Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kim, Messer"'
Autor:
Karl Peters, Doris Feineis, Gerhard Bringmann, Katja Maksimenka, Jörg Mühlbacher, Miriam Münchbach, Ralf God, Kim Messer, Eva-Maria Peters, Klaus-Peter Gulden
Publikováno v:
Tetrahedron. 60:8143-8151
Separation and stereochemical attribution of the two enantiomers of the neurotoxin 1-trichloromethyl-1,2,3,4-tetrahydro-β-carboline (TaClo) has been achieved by applying chromatography on a chiral phase HPLC column in hyphenation with circular dichr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de368ade22c3c56771002da21fc6bd27
https://doi.org/10.1016/j.tet.2004.06.093
https://doi.org/10.1016/j.tet.2004.06.093
Autor:
Matthias Reichert, Gábor Tóth, Matthias Breuning, Michaela Schraut, Robert-Michael Pfeifer, Kim Messer, Gerhard Bringmann
Publikováno v:
Zeitschrift für Naturforschung B. 59:100-105
The first X-ray structure analysis of authentic, not derivatized (racemic) trans-isoshinanolone, a wide-spread acetogenic tetralone, is described. In the crystal, two slightly different conformers are found, along with the corresponding enantiomers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37a116ac16df40b3f7d7e6652661b55c
https://doi.org/10.1515/znb-2004-0114
https://doi.org/10.1515/znb-2004-0114
Publikováno v:
Phytochemistry. 62:345-349
The isolation, structural elucidation, and antiprotozoal activities of habropetaline A, a novel naphthylisoquinoline alkaloid from Triphyophyllum peltatum , are described. This alkaloid had previously only been identified on line, by the LC–MS/MS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74966410bf9dc40232ff3bf6e6d748c0
https://doi.org/10.1016/s0031-9422(02)00547-2
https://doi.org/10.1016/s0031-9422(02)00547-2
Autor:
Peter Proksch, Victor Wray, Rainer Ebel, Gerhard Bringmann, Jörg Mühlbacher, Michael Dreyer, Kim Messer, Bambang W. Nugroho
Publikováno v:
Journal of Natural Products. 66:80-85
Two rocaglamide-related natural products, the previously known compound 6-demethoxy-10-hydroxy-11-methoxy-6,7-methylendioxyrocaglamide (3), and cyclorocaglamide (4), its 8b,10-anhydro analogue, have been isolated from the tropical plant Aglaia oligop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0db4b65a0143176fc1586b62f79926e7
https://doi.org/10.1021/np020291k
https://doi.org/10.1021/np020291k
Publikováno v:
Journal of Natural Products. 65:1096-1101
Four new naphthylisoquinoline alkaloids, ancistrocongolines A-D (4-7) were isolated from Ancistrocladus congolensis, along with the known compound korupensamine A (8). Structural elucidation was achieved by chemical, spectroscopic, and chiroptical me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c84adbb607cab86a7260495df8ea090
https://doi.org/10.1021/np010622d
https://doi.org/10.1021/np010622d
Autor:
Kim Messer, Reto Brun, Jörg Mühlbacher, Gerhard Bringmann, Adriaan M. Louis, Matthias Grüne, Kristina Wolf
Publikováno v:
Phytochemistry. 60:389-397
The isolation and structural elucidation of dioncophylline E, a novel naphthylisoquinoline alkaloid from the rare West African liana Dioncophyllum thollonii, is described. The alkaloid displays an unusual 7,3'-linkage between the naphthalene and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fbf970d6ce39e13fec862eee2d7be83
https://doi.org/10.1016/s0031-9422(02)00109-7
https://doi.org/10.1016/s0031-9422(02)00109-7
Autor:
Gerhard Bringmann, Kim Messer, Miriam Münchbach, Stefanie Diem, Wilfried Kuhn, Markus Herderich, Hans-Willi Clement, Christine Stichel-Gunkel, Doris Feineis
Publikováno v:
Journal of Chromatography B. 767:321-332
An improved sensitive assay for the determination of the dopaminergic and serotonergic neurotoxin 1-trichloromethyl-1,2,3,4-tetrahydro-β-carboline (TaClo) is presented, based upon on-line coupling of high-performance liquid chromatography with elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34ff3b72e0829152dbb63afe642b8a9b
https://doi.org/10.1016/s1570-0232(01)00589-x
https://doi.org/10.1016/s1570-0232(01)00589-x
Publikováno v:
Phytochemistry. 56:387-391
The absolute configuration of (+)-isoshinanolone, a wide-spread acetogenic metabolite from higher plants, has been determined by X-ray structure analysis of its new dibromide; accordingly, this natural tetralone is 3R,4R-configured, in agreement with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f2ab558b97628c38a6d123ac03dc09a
https://doi.org/10.1016/s0031-9422(00)00386-1
https://doi.org/10.1016/s0031-9422(00)00386-1
Publikováno v:
Tetrahedron. 56:5871-5875
The synthesis of jozipeltine A (5), the 6′-coupled constitutionally symmetric dimer of the highly antimalarial naphthylisoquinoline alkaloid dioncopeltine A (4), is described. After selective protection of two of the four OH- and NH-functionalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::490d278ec179b626947c90ebe2dce7a9
https://doi.org/10.1016/s0040-4020(00)00538-x
https://doi.org/10.1016/s0040-4020(00)00538-x
Publikováno v:
Synthesis. 2000:1843-1847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adf41e58ee1af38eb324c66d17296e22
https://doi.org/10.1055/s-2000-8236
https://doi.org/10.1055/s-2000-8236