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Vinceten, ein Benzopyrroloisochinolin-Alkaloid aus Cynanchum vincetoxicum (L.) Pers. (Asclepiadaceae)
Budzikiewicz, H., Faber, L., Herrmann, E.-G., Perrollaz, F. F., Schlunegger, U.P . and Wiegrebe, Wolfgang (1979) Vinceten, ein Benzopyrroloisochinolin-Alkaloid aus Cynanchum vincetoxicum (L.) Pers. (Asclepiadaceae). Justus Liebigs Annalen der Chemie, pp. 1212-1231.Date of publication of this fulltext: 22 Jun 2010 09:52
Article
DOI to cite this document: 10.5283/epub.15501
Abstract
Cynanchum vincetoxicum (L.) Pers. enthält Spuren eines Alkaloids C22H27NO3, dessen Struktur als 6-(3-Hydroxy-os-l-butenyl)-2,3-dimethoxy-7,9,10,11,11 a, 12-hexahydrobenzo[/]pyrrolo[ 1,2-b]- isochinolin (2) geklärt und durch Synthese des rac-Dihydrodesoxy-Derivates 18 gesichert wurde. Cynanchum vincetoxicum contains traces of an alkaloid C22H27NO3, whose structure has been shown to be ...
Cynanchum vincetoxicum (L.) Pers. enthält Spuren eines Alkaloids C22H27NO3, dessen Struktur
als 6-(3-Hydroxy-os-l-butenyl)-2,3-dimethoxy-7,9,10,11,11 a, 12-hexahydrobenzo[/]pyrrolo[ 1,2-b]-
isochinolin (2) geklärt und durch Synthese des rac-Dihydrodesoxy-Derivates 18 gesichert wurde.
Cynanchum vincetoxicum contains traces of an alkaloid C22H27NO3, whose structure has been
shown to be 6-(3-hydroxy-c/5-l-butenyl)-2,3-dimethoxy-7,9,10,ll,lla,12-hexahydrobenzo[/lpyrrolo[
l,2-Z?]isoquinoline (2) and has been confirmed by synthesis of the rac-dihydrodesoxyderivative
18.
Involved Institutions
Details
| Item type | Article |
| Journal or Publication Title | Justus Liebigs Annalen der Chemie |
| Page Range: | pp. 1212-1231 |
|---|---|
| Date | 1979 |
| Institutions | Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe |
| Dewey Decimal Classification | 500 Science > 540 Chemistry & allied sciences |
| Status | Published |
| Refereed | Yes, this version has been refereed |
| Created at the University of Regensburg | Unknown |
| URN of the UB Regensburg | urn:nbn:de:bvb:355-epub-155018 |
| Item ID | 15501 |
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