A new synthesis of (.+-.)-vindorosine.
- 1 January 1984
- journal article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 32 (6) , 2477-2479
- https://doi.org/10.1248/cpb.32.2477
Abstract
The pentacyclic compound (15) was stereoselectively synthesized in the racemic form using indole and acetylpyridine as starting materials according to the synthetic route shown in Chart 2. This constitutes a new formal synthesis of (±)-vindorosine (16).Keywords
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