• search hit 4 of 93
Back to Result List

Zur Stereochemie der Bisaboloide aus Matricaria chamomilla L.

On the stereochemistry of the bisaboloids from matricaria chamomilla L.

  • The stereochemistry of the bisaboloids in chamomile-with the exception of bisabolol-oxide C-has been elucidated. The in-vitro-examination of the mutual convertibilities of some bisaboloids gave evidence for the stereochemical accordance of the common chiral centres of all the bisaboloids. The absolute configurations of the remaining third asymmetric carbon atoms in bisabololoxide A and B have been determined by NMR spectrometric studies in comparison with their unnatural semisynthetic epimers. All the stereogenic centres of the bisabololoxides A and B, of (-)-α-bisabolol and of bisabolonoxide A turn out to be S-configurated.

Download full text files

Export metadata

Additional Services

Share in Twitter Search Google Scholar
Metadaten
Author:Elmar FlaskampGND, Gerhard NonnenmacherGND, Gottfried ZimmermannGND, Otto Isaac
URN:urn:nbn:de:hebis:30:3-719511
DOI:https://doi.org/10.1515/znb-1981-0822
ISSN:1865-7117
ISSN:0932-0776
Parent Title (German):Zeitschrift für Naturforschung, B
Publisher:Verlag der Zeitschrift für Naturforschung
Place of publication:Tübingen
Document Type:Article
Language:German
Date of Publication (online):2014/06/02
Year of first Publication:1981
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2024/01/09
Tag:13C NMR Spectra; Bisaboloids; Matricaria chamomilla L; Shift-Reagents
Volume:36.1981
Issue:8
Page Number:8
First Page:1023
Last Page:1030
Institutes:Biochemie, Chemie und Pharmazie / Biochemie und Chemie
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung-Nicht kommerziell-Keine Bearbeitung 3.0