Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 1993; 1993(6): 391-392
DOI: 10.1055/s-1993-22465
DOI: 10.1055/s-1993-22465
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Synthesis of (±)-9ßH-Isopimara-7,15-dien-17-ol: A Naturally Occuring Diterpene with 9,10-syn Stereochemistry
Further Information
Publication History
Publication Date:
19 March 2002 (online)
A synthesis of the recently isolated 9ßH-isopimara-7,15-dien-17-ol starting from bicyclic 9ßH-drim-8(12)-en-11-al is reported. The third ring is closed by an intramolecular carbonyl ene reaction and the substituents at C-13 are introduced by a [2.3]-sigmatropic Wittig-Still rearrangement.