hammerbacher, A., Paetz, C., Wright, L., Fischer, T. C., Bohlmann, J., Davis, A. J., Fenning, T. M., Gershenzon, J., Schmidt, A. (2014). Flavan-3-ols in Norway spruce: Biosynthesis, accumulation and function in response to attack by the bark beetle-associated fungus Ceratocystis polonica. Plant Physiology, 164, 2107-2122. doi:10.1104/pp.113.232389. [GER379]

Hölscher, D., Dhakshinamoorthy, S., Alexandrov, T., Becker, M., Bretschneider, T., Bürkert, A., Crecelius, A. C., De Waele, D., Elsen, A., Heckel, D. G., Heklau, H., Hertweck, C., Kai, M., Knop, K., Krafft, C., Maddula, R. K., Matthäus, C., Popp, J., Schneider, B., Schubert, U., Sikora, R., Svatoš, A., Swennen, R. (2014). Phenalenone-type phytoalexins mediate resistance of banana plants (Musa spp.) to the burrowing nematode Radopholus similis. Proceedings of the National Academy of Sciences of the United States of America, 111(1), 105-110. doi:10.1073/pnas.1314168110. [NMR205]

Keller-Costa, T., Hubbard, P. C., Paetz, C., Nakamura, Y., da Silva, J. P., Rato, A., Barata, E. N., Schneider, B., Canario, A. V. M. (2014). Identity of a tilapia pheromone released by dominant males that primes females for reproduction. Current Biology, 24(18), 2130-2135. doi:10.1016/j.cub.2014.07.049. [NMR212]

Kia, S. H., Schulz, M., Ayah, E., Schouten, A., Müllenborn, C., Paetz, C., Schneider, B., Hofmann, D., Disko, U., Tabaglio, V., Marocco, A. (2014). Abutilon theophrasti’s defense against the allelochemical benzoxazolin-2(3H)-one: support by Actinomucor elegans. Journal of Chemical Ecology, 40(11-12), 1286-1298. doi:10.1007/s10886-014-0529-7. [NMR215]

Monakhova, Y., Schneider, B. (2014). The intramolecular Diels-Alder reaction of diarylheptanoids – quantum chemical calculation of structural features favoring the formation of phenylphenalenones. Molecules, 19, 5231-5242. doi:10.3390/molecules19045231. [NMR208]

Nagel, R., Berasategui, A., Paetz, C., Gershenzon, J., Schmidt, A. (2014). Overexpression of an isoprenyl diphosphate synthase in spruce leads to unexpected terpene diversion products that function in plant defense. Plant Physiology, 164(2), 555-569. doi:10.1104/pp.113.228940. [GER356]

Nakamura, Y., Paetz, C., Brandt, W., David, A., Rendón-Anaya, M., Herrera-Estrella, A., Mithöfer, A., Boland, W. (2014). Synthesis of 6-substituted 1-oxoindanoyl isoleucine conjugates and modeling studies with the COI1-JAZ co-receptor complex of lima bean. Journal of Chemical Ecology, 40, 687-699. doi:10.1007/s10886-014-0469-2. [BOL601]

Ramsay, A., Fliniaux, O., Fang, J., Molinie, R., Roscher, A., Grand, E., Guillot, X., Kovensky, J., Fliniaux, M.-A., Schneider, B., Mesnard, F. (2014). Development of an NMR metabolomics-based tool for selection of flaxseed varieties. Metabolomics, 10, 1258-1267. doi:10.1007/s11306-014-0664-8. [NMR207]

Rasool, A., Joußen, N., Lorenz, S., Ellinger, R., Schneider, B., Khan, S. A., Ashfaq, M., Heckel, D. G. (2014). An independent occurrence of the chimeric P450 enzyme CYP337B3 of Helicoverpa armigera confers cypermethrin resistance in Pakistan. Insect Biochemistry and Molecular Biology, 53, 54-65. doi:10.1016/j.ibmb.2014.07.006. [HEC282]

Schneider, B. (2014). Chemical Ecology. In M. J. Simpson, A. J. Simpson (Eds.), NMR Spectroscopy: A Versatile Tool for Environmental Research (pp. 223-242). Chichester, UK: John Wiley & Sons Ltd. [NMR210]

Tatsis, E., Eylert, E., Maddula, R. K., Ostrozhenkova, E., Svatoš, A., Eisenreich, W., Schneider, B. (2014). Biosynthesis of nudicaulins. A ¹³CO₂-pulse/chase labeling study with Papaver nudicaule. Chembiochem, 15, 1645-1650. doi:10.1002/cbic.201402109. [NMR209]

2013

Besseau, S., Kellner, F., Lanoue, A., Thamm, A. M., Salim, V., Schneider, B., Geu-Flores, F., Höfer, R., Guirimand, G., Guihur, A., Oudin, A., Glevarec, G., Foureau, E., Papon, N., Clastre, M., Giglioli-Guivarc’h, N., St-Pierre, B., Werck-Reichhart, D., Burlat, V., Luca, V. D., O'Connor, S. E., Courdavault, V. (2013). A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ dependent manner in Catharanthus roseus. Plant Physiology, 163(4), 1792-1803. doi:10.1104/pp.113.222828. [NMR203]

Buch, F., Rott, M., Rottloff, S., Paetz, C., Hilke, I., Raessler, M., Mithöfer, A. (2013). Secreted pitfall-trap fluid of carnivorous Nepenthes plants is unsuitable for microbial growth. Annals of Botany, 111(3), 375-383. doi:10.1093/aob/mcs287. [BOL551]

de Souza, G. D., Mithöfer, A., Daolio, C., Schneider, B., Rodrigues-Filho, E. (2013). Identification of Alternaria alternata mycotoxins by LC-SPE-NMR and their cytotoxic effects to soybean (Glycine max) cell suspension culture. Molecules and Cells, 18, 2528-2538. doi:10.3390/molecules18032528. [BOL556]

Duque, L., Zapata, C., Rojano, B., Schneider, B., Otalvaro, F. (2013). Radical scavenging capacity of 2,4-dihydroxy-9-phenyl-1H-phenalen-1-one: A functional group exclusion approach. Organic Letters, 15(14), 3542-3545. doi:10.1021/ol400384z. [NMR201]

Fang, J., Ramsay, A., Paetz, C., Tatsis, E., Renouard, S., Hano, C., Grand, E., Fliniaux, O., Roscher, A., Mesnard, F., Schneider, B. (2013). Concentration kinetics of secoisolariciresinol diglucoside and its biosynthetic precursor coniferin in developing flaxseed. Phytochemical Analysis, 24(1), 41-46. doi:10.1002/pca.2377. [NMR188]

Ginglinger, J.-F., Boachon, B., Höfer, R., Paetz, C., Köllner, T., Lugan, R., Mutterer, J., Fischer, M., Ullmann, P., Beran, F., Claudel, P., Baltenweck, R., Miesch, L., Verstappen, F., Bouwmeester, H., Miesch, M., Schneider, B., Gershenzon, J., Ehlting, J., Werck-Reichhart, D. (2013). Gene coexpression analysis reveals a complex metabolism of the monoterpene alcohol linalool in Arabidopsis flowers. The Plant Cell, 25(11), 4640-4657. doi:10.1105/tpc.113.117382. [GER362]

Hammerbacher, A., Schmidt, A., Wadke, N., Wright, L., Schneider, B., Bohlmann, J., Brand, W., Fenning, T. M., Gershenzon, J., Paetz, C. (2013). A common fungal associate of the spruce bark beetle metabolizes the stilbene defenses of Norway spruce. Plant Physiology, 162, 1324-1336. doi:10.1104/pp.113.218610. [GER344]

Happyana, N., Agnolet, S., Muntendam, R., van Dam, A., Schneider, B., Kayser, O. (2013). Analysis of cannabinoids in laser-microdissected trichomes of medicinal Cannabis sativa using LCMS and cryogenic NMR. Phytochemistry, 87, 51-59. doi:10.1016/j.phytochem.2012.11.001. [NMR196]

Heinrich, M., Hettenhausen, C., Lange, T., Wünsche, H., Fang, J., Baldwin, I. T., Wu, J. (2013). High levels of jasmonic acid antagonize the biosynthesis of gibberellins and inhibit the growth of Nicotiana attenuata stems. The Plant Journal, 73(4), 591-606. doi:10.1111/tpj.12058. [ITB397]

Irmisch, S., Clavijo McCormick, A. L., Boeckler, A., Schmidt, A., Reichelt, M., Schneider, B., Block, K., Schnitzler, J.-P., Gershenzon, J., Unsicker, S., Köllner, T. (2013). Two herbivore-induced cytochrome P450 enzymes CYP79D6 and CYP79D7 catalyze the formation of volatile aldoximes involved in poplar defense. The Plant Cell, 25(11), 4737-4754. doi:10.1105/tpc.113.118265. [GER361]

Kunert, M., Rahfeld, P., Shaker, K. H., Schneider, B., David, A., Dettner, K., Pasteels, J. M., Boland, W. (2013). Beetles do it differently: Two stereodivergent cyclisation modes in iridoid-producing leaf-beetle larvae. ChemBioChem, 14, 353-360. doi:10.1002/cbic.201200689. [BOL561]

Li, C.-H., Jing, S.-X., Luo, S.-H., Shi, W., Hua, J., Liu, Y., Li, X.-N., Schneider, B., Gershenzon, J., Li, S.-H. (2013). Peltate glandular trichomes of Colquhounia coccinea var. Mollis Harbor a new class of defensive sesterterpenoids. Organic Letters, 15(7), 1694-1697. doi:10.1021/ol4004756. [GER342]

Miosic, S., Knop, K., Hölscher, D., Greiner, J., Gosch, C., Thill, J., Kai, M., Shrestha, B. K., Schneider, B., Crecelius, A. C., Schubert, U. S., Svatoš, A., Stich, K., Halbwirth, H. (2013). 4-Deoxyaurone formation in Bidens ferulifolia (Jacq.) DC. PLoS One, 8(5): e61766. doi:10.1371/journal.pone.0061766. [MS147]

Munde, T., Brand, S., Hidalgo, W., Maddula, R. K., Svatoš, A., Schneider, B. (2013). Biosynthesis of tetraoxygenated phenylphenalenones in Wachendorfia thyrsiflora. Phytochemistry, 91, 165-176. doi:10.1016/j.phytochem.2012.02.020. [NMR187]

Pardo-Torre, J., Schmidt, G., Paetz, C., Reichelt, M., Schneider, B., Gershenzon, J., D'Auria, J. (2013). The biosynthesis of hydroxycinnamoyl quinate esters and their role in the storage of cocaine in Erythroxylum coca. Phytochemistry, 91, 177-186. doi:10.1016/j.phytochem.2012.09.009. [GER346]

Schneider, B. (2013). Chemical Ecology. In R. K. Harris, R. E. Wasylishen (Eds.), eMagRes (pp. 451-466). John Wiley and Sons. doi:10.1002/9780470034590.emrstm1341. [NMR204]

Soh, D., Nkwengoua, E., Ngantchou, I., Nyasse, B., Denier, C., Hannaert, V., Shaker, K. H., Schneider, B. (2013). Xylopioxyde and other bioactive kaurane-diterpenes from Xylopia aethiopica Dunal (Annonaceae). Journal of Applied Pharmaceutical Science, 3(12), 013-019. [NMR206]

Tatsis, E., Böhm, H., Schneider, B. (2013). Occurrence of nudicaulin structural variants in flowers of papaveraceous species. Phytochemistry, 105-112. doi:10.1016/j.phytochem.2013.04.011. [NMR200]

Tatsis, E., Schaumlöffel, A., Warskulat, A.-C., Massiot, G., Schneider, B., Bringmann, G. (2013). Nudicaulins, yellow flower pigments of Papaver nudicaule: Revised constitution and assignment of absolute configuration. Organic Letters, 15(1), 156-159. doi:10.1021/ol303211w. [NMR198]

2012

Baranovsky, A. V., Bolibrukh, D. A., Khripach, V. A., Schneider, B. (2012). Diels–Alder reaction of androsta-14,16-dien-17-yl acetates with nitroethylene: Product distribution and selected adduct transformations. Steroids, 78, 282-287. doi:10.1016/j.steroids.2012.11.015. [NMR199]

Cano, M., Rojas, C., Hidalgo, W., Sáez, J., Gil, J., Schneider, B., Otálvaro, F. (2012). Improved synthesis of 4-phenylphenalenones: the case of isoanigorufone and structural analogs. Tetrahedron Letters, 54, 351-354. doi:10.1016/j.tetlet.2012.11.118. [NMR197]

Cervellati, C., Paetz, C., Dondini, L., Tartarini, S., Bassi, D., Schneider, B., Masia, A. (2012). A qNMR approach for bitterness phenotyping and QTL identification in an F1 apricot progeny. Journal of Biotechnology, 159, 312-319. doi:10.1016/j.jbiotec.2011.09.004. [NMR185]

Daolio, C., Schneider, B. (2012). Coupling liquid chromatography and other separation techniques to nuclear magnetic resonance spectroscopy. In Hyphenated and Alternative Methods of Detection in Chromatography (pp. 61-98). [NMR184]

Docimo, T., Reichelt, M., Schneider, B., Kai, M., Kunert, G., Gershenzon, J., D'Auria, J. (2012). The first step in the biosynthesis of cocaine in Erythroxylum coca: the characterization of arginine and ornithine decarboxylases. Plant Molecular Biology, 78(6), 599-615. doi:10.1007/s11103-012-9886-1. [GER321]

Fang, J., Hölscher, D., Schneider, B. (2012). Co-occurrence of phenylphenalenones and flavonoids in Xiphidium caeruleum Aubl. flowers. Phytochemistry, 82, 143-148. doi:10.1016/j.phytochem.2012.07.005. [NMR192]

Fang, J., Kai, M., Schneider, B. (2012). Phytochemical profile of aerial parts and roots of Wachendorfia thyrsiflora L. studied by LC-DAD-SPE-NMR. Phytochemistry, 81, 144-152. doi:10.1016/j.phytochem.2012.05.023. [NMR190]

Fang, J., Reichelt, M., Hidalgo, W., Agnolet, S., Schneider, B. (2012). Tissue-specific distribution of secondary metabolites in rapeseed (Brassica napus). PLoS One, 7(10): e48006. doi:10.1371/journal.pone.0048006. [NMR194]

Fang, J., Reichelt, M., Kai, M., Schneider, B. (2012). Metabolic profiling of lignans and other secondary metabolites from rapeseed (Brassica napus L.). Journal of Agricultural and Food Chemistry, 60, 10523-10529. doi:10.1021/jf303907b. [NMR193]

Iranshahi, M., Amanolahi, F., Schneider, B. (2012). New sesquiterpene coumarin from the roots of Ferula latisecta. Avicenna Journal of Phytomedicine, 2(3), 133-138. [NMR191]

Jirschitzka, J., Schmidt, G., Reichelt, M., Schneider, B., Gershenzon, J., D'Auria, J. (2012). Plant tropane alkaloid biosynthesis evolved independently in the Solanaceae and Erythroxylaceae. Proceedings of the National Academy of Sciences of the United States of America, 109(26), 10304-10309. doi:10.1073/pnas.1200473109. [GER328]

Joußen, N., Agnolet, S., Lorenz, S., Schöne, S. E., Ellinger, R., Schneider, B., Heckel, D. G. (2012). Resistance of Australian Helicoverpa armigera to fenvalerate is due to the chimeric P450 enzyme CYP337B3. Proceedings of the National Academy of Sciences of the United States of America, 109(38), 15206-15211. doi:10.1073/pnas.1202047109. [HEC230]

Kaur, H., Shaker, K. H., Heinzel, N., Ralph, J., Galis, I., Baldwin, I. T. (2012). Environmental stresses of field growth allow cinnamyl alcohol dehydrogenase-deficient Nicotiana attenuata plants to compensate for their structural deficiencies. Plant Physiology, 159(4), 1545-1570. doi:10.1104/pp.112.196717. [ITB374]

Krafft, C., Cervellati, C., Paetz, C., Schneider, B., Popp, J. (2012). Distribution of amygdalin in apricot (Prunus armeniaca) seeds studied by Raman microscopic imaging. Applied Spectroscopy, 66(6), 644-649. doi:10.1366/11-06521. [NMR189]

Li, S.-H., Nagy, N. E., Hammerbacher, A., Krokene, P., Niu, X.-M., Gershenzon, J., Schneider, B. (2012). Localization of phenolics in phloem parenchyma cells of Norway spruce (Picea abies). ChemBioChem: A European Journal of Chemical Biology, 13, 2707-2713. doi:10.1002/cbic.201200547. [NMR195]

Luo, S.-H., Liu, Y., Hua, J., Niu, X.-M., Jing, S.-X., Zhao, X., Schneider, B., Gershenzon, J., Li, S.-H. (2012). Unique proline-benzoquinone pigment from the colored nectar of “Bird’s Coca Cola Tree” functions in bird attractions. Organic Letters, 14(16), 4146-4149. doi:10.1021/ol3017879. [GER319]

Schoenian, I., Paetz, C., Dickschat, J. S., Aigle, B., Leblond, P., Spiteller, D. (2012). An unprecedented 1,2-shift in the biosynthesis of the 3-aminosalicylate moiety of antimycins. ChemBioChem, 13(6), 769-773. doi:10.1002/cbic.201200033. [BOL523]

Yan, Y.-M., Dai, H.-Q., Du, Y., Schneider, B., Guo, H., Li, D.-P., Zhang, L.-X., Fu, H., Dong, X.-P., Cheng, Y.-X. (2012). Identification of blapsins A and B as potent small-molecule 14-3-3 inhibitors from the insect Blaps japanensis. Bioorganic & Medicinal Chemistry Letters, 22(12), 4179-4181. doi:10.1016/j.bmcl.2012.04.027. [NMR186]

2011

Ahn, S.-J., Badenes-Pérez, F. R., Reichelt, M., Svatoš, A., Schneider, B., Gershenzon, J., Heckel, D. G. (2011). Metabolic detoxification of capsaicin by UDP-glycosyltransferase in three Helicoverpa species. Archives of Insect Biochemistry and Physiology, 78(2), 104-118. doi:10.1002/arch.20444. [HEC198]

Berg, A., Wyrwa, R., Weisser, J., Weiss, T., Schade, R., Hildebrand, G., Liefeith, K., Schneider, B., Ellinger, R., Schnabelrauch, M. (2011). Synthesis of photopolymerizable hydrophilic macromers and evaluation of their applicability as reactive resin components for the fabrication of three-dimensionally structured hydrogel matrices by 2-photon-polymerization. Advanced Engineering Materials, 13(9), B274-B284. doi:10.1002/adem.201080092. [NMR144]

Fang, J., Paetz, C., Hölscher, D., Munde, T., Schneider, B. (2011). Phenylphenalenones and related natural products from Wachendorfia thyrsiflora L. Phytochemistry Letters, 4(2), 203-208. doi:10.1016/j.phytol.2011.03.006. [NMR181]

Fang, J., Paetz, C., Schneider, B. (2011). C-methylated flavanones and dihydrochalcones from Myrica gale seeds. Biochemical Systematics and Ecology, 39(1), 68-70. doi:10.1016/j.bse.2011.01.009. [NMR095]

Frölich, N., Dees, C., Paetz, C., Ren, X., Lohse, M. J., Nikolaev, V. O., Zenk, M. H. (2011). Distinct pharmacological properties of morphine metabolites at Gi-protein and b-arrestin signaling pathways activated by the human m-opioid receptor. Biochemical Pharmacology, 81(10), 1248-1254. doi:10.1016/j.bcp.2011.03.001. [NMR165]

Morad, S. A., Schmidt, C., Büchele, B., Schneider, B., Wenzler, M., Syrovets, T., Simmet, T. (2011). (8R)-3ß,8-Dihydroxypolypoda-13E,17E,21-triene induces cell cycle arrest and apoptosis in treatment-resistant prostate cancer cells. Journal of Natural Products, 74, 1731-1736. doi:10.1021/np200161a. [NMR183]

Munde, T., Maddula, R. K., Svatoš, A., Schneider, B. (2011). The biosynthetic origin of oxygen functions in phenylphenalenones of Anigozanthos preissii inferred from NMR- and HRMS-based isotopologue analysis. Phytochemistry, 72, 49-58. doi:10.1016/j.phytochem.2010.10.007. [NMR118]

Nganso, Y. O. D., Ngantchou, I. E. W., Nkwenoua, E., Nyasse, B., Denier, C., Hannert, V., Schneider, B. (2011). Preparation antitrypanosomal and cytotoxic activities of 22-hydroxyclerosterol, a new sterol from Allexis cauliflora (Violaceae). Scientia Pharmaceutica, 79(1), 137-144. doi:10.3797/scipharm.1012-10. [NMR154]

Rempt, M., Schneider, B., Pohnert, G. (2011). A reactive conjugated allene involved in the biosynthesis of volatile oxylipins in the moss Dicranum scoparium. Organic Letters, 13, 3229-3231. doi:10.1021/ol201114g. [NMR182]

Schneider, B. (2011). Nuclear magnetic resonance spectroscopic analysis of enzyme products. Progress in Botany, 72, 183-208. doi:10.1007/978-3-642-13145-5_7. [NMR115]

Shao, Y., Spiteller, D., Tang, X., Ping, L., Colesie, C., Münchberg, U., Bartram, S., Schneider, B., Büdel, B., Popp, J., Heckel, D. G., Boland, W. (2011). Crystallization of a- and ß-carotene in the foregut of Spodoptera larvae feeding on a toxic food plant. Insect Biochemistry and Molecular Biology, 41(4), 273-281. doi:10.1016/j.ibmb.2011.01.004. [BOL506]

Weinhold, A., Shaker, K. H., Wenzler, M., Schneider, B., Baldwin, I. T. (2011). Phaseoloidin, a homogentisic acid glucoside from Nicotiana attenuata trichomes, contributes to the plant’s resistance against Lepidopteran herbivores. Journal of Chemical Ecology, 37, 1091-1098. doi:10.1007/s10886-011-0012-7. [ITB333]

Ziaei, A., Ramezani, M., Wright, L., Paetz, C., Schneider, B., Amirghofran, Z. (2011). Identification of spathulenol in Salvia mirzayanii and the immunomodulatory effects. Phytotherapy Research, 25(4), 557-562. doi:10.1002/ptr.3289. [NMR153]

2010

Bartsch, M., Bednarek, P., Vivancos, P. D., Schneider, B., von Röpenack-Lahaye, E., Foyer, C., Kombrink, E., Scheel, D., Parker, J. E. (2010). Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-ß-D-xyloside in Arabidopsis resistance to pathogens and ageing of leaves. The Journal of Biological Chemistry, 285, 25654-25665. doi:10.1074/jbc.M109.092569. [NMR114]

Bürkert, A., Khanjari, S. A., Al-Saady, N. A., De Langhe, E., Hölscher, D., Gebauer, J., Behrendt, S., Happe, S., Brinkmann, K., Schlecht, E. (2010). Wie sich Oasen-Bananen gegen ihre Feinde wehren. Uralter Toleranzmechanismus im Oman entdeckt. Biologie in unserer Zeit, 40(5), 334-341. doi:10.1002/biuz.201010432. [NMR119]

Dagvadorj, E., Shaker, K. H., Windsor, D., Schneider, B., Boland, W. (2010). Phenolic glucosides from Hasseltia floribunda. Phytochemistry, 71(16), 1900-1907. doi:10.1016/j.phytochem.2010.08.004. [BOL409]

Drach, S., Khripach, V., Litvinovskaya, R., Lyakhov, A., Schneider, B., Zhylitskaya, H. (2010). Stereoselective synthesis of 9a-hydroxylated ecdysteroids. Steroids, 75(2), 184-188. doi:10.1016/j.steroids.2009.10.011. [NMR094]

Duque, L., Restrepo, C., Sáez, J., Gil, J., Schneider, B., Otálvaro, F. (2010). Synthesis of musafluorone: A naphthoxanthenone isolated from Musa acuminata. Tetrahedron Letters, 51(35), 4640-4643. doi:10.1016/j.tetlet.2010.06.128. [NMR116]

Gosch, C., Halbwirth, H., Schneider, B., Hölscher, D., Stich, K. (2010). Cloning and heterologous expression of glycosyltransferases from Malus x domestica and Pyrus communis, which convert phloretin to phloretin 2'-O-glucoside (phloridzin). Plant Science, 178(3), 299-306. doi:10.1016/j.plantsci.2009.12.009. [NMR180]

Heiling, S., Schuman, M. C., Schöttner, M., Mukerjee, P., Berger, B., Schneider, B., Jassbi, A., Baldwin, I. T. (2010). Jasmonate and ppHsystemin regulate key malonylation steps in the biosynthesis of 17-hydroxygeranyllinalool diterpene glycosides, an abundant and effective direct defense against herbivores in Nicotiana attenuata. The Plant Cell, 22(1), 273-292. doi:10.1105/tpc.109.071449. [ITB140]

Iranshahi, M., Kalategi, F., Sahebkar, A., Sardashti, A., Schneider, B. (2010). New sesquiterpene coumarins from the roots of Ferula flabelliloba. Pharmaceutical Biology, 48(2), 217-220. doi:10.3109/13880200903019226. [NMR093]

Jitsaeng, K., Paetz, C., Schneider, B. (2010). Phenylphenalenones from Musa cv. 'Thepanom' (BBB). Records of Natural Products, 4(1), 26-30. [NMR065]

Jitsaeng, K., Schneider, B. (2010). Metabolic profiling of Musa acuminata challenged with Sporobolomyces salmonicolor. Phytochemistry Letters, 3(2), 84-87. doi:10.1016/j.phytol.2010.02.001. [NMR099]

Khripach, V., Zhabinskii, V., Zhiburtovich, Y., Ivanova, G., Konstantinova, O., Tsavlovskii, D., Lorenz, S., Schneider, B. (2010). Preparation and synthetic application of partially protected brassinosteroids. Steroids, 75(1), 27-33. doi:10.1016/j.steroids.2009.09.010. [NMR179]

Kroiß, J., Kaltenpoth, M., Schneider, B., Schwinger, M.-G., Hertweck, C., Maddula, R. K., Strohm, E., Svatos, A. (2010). Symbiotic streptomycetes provide antibiotic combination prophylaxis for wasp offspring. Nature Chemical Biology, 6, 261-263. doi:10.1038/nchembio.331. [KAL001]

Luo, S.-H., Luo, Q., Niu, X., Xie, M.-J., Zhao, X., Schneider, B., Gershenzon, J., Li, S.-H. (2010). Glandular trichomes of Leucosceptrum canum harbor defensive sesterterpenoids. Angewandte Chemie International Edition, 49, 4471-4475. doi:10.1002/ange.201000449. [GER280]

Ngantchou, I., Nyasse, B., Denier, C., Blonski, C., Hannaert, V., Schneider, B. (2010). Antitrypanosomal alkaloids from Polyalthia suaveolens (Annonaceae): their effects on three selected glycolytic enzymes of Trypanosoma brucei. Bioorganic & Medicinal Chemistry Letters, 20(12), 3495-3498. doi:10.1016/j.bmcl.2010.04.145. [NMR112]

Otálvaro, F., Jitsaeng, K., Munde, T., Echeverri, F., Quinones, W., Schneider, B. (2010). O-Methylation of phenylphenalenone phytoalexins in Musa acuminata and Wachendorfia thyrsiflora. Phytochemistry, 71(2-3), 206-213. doi:10.1016/j.phytochem.2009.10.019. [NMR177]

Shaker, K. H., Morsy, N., Zinecker, H., Imhoff, J., Schneider, B. (2010). Secondary metabolites from Calotropis procera (Aiton). Phytochemistry Letters, 3(4), 212-216. doi:10.1016/j.phytol.2010.07.009. [NMR117]

Shaker, K., Zinecker, H., Ghani, M., Imhoff, J., Schneider, B. (2010). Bioactive metabolites from the sponge Suberea sp. Chemistry and Biodiversity, 7(12), 2880-2887. doi:10.1002/cbdv.200900277. [NMR096]

2009

Bednarek, P., Pislewska-Bednarek, M., Svatos, A., Schneider, B., Doubský, J., Mansourova, M., Humphry, M., Consonni, C., Panstruga, R., Sanchez-Vallet, A., Molina, A., Schulze-Lefert, P. (2009). A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense. Science, 323, 101-106. [MS128]

Hidalgo, W., Duque, L., Saez, J., Arango, R., Gil, J., Rojano, B., Schneider, B., Otálvaro, F. (2009). Structure-activity relationship in the interaction of substituted perinaphthenones with Mycosphaerella fijiensis. Journal of Agricultural and Food Chemistry, 57(16), 7417-7421. doi:10.1021/jf901052e. [NMR176]

Hölscher, D., Shroff, R., Knop, K., Gottschaldt, M., Crecelius, A., Schneider, B., Heckel, D. G., Schubert, U. S., Svatos, A. (2009). Matrix-free UV-laser desorption/ionization (LDI) mass spectrometric imaging at the single-cell level: Distribution of secondary metabolites of Arabidopsis thaliana and Hypericum species. The Plant Journal, 60(5), 907-918. doi:10.1111/j.1365-313X.2009.04012.x. [MS118]

Iranshahi, M., Noroozi, A., Behravan, J., Karimi, G., Schneider, B. (2009). Persicasulphide C, a new sulphur-containing derivative from Ferula persica. Natural Product Research, 23(17), 1584-1588. doi:10.1080/14786410802393571. [NMR178]

Jean, T. P., Shaari, K., Paetz, C., Ismail, I. S., Abas, F., Lajis, N. H., Ahmad, V. U. (2009). Bidesmosidic oleanane saponins from Xerospermum noronhianum. Helvetica Chimica Acta, 92(10), 1973-1982. doi:10.1002/hlca.200900063. [NMR019]

Jitsaeng, K., De Eknamkul, W., Schneider, B. (2009). Flavonoids and a new calamenene-type sesquiterpene from rhizomes of Alpinia oxymitra K. Schum (Zingiberaceae). Records of Natural Products, 3(2), 110-113. [NMR171]

Knill, T., Reichelt, M., Paetz, C., Gershenzon, J., Binder, S. (2009). Arabidopsis thaliana encodes a bacterial-type heterodimeric isopropylmalate isomerase involved in both Leu biosynthesis and the Met chain elongation pathway of glucosinolate formation. Plant Molecular Biology Reporter, 71(3), 227-239. doi:10.1007/s11103-009-9519-5. [GER269]

Larbat, R., Hehn, A., Hans, J., Schneider, S., Jugdé, H., Schneider, B., Matern, U., Bourgaud, F. (2009). Isolation and functional characterization of CYP71AJ4 encoding for the first P450 monooxygenase of angular furanocoumarin biosynthesis. The Journal of Biological Chemistry, 284(8), 4776-4785. doi:10.1074/jbc.M807351200. [NMR168]

Lusebrink, I., Dettner, K., Schierling, A., Müller, T., Daolio, C., Schneider, B., Schmidt, J., Seifert, K. (2009). New pyridine alkaloids from rove beetles of the genus Stenus (Coleoptera: Staphylinidae). Zeitschrift für Naturforschung, C: Journal of Biosciences, 64(3-4), 271-278. doi:10.1515/znc-2009-3-420. [NMR172]

Maulidiani, Shaari, K., Paetz, C., Stanslas, J., Abas, F., Lajis, N. H. (2009). Naturally occurring labdane diterpene and benzofuran from Globba pendula. Natural Product Communications, 4(8), 1031-1036. doi:10.1177/1934578X0900400803. [NMR017]

Moco, S., Schneider, B., Vervoort, J. (2009). Plant micrometabolomics: the analysis of endogenous metabolites present in a plant cell or tissue. Journal of Proteome Research, 8(4), 1694-1703. doi:10.1021/pr800973r. [NMR170]

Ngantchou, I., Nkwengoua, E., Nganso, Y., Nyasse, B., Denier, C., Hannaert, V., Schneider, B. (2009). Antitrypanosomal activity of polycarpol from Piptostigma preussi (Annonaceae). Fitoterapia, 80(3), 188-191. doi:10.1016/j.fitote.2009.01.008. [NMR169]

Nkwengoua, E., Ngantchou, I., Nyasse, B., Denier, C., Blonski, C., Schneider, B. (2009). in vitro inhibitory effects of palmatine from Enantia chlorantha on Trypanosoma cruzi and Leishmania infantum. Natural Product Research, 23(12), 1144-1150. doi:10.1080/14786410902726241. [NMR175]

Nyasse, B., Nono, J.-J., Nganso, Y., Ngantchou, I., Schneider, B. (2009). Uapaca genus (Euphorbiaceae), a good source of betulinic acid. Fitoterapia, 80(1), 32-34. doi:10.1016/j.fitote.2008.09.005. [NMR167]

2008

Abdullah, Y., Schneider, B., Petersen, M. (2008). Occurrence of rosmarinic acid, chlorogenic acid and rutin in Marantaceae species. Phytochemistry Letters, 1, 199-203. doi:10.1016/j.phytol.2008.09.010. [NMR174]

Baranovsky, A. V., Bolibrukh, D. A., Khripach, V. A., Schneider, B. (2008). A new approach to heterocycle-modified steroids via nitrile oxide intermediates. Arkivoc, 9, 29-41. [NMR163]

Berim, A., Ebel, R., Schneider, B., Petersen, M. (2008). UDP-glucose:(6-methoxy)podophyllotoxin 7-O-glucosyltransferase from suspension cultures of Linum nodiflorum. Phytochemistry, 69(2), 374-381. doi:10.1016/j.phytochem.2007.07.030. [NMR159]

Hölscher, D., Brand, S., Wenzler, M., Schneider, B. (2008). NMR-based metabolic profiling of Anigozanthos floral nectar. Journal of Natural Products, 71(2), 251-257. doi:10.1021/np0705514. [NMR173]

Hölscher, D., Schneider, B. (2008). Application of laser-assisted microdissection for tissue and cell-specific analysis of RNA, proteins, and metabolites. Progress in Botany, 69, 141-167. doi:10.1007/978-3-540-72954-9_6. [NMR157]

Iranshahi, M., Mojarab, M., Sadeghian, H., Hanafi-Bojd, M. Y., Schneider, B. (2008). Polar secondary metabolites of Ferula persica roots. Phytochemistry, 69(2), 473-478. doi:10.1016/j.phytochem.2007.08.001. [NMR155]

Khripach, V., Zhabinskii, V. N., Fando, G. P., Khripach, N. B., Schneider, B. (2008). Synthesis and radical oxidation of steroidal 1-oxo-5-alpha-alcohols. ARKIVOC, 9, 20-28. doi:10.3998/ark.5550190.0009.903. [NMR162]

Khripach, V., Zhabinskii, V., Antonchick, A., Litvinovskaya, R., Drach, S., Sviridov, O., Pryadko, A., Novik, T., Matveentsev, V., Schneider, B. (2008). A new type of modified brassinosteroids for enzyme-linked immunosorbent assay. Natural Product Communications, 3(5), 735-748. doi:10.1177/1934578X0800300513. [NMR160]

Köllner, T. G., Schnee, C., Li, S., Svatos, A., Schneider, B., Gershenzon, J., Degenhardt, J. (2008). Protonation of a neutral (S)-beta-bisabolene intermediate is involved in (S)-beta-macrocarpene formation by the maize sesquiterpene synthases TPS6 and TPS11. The Journal of Biological Chemistry, 283(30), 20779-20788. doi:10.1074/jbc.M802682200. [GER245]

Li, S. H., Niu, X. M., Zahn, S., Gershenzon, J., Weston, J., Schneider, B. (2008). Diastereomeric stilbene glucoside dimers from the bark of Norway spruce (Picea abies). Phytochemistry, 69(3), 772-782. [NMR156]

Murgu, M., Santos, A., Souza, D., Daolio, C., Schneider, B., Ferreira, A. G., Rodrigues-Filho, E. (2008). Hydroxylation of a hederagenin derived saponin by a xylareaceous fungus found in fruits of Sapindus saponaria. Journal of the Brazilian Chemical Society, 9, 831-835. doi:10.1590/S0103-50532008000500004. [NMR164]

Nanclares, J., Gil, J., Rojano, B., Saez, J., Schneider, B., Otalvaro, F. (2008). Synthesis of 4-methoxy-1H-phenalen-1-one: a subunit related to natural phenalenone-type compounds. Tetrahedron Letters, 49(24), 3844-3847. doi:10.1016/j.tetlet.2008.04.095. [NMR161]

Tao, Q. F., Xu, Y., Lam, R. Y. Y., Schneider, B., Dou, H., Leung, P. S., Shi, S. Y., Zhou, C. X., Yang, L. X., Zhang, R. P., Xiao, Y. C., Wu, X., Stöckigt, J., Zeng, S., Cheng, C. H. K., Zhao, Y. (2008). Diarylheptanoids and a monoterpenoid from the rhizomes of Zingiber officinale: antioxidant and cytoprotective properties. Journal of Natural Products, 71(1), 12-17. doi:10.1021/np070114p. [NMR158]

Vergara, F., Wenzler, M., Hansen, B. G., Kliebenstein, D. J., Halkier, B. A., Gershenzon, J., Schneider, B. (2008). Determination of the absolute configuration of the glucosinolate methyl sulfoxide group reveals a stereospecific biosynthesis of the side chain. Phytochemistry, 69(15), 2737-2742. doi:10.1016/j.phytochem.2008.09.008. [GER248]

Wenzler, M., Hölscher, D., Oerther, T., Schneider, B. (2008). Nectar formation and floral nectary anatomy of Anigozanthos flavidus - a combined magnetic resonance imaging and spectroscopy study. Journal of Experimental Botany, 59(12), 3425-3434. doi:10.1093/jxb/ern191. [NMR166]

2007

Berim, A., Schneider, B., Petersen, M. (2007). Methyl allyl ether formation in plants: novel S-adenosyl L-methionine:coniferyl alcohol 9-O-methyltransferase from suspension cultures of three Linum species. Plant Molecular Biology, 64(3), 279-291. doi:10.1007/s11103-007-9151-1. [NMR147]

Emami, S. A., Amin-Ar-Ramimeh, E., Ahi, A., Kashy, M. R. B., Schneider, B., Iranshahi, M. (2007). Prenylated flavonoids and flavonostilbenes from Sophora pachycarpa roots. Pharmaceutical Biology, 45(6), 453-457. doi:10.1080/13880200701389078. [NMR150]

Hemmati, S., Schneider, B., Schmidt, T., Federolf, K., Alfermann, A. W., Fuss, E. (2007). Justicidin B 7-hydroxylase, a cytochrome P450 monooxygenase from cell cultures of Linum perenne Himmelszelt involved in the biosynthesis of diphyllin. Phytochemistry, 68(22-24), 2736-2743. doi:10.1016/j.phytochem.2007.10.025. [NMR152]

Khripach, V. A., Khripach, N. B., Zhabinskii, V. N., Zhiburtovich, Y. Y., Schneider, B., Degroot, A. T. (2007). Synthesis of [7,7-2H2]epibrassinolide. Journal of Labelled Compounds and Radiopharmaceuticals, 50(13), 1153-1158. doi:10.1002/jlcr.1408. [NMR151]

Li, S. H., Schneider, B., Gershenzon, J. (2007). Microchemical analysis of laser-microdissected stone cells of Norway spruce by cryogenic nuclear magnetic resonance spectroscopy. Planta, 225(3), 771-779. doi:10.1007/s00425-006-0376-z. [NMR139]

Otalvaro, F., Nanclares, J., Estella, L., Quinones, W., Echeverri, W., Arango, R., Schneider, B. (2007). Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijensis. Journal of Natural Products, 70(5), 887-890. doi:10.1021/np070091e. [NMR148]

Schneider, B. (2007). Nuclear magnetic resonance spectroscopy in biosynthetic studies. Progress in Nuclear Magnetic Resonance Spectroscopy, 51(3), 155-198. doi:10.1016/j.pnmrs.2007.02.006. [NMR146]

Schneider, B., Hölscher, D. (2007). Laser microdissection and cryogenic nuclear magnetic resonance spectroscopy: an alliance for cell type-specific metabolite profiling. Planta, 225(3), 763-770. doi:10.1007/s00425-006-0404-z. [NMR141]

Vdovitchenko, M. Y., Kuzovkina, I. N., Paetz, C., Schneider, B. (2007). Formation of phenolic compounds in the roots of Hedysarum theinum cultured in vitro. Russian Journal of Plant Physiology, 54(4), 536-544. [NMR149]

2006

Antonchik, A. P., Svatos, A., Konstantinova, O. V., Zhabinskii, V. N., Khripach, V. A., Schneider, B. (2006). Reversible conversion in the brassinosteroid quartet castasterone, brassinolide and their 3 beta-epimers. Zeitschrift für Naturforschung, B: A Journal of Chemical Sciences, 61(8), 1039-1044. doi:10.1515/znb-2006-0817. [NMR138]

Brand, S., Holscher, D., Schierhorn, A., Svatos, A., Schroder, J., Schneider, B. (2006). A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis. Planta, 224(2), 413-428. doi:10.1007/s00425-006-0228-x. [NMR137]

Buchele, B., Zugmaier, W., Estrada, A., Genze, F., Syrovets, T., Paetz, C., Schneider, B., Simmet, T. (2006). Characterization of 3 alpha-acetyl-11-keto-alpha-boswellic acid, a pentacyclic triterpenoid inducing apoptosis in vitro and in vivo. Planta Medica, 72(14), 1285-1289. doi:10.1055/s-2006-951680. [NMR143]

Cheng, Y., Schneider, B., Riese, U., Schubert, B., Li, Z., Hamburger, M. (2006). (+)-N-deoxymillitarinone A, a neuritogenic pyridone alkaloid from the insect pathogenic fungus Paecilomyces farinosus. Journal of Natural Products, 69(3), 436-438. doi:10.1021/np050418g. [NMR135]

Hölscher, D., Reichert, M., Gorls, H., Ohlenschlager, O., Bringmann, G., Schneider, B. (2006). Monolaterol, the first configurationally assigned phenylphenalenone derivative with a stereogenic center at C-9, from Monochoria elata. Natural Product Reports, 69(11), 1614-1617. doi:10.1021/np060192x. [NMR142]

Nyasse, B., Ngantchou, I., Nono, J.-J., Schneider, B. (2006). Antifilarial activity in vitro of polycarpol and 3-O-acetyl aleuritolic acid from Cameroonian medicinal plants against Onchocerca gutturosa. Natural Product Research, 20(4), 391-397. doi:10.1080/14786410600661377. [NMR136]

Schliemann, W., Schneider, B., Wray, V., Schmidt, E., Nimtz, M., Porzel, A., Böhm, H. (2006). Flavonols and an indole alkaloid skeleton bearing identical acylated glycosidic groups from yellow petals of Papaver nudicaule. Phytochemistry, 67(2), 191-201. doi:10.1016/j.phytochem.2005.11.002. [NMR131]

Vergara, F., Svatoš, A., Schneider, B., Reichelt, M., Gershenzon, J., Wittstock, U. (2006). Glycine conjugates in a lepidopteran insect herbivore - The metabolism of benzylglucosinolate in the cabbage white butterfly, Pieris rapae. Chembiochem, 7(12), 1982-1989. doi:10.1002/cbic.200600280. [GER369]

Vogelsang, K., Schneider, B., Petersen, M. (2006). Production of rosmarinic acid and a new rosmarinic acid 3 '-O-beta-D-glucoside in suspension cultures of the hornwort Anthoceros agrestis Paton. Planta, 223(2), 369-373. doi:10.1007/s00425-005-0089-8. [NMR102]

2005

Antonchik, A. P., Svatos, A., Schneider, B., Konstantinova, O. V., Zhabinskii, V. N., Khripach, V. A. (2005). 2,3-Epoxybrassinosteroids are intermediates in the biosynthesis of castasterone in seedlings of Secale cereale. Phytochemistry, 66(1), 65-72. doi:10.1016/j.phytochem.2004.11.008. [NMR087]

Bednarek, P., Schneider, B., Svatos, A., Oldham, N. J., Hahlbrock, K. (2005). Structural complexity, differential response to infection, and tissue specificity of indolic and phenylpropanoid secondary metabolism in Arabidopsis roots. Plant Physiology, 138(2), 1058-1070. doi:10.1104/pp.104.057794. [NMR089]

Cheng, Y., Schneider, B., Oberthür, C., Graf, H., Adler, S., Hamburger, M. (2005). Flavone C-glycosides from Isatis tinctoria leaves. Heterocycles, 65(7), 1655-1661. doi:10.3987/COM-05-10343. [NMR091]

Hölscher, D., Schneider, B. (2005). The biosynthesis of 8-phenylphenalenones from Eichhornia crassipes involves a putative aryl migration step. Phytochemistry, 66(1), 59-64. doi:10.1016/j.phytochem.2004.10.019. [NMR086]

Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Khripach, N. B., Antonchik, A. V., Antonchik, A. P., Schneider, B. (2005). Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids. Steroids, 70(8), 551-562. doi:10.1016/j.steroids.2005.02.014. [NMR088]

Kuzovkina, I. N., Schneider, B. (2005). Genetically transformed root cultures - generation, properties and application in plant sciences. Progress in Botany, 67, 275-314. doi:10.1007/3-540-27998-9_13. [NMR092]

Schneider, B., Paetz, C., Hölscher, D., Opitz, S. (2005). HPLC-NMR for tissue-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Magnetic Resonance in Chemistry, 43(9), 724-728. doi:10.1002/mrc.1634. [NMR090]

2004

Antonchik, A. P., Schneider, B., Zhabinskii, V. N., Khripach, V. A. (2004). Synthesis of [26,27-H-²H₆] brassinosteroids from 23,24-bisnorcholenic acid methyl ester. Steroids, 69(10), 617-628. doi:10.1016/j.steroids.2004.05.014. [NMR084]

Bednarek, P., Winter, J., Hamberger, B., Oldham, N. J., Schneider, B., Tan, J.-W., Hahlbrock, K. (2004). Induction of 3 '-O-beta-D-ribofuranosyl adenosine during compatible, but not during incompatible, interactions of Arabidopsis thaliana or Lycopersicon esculentum with Pseudomonas syringae pathovar tomato. Planta, 218(4), 668-672. doi:10.1007/s00425-003-1146-9. [NMR077]

Cheng, Y., Schneider, B., Riese, U., Schubert, B., Li, Z., Hamburger, M. (2004). Farinosones A-C, neurotrophic alkaloidal metabolites from the entomogenous deuteromycete Paecilomyces farinosus. Journal of Natural Products, 67(11), 1854-1858. doi:10.1021/np049761w. [NMR085]

Kuzovkina, I. N., Al'terman, I., Schneider, B. (2004). Specific accumulation and revised structures of acridone alkaloid glucosides in the tips of transformed roots of Ruta graveolens. Phytochemistry, 65(8), 1095-1100. doi:10.1016/j.phytochem.2004.03.003. [NMR081]

Nookandeh, A., Frank, N., Steiner, F., Ellinger, R., Schneider, B., Gerhauser, C., Becker, H. (2004). Xanthohumol metabolites in faeces of rats. Phytochemistry, 65(5), 561-570. doi:10.1016/j.phytochem.2003.11.016. [NMR078]

Oberthur, C., Schneider, B., Graf, H., Hamburger, M. (2004). The elusive indigo precursors in woad (Isatis tinctoria L.) - Identification of the major indigo precursor, isatan A, and a structure revision of isatan B. Chemistry and Biodiversity, 1(1), 174-182. doi:10.1002/cbdv.200490009. [NMR082]

Otálvaro, F., Quinones, W., Echeverri, F., Schneider, B. (2004). Synthesis of [phenyl-¹³C₆]lachnanthocarpone and other ¹³C-labelled phenylphenalenones. Journal of Labelled Compounds and Radiopharmaceuticals, 47, 147-159. doi:10.1002/jlcr.808. [NMR080]

Schneider, B. (2004). Nuclear magnetic resonance applications to low-molecular metabolites in plant sciences. Progress in Botany, 65(65), 301-322. doi:10.1007/978-3-642-18819-0_12. [NMR083]

Schüler, G., Mithöfer, A., Baldwin, I. T., Berger, S., Ebel, S., Santos, J. G., Herrmann, G., Hölscher, D., Kramell, R., Kutchan, T. M., Maucher, H., Schneider, B., Stenzel, I., Wasternack, C., Boland, W. (2004). Coronalon: a powerful tool in plant stress physiology. FEBS Letters, 563(1-3), 17-22. doi:10.1016/S0014-5793(04)00239-X. [BOL159]

Svatos, A., Antonchik, A. P., Schneider, B. (2004). Determination of brassinosteroids in the sub-femtomolar range using dansyl-3-aminophenylboronate derivatization and electrospray mass spectrometry. Rapid Communications in Mass Spectrometry, 18(7), 816-821. doi:10.1002/rcm.1413. [MS042]

Tan, J.-W., Bednarek, P., Liu, J., Schneider, B., Svatos, A., Hahlbrock, K. (2004). Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves. Phytochemistry, 65(6), 691-699. doi:10.1016/j.phytochem.2003.12.009. [NMR079]

2003

Antonchik, A. P., Schneider, B., Zhabinskii, V. N., Konstantinova, O. V., Khripach, V. A. (2003). Biosynthesis of 2,3-epoxybrassinosteroids in seedlings of Secale cereale. Phytochemistry, 63(7), 771-776. doi:10.1016/S0031-9422(03)00354-6. [NMR074]

Baranovsky, A., Schmitt, B., Fowler, D. J., Schneider, B. (2003). Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies. Synthetic Communications, 33(6), 1019-1045. doi:10.1081/SCC-120016367. [NMR075]

Eckermann, C., Schröder, G., Eckermann, S., Strack, D., Schmidt, E., Schneider, B., Schröder, J. (2003). Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins. Phytochemistry, 62(3), 271-286. doi:10.1016/s0031-9422(02)00554-x. [NMR068]

Hölscher, D., Williams, D. C., Wildung, M. R., Croteau, R. (2003). A cDNA clone for 3-carene synthase from Salvia stenophylla. Phytochemistry, 62, 1081-1086. doi:10.1016/s0031-9422(02)00674-x. [NMR067]

Opitz, S., Schneider, B. (2003). Oxidative biosynthesis of phenylbenzoisochromenones from phenylphenalenones. Phytochemistry, 62(3), 307-312. doi:10.1016/S0031-9422(02)00546-0. [NMR066]

Opitz, S., Schnitzler, J. P., Hause, B., Schneider, B. (2003). Histochemical analysis of phenylphenalenone-related compounds in Xiphidium caeruleum (Haemodoraceae). Planta, 216(5), 881-889. doi:10.1007/s00425-002-0941-z. [NMR070]

Schneider, B. (2003). Differentiation-dependent levels of benzofuran-type resveratrol dimers in root cultures of Anigozanthos preissii. Phytochemistry, 64(2), 459-462. doi:10.1016/s0031-9422(03)00193-6. [NMR073]

Schneider, B., Gershenzon, J., Graser, G., Hölscher, D., Schmitt, B. (2003). One-dimensional 13C NMR and HPLC-1H NMR techniques for observing carbon-13 and deuterium labelling in biosynthetic studies. Phytochemistry Reviews, 2, 31-43. doi:10.1023/B:PHYT.0000004196.73829.4e. [NMR076]

Scholl, Y., Schneider, B., Dräger, B. (2003). Biosynthesis of calystegines: N-15 NMR and kinetics of formation in root cultures of Calystegia sepium. Phytochemistry, 62(3), 325-332. doi:10.1016/s0031-9422(02)00544-7. [NMR145]

2002

Berlich, M., Menge, S., Bruns, I., Schmidt, J., Schneider, B., Krauss, G.-J. (2002). Coumarins give misleading absorbance with Ellman's reagent suggestive of thiol conjugates. Analyst, 127(3), 333-336. doi:10.1039/b110988j. [NMR063]

Khripach, V. A., Zhabinskii, V. N., Antonchik, A. P., Konstantinova, O. V., Schneider, B. (2002). Synthesis of hexadeuterated 23-dehydroxybrassinosteroids. Steroids, 67(13-14), 1101-1108. doi:10.1016/S0039-128X(02)00071-5. [NMR014]

Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Antonchik, A. P., Schneider, B. (2002). Synthesis of [26-² H₃]brassinosteroids. Steroids, 67(7), 587-595. doi:10.1016/S0039-128X(02)00004-1. [NMR061]

Khripach, V. A., Zhabinskii, V. N., Konstantinova, O. V., Khripach, N. B., Antonchik, A. P., Schneider, B. (2002). [3,3]-Claisen rearrangements in 24 alpha-methyl steroid synthesis - Application to campesterol, crinosterol, and delta(25)-crinosterol side chain construction. Steroids, 67(7), 597-603. doi:10.1016/S0039-128X(02)00007-7. [NMR060]

Opitz, S., Hölscher, D., Oldham, N. J., Bartram, S., Schneider, B. (2002). Phenylphenalenone-related compounds: chemotaxonomic markers of the Haemodoraceae from Xiphidium caeruleum. Journal of Natural Products, 65(8), 1122-1130. doi:10.1021/np020083s. [NMR054]

Opitz, S., Otalvaro, F., Echeverri, F., Quinones, W., Schneider, B. (2002). Isomeric oxabenzochrysenones from Musa acuminata and Wachendorfia thyrsiflora. Natural Product Letters, 16(5), 335-338. doi:10.1080/10575630290033079. [NMR048]

Opitz, S., Schneider, B. (2002). Organ-specific analysis of phenylphenalenone-related compounds in Xiphidium caeruleum. Phytochemistry, 61(7), 819-825. doi:10.1016/S0031-9422(02)00359-X. [NMR056]

Otálvaro, F., Echeverri, F., Quinones, W., Torres, F., Schneider, B. (2002). Correlation between phenylphenalenone phytoalexins and phytopathological properties in Musa and the role of a dihydrophenylphenalene triol. Molecules, 7(3), 331-340. doi:10.3390/70300331. [NMR062]

Otálvaro, F., Görls, H., Hölscher, D., Schmitt, B., Echeverri, F., Quinones, W., Schneider, B. (2002). Dimeric phenylphenalenones from Musa acuminata and various Haemodoraceae species. Crystal structure of anigorootin. Phytochemistry, 60(1), 61-66. doi:10.1016/s0031-9422(02)00066-3. [NMR059]

Reichelt, M., Brown, P. D., Schneider, B., Oldham, N. J., Stauber, E. J., Tokuhisa, J. G., Kliebenstein, D. J., Mitchell-Olds, T., Gershenzon, J. (2002). Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana. Phytochemistry, 59(6), 663-671. doi:10.1016/S0031-9422(02)00014-6. [MPI020]

2001

Blitzke, T., Baranovsky, A., Schneider, B. (2001). Synthesis and protein binding of (4-carboxybutyl)carbamoyl- substituted taxoids. Helvetica Chimica Acta, 84(7), 1989-1995. doi:10.1002/1522-2675(20010711)84:7<1989:AID-HLCA1989>3.0.CO;2-M. [NMR034]

Gräther, O., Schneider, B. (2001). The metabolic diversity of plant cell and tissue cultures. In Progress in Botany (pp. 266-304). Berlin: Springer-Verlag. [NMR032]

Hagemeier, J., Schneider, B., Oldham, N. J., Hahlbrock, K. (2001). Accumulation of soluble and wall-bound indolic metabolites in Arabidopsis thaliana leaves infected with virulent or avirulent Pseudomonas syringae pathovar tomato strains. Proceedings of the National Academy of Sciences of the United States of America, 98(2), 753-758. doi:10.1073/pnas.021551098. [MPI009]

Konstantinova, O. V., Antonchik, A. P., Oldham, N. J., Zhabinskii, V. N., Khripach, V. A., Schneider, B. (2001). Analysis of underivatized brassinosteroids by HPLC/APCI-MS. Occurrence of 3-epibrassinolide in Arabidopsis thaliana. Collection of Czechoslovak Chemical Communications, 66(12), 1729-1734. doi:10.1135/cccc20011729. [MPI021]

Schmitt, B., Schneider, B. (2001). Phenylpropanoid interconversion in Anigozanthos preissii observed by high-performance liquid chromatography-nuclear magnetic resonance spectroscopy. Phytochemical Analysis, 12(1), 43-47. doi:10.1002/1099-1565(200101/02)12:1<43:AID-PCA546>3.0.CO;2-Z. [NMR030]

Schmitt, B., Schneider, B. (2001). Use of stable isotope labelling in biosynthetic studies on phenylphenalenones. In U. Pleiss, R. Veges (Eds.), Synthesis and Applications of Isotopically Labelled Compounds: Proceedings of the Seventh International Symposium, Dresden, Germany, 18-22 June 2000 (pp. 640-643). Chichester: Wiley. [NMR033]

Schneider, B. (2001). Analogies in the conversion of natural and synthetic substrates in plants revealed by labelling studies. In U. Pleiss, R. Veges (Eds.), Synthesis and Applications of Isotopically Labelled Compounds: Proceedings of the Seventh International Symposium, Dresden, Germany, 18-22 June 2000 (pp. 597-599). Chichester: Wiley. [NMR035]

Schneider, B. (2001). Pathways and enzymes of brassinosteroid biosynthesis. In Progress in Botany (pp. 286-306). Berlin: Springer-Verlag. [NMR052]

Sicker, D., Schneider, B., Hennig, L., Knop, M., Schulz, M. (2001). Correction to: Glycoside carbamates from benzoxazolin-2(3H)-one detoxification in extracts and exudates of corn roots (2001: 58, 819-825). Phytochemistry, 58, 819-825. doi:10.1016/S0031-9422(01)00299-0. [NMR053]

Stündl, U., Schneider, B. (2001). 3 beta-Brassinosteroid dehydrogenase activity in Arabidopsis and tomato. Phytochemistry, 58(7), 989-994. doi:10.1016/s0031-9422(01)00387-9. [NMR064]

2000

Graser, G., Schneider, B., Oldham, N. J., Gershenzon, J. (2000). The methionine chain elongation pathway in the biosynthesis of glucosinolates in Eruca sativa (Brassicaceae). Archives of Biochemistry and Biophysics, 378(2), 411-419. doi:10.1006/abbi.2000.1812. [MPI008]

Hölscher, D., Schneider, B. (2000). Phenalenones from Strelitzia reginae. Journal of Natural Products, 63(7), 1027-1028. doi:10.1021/np000035c. [NMR058]

Schmitt, B., Hölscher, D., Schneider, B. (2000). Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii. Phytochemistry, 53(3), 331-337. doi:10.1016/s0031-9422(99)00544-0. [NMR031]

Schneider, B. (2000). Natural products: Liquid chromatography - Nuclear Magnetic Resonance. in i. D. Wilson, T. R. Adlard, M. Cooke, C. F. Poole (Eds.), Encyclopedia of Separation Science (pp. 3434-3445). London: Academic Press. [NMR057]

1999

Adam, G., Schmidt, J., Schneider, B. (1999). Brassinosteroids. Progress in the Chemistry of Organic Natural Products, 78, 1-46. [NMR050]

Adam, G., Schneider, B. (1999). Uptake, transport and metabolism. In A. Sakurai, T. Yokota, S. D. Clouse (Eds.), Brassinosteroids: Steroidal Plant Hormones (pp. 113-136). Tokyo: Springer. [NMR001]

Fowler, D. J., Hamilton, J. T. G., Humphrey, A. J., O'Hagan, D. (1999). Plant terpene biosynthesis. The biosynthesis of linalyl acetate in Mentha citrata. Tetrahedron Letters, 40(19), 3803-3806. doi:10.1016/S0040-4039(99)00532-8. [NMR071]

Hartung, C., Illgen, K., Sieler, J., Schneider, B., Schulze, B. (1999). Synthesis of stable cyclic sulfinamides with a hydroperoxy function by oxidation of isothiazolium salts. Helvetica Chimica Acta, 82(5), 685-695. doi:10.1002/(SICI)1522-2675(19990505)82:5<685:AID-HLCA685>3.0.CO;2-4. [NMR006]

Hölscher, D., Schneider, B. (1999). HPLC-NMR analysis of phenylphenalenones and a stilbene from Anigozanthos flavidus. Phytochemistry, 50(1), 155-161. doi:10.1016/S0031-9422(98)00495-6. [NMR004]

Kolbe, A., Krauss, G., Schneider, B. (1999). Ornithopus sativus Brot. (Serradella): in vitro culture, phytochemical studies, and biotransformation. In Y. P. S. Bajaj (Ed.), Medicinal and Aromatic Plants XI. Biotechnology in Agriculture and Forestry (pp. 310-323). Berlin, Heidelberg: Springer. [NMR007]

Kolbe, A., Krauss, G., Schneider, B. (1999). Ornithopus sativus Brot. (Serradella): in vitro culture, phytochemical studies, and biotransformation. In Y. P. S. Bajaj (Ed.), Medicinal and aromatic plants XI (pp. 310-323). Berlin: Springer. [NMR047]

Mantrova, O. V., Dunaeva, M. V., Kuzovkina, I. N., Schneider, B., Muller-Uri, F. (1999). Effect of methyl jasmonate on anthraquinone biosynthesis in transformed madder roots. Russian Journal of Plant Physiology, 46(2), 248-251. [NMR029]

Röhl, I., Schneider, B., Schmidt, B., Zeeck, E. (1999). L-Ovothiol A: The egg release pheromone of the marine polychaete Platynereis dumerilii: Annelida: Polychaeta. Zeitschrift für Naturforschung, C: Journal of Biosciences, 54(12), 1145-1147. doi:10.1515/znc-1999-1222. [NMR069]

Schmitt, B., Schneider, B. (1999). Dihydrocinnamic acids are involved in the biosynthesis of phenylphenalenones in Anigozanthos preissii. Phytochemistry, 52(2), 45-53. doi:10.1016/S0031-9422(99)00116-8. [NMR002]

Schneider, B. (1999). Brassinosteroid metabolism. Chemicke Listy, 93(1), 12-14. [NMR016]

Schupp, P., Eder, C., Proksch, P., Wray, V., Schneider, B., Herderich, M., Paul, V. (1999). Staurosporine derivatives from the ascidian Eudistoma toealensis and its predatory flatworm Pseudoceros sp. Journal of Natural Products, 62(7), 959-962. doi:10.1021/np980527d. [NMR011]

Winter, J., Schneider, B., Meyenburg, S., Strack, D., Adam, G. (1999). Monitoring brassinosteroid biosynthetic enzymes by fluorescent tagging and HPLC analysis of their substrates and products. Phytochemistry, 51(2), 237-242. doi:10.1016/S0031-9422(98)00760-2. [NMR003]

Zhao, Y., Nookandeh, A., Schneider, B., Sun, X. F., Schmitt, B., Stöckigt, J. (1999). Lignans from Torreya jackii identified by stopped-flow high- performance liquid chromatography nuclear magnetic resonance spectroscopy. Journal of Chromatography A, 837(1-2), 83-91. doi:10.1016/S0021-9673(99)00050-3. [NMR005]

1998

Hölscher, D., Schneider, B. (1998). Phenylphenalenones from Ensete ventricosum. Phytochemistry, 49(7), 2155-2157. doi:10.1016/S0031-9422(98)00423-3. [NMR008]

Kolbe, A., Schneider, B., Porzel, A., Adam, G. (1998). Metabolic inversion of the 3-hydroxy function of brassinosteroids. Phytochemistry, 48(3), 467-470. doi:10.1016/S0031-9422(98)00037-5. [NMR009]

Kolbe, A., Schneider, B., Voigt, B., Adam, G. (1998). Labelling of biogenetic brassinosteroid precursors. Journal of Labelled Compounds and Radiopharmaceuticals, 41(2), 131-137. doi:10.1002/(SICI)1099-1344(199802)41:2<131:AID-JLCR59>3.0.CO;2-F. [NMR026]

Krause, U., Schneider, B. (1998). Investigations on the phenylpropane biosynthesis in in vitro cultures of Zingiberaceae spp. In P. Schreier, M. Herderich, H.-U. Humpf, W. Schwab (Eds.), Natural Product Analysis (pp. 393-394). Braunschweig/Wiesbaden: Vieweg. [NMR045]

Maier, W., Schneider, B., Strack, D. (1998). Biosynthesis of sesquiterpenoid cyclohexenone derivatives in mycorrhizal barley roots proceeds via the glyceraldehyde 3- phosphate/pyruvate pathway. Tetrahedron Letters, 39(7), 521-524. doi:10.1016/S0040-4039(97)10673-6. [NMR027]

Opitz, S., Koehler, G., Mabelis, A. (1998). Local movement of the grasshopper Chorthippus parallelus (Zett.). In M. J. Sommeijer, P. J. Francke (Eds.), Proceedings of the Section Experimental and Applied Entomology of the Netherlands Entomological Society (N.E.V.) (pp. 53-58). Netherlands Entomological Society, Plantage Middenlaan 64, 1018 DH Amsterdam 414, Netherlands. [GER073]

Opitz, S., Köhler, G., Mabelis, A. (1998). Grasshopper movement in a Dutch heathland - Chorthippus parallelus (Zett.). Proceedings of the Section Experimental and Applied Entomology of the Netherlands Entomological Society, 9, 53-58. [GER082]

Porzel, A., Hai, T., Kolbe, A., Schneider, B., Adam, G. (1998). Structure elucidation of brassinosteroid metabolites by NMR spectroscopy. In P. Schreier (Ed.), Natural Product Analysis (pp. 135-136). Braunschweig/Wiesbaden: Vieweg. [NMR046]

Schmitt, B., Schneider, B. (1998). NMR-Spectroscopic investigations on the dynamics of phenylpropane biosynthetic pathways in Anigozanthos preissii. In P. Schreier (Ed.), Natural Product Analysis (pp. 127-128). Braunschweig/Wiesbaden: Vieweg. [NMR044]

Schneider, B., Hölscher, D., Kolbe, A., Blitzke, T. (1998). HPLC-NMR in phytochemical analysis. In P. Schreier (Ed.), Natural Product Analysis (pp. 137-142). Braunschweig/Wiesbaden: Vieweg. [NMR043]

Schneider, B., Zhao, Y., Blitzke, T., Schmitt, B., Nookandeh, A., Sun, X. F., Stockigt, J. (1998). Taxane analysis by high performance liquid chromatography nuclear magnetic resonance spectroscopy of Taxus species. Phytochemical Analysis, 9(5), 237-244. doi:10.1002/(SICI)1099-1565(199809/10)9:5<237:AID-PCA411>3.0.CO;2-U. [NMR010]

Wieland, I., Kluge, M., Schneider, B., Schmidt, J., Sicker, D., Schulz, M. (1998). 3-beta-D-glucopyranosyl-benzoxazolin-2(3H)-one—A detoxification product of benzoxazolin-2(3H)-one in oat roots. Phytochemistry, 49(3), 719-722. doi:10.1016/S0031-9422(97)91012-8. [NMR028]

1997

Hölscher, D., Schneider, B. (1997). Phenylphenalenones from root cultures of Anigozanthos preissii. Phytochemistry, 45(1), 87-91. doi:10.1016/S0031-9422(96)00679-6. [NMR023]

Kluge, M., Schneider, B., Sicker, D. (1997). Diastereoselective synthesis of the benzoxazinone acetal glucoside ent-GDIMBOA: the first enantiomer of a natural acetal glucoside. Carbohydrate Research, 298(3), 147-152. doi:10.1016/S0008-6215(96)00303-5. [NMR022]

Kolbe, A., Porzel, A., Schneider, B., Adam, G. (1997). Diglycosidic metabolites of 24-epi-teasterone in cell suspension cultures of Lycopersicon esculentum L. Phytochemistry, 46(6), 1019-1022. doi:10.1016/S0031-9422(97)00390-7. [NMR025]

Schneider, B. (1997). In-vivo nuclear magnetic resonance spectroscopy of low-molecular-weight compounds in plant cells. Planta, 203(1), 1-8. doi:10.1007/s00050158. [NMR036]

Schneider, B., Kolbe, A., Winter, J., Porzel, A., Schmidt, J., Strack, D., Adam, G. (1997). Pathways and enzymology of brassinosteroid metabolism. In Proceedings of the Plant Growth Regulator Society of America, 24. Annual Meeting. [NMR042]

Winter, J., Schneider, B., Strack, D., Adam, G. (1997). Role of a cytochrome P450-dependent monooxygenase in the hydroxylation of 24-epi-brassinolide. Phytochemistry, 45(2), 233-237. doi:10.1016/S0031-9422(96)00827-8. [NMR024]

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