A total and practical synthesis of ergot alkaloid, (.+-.)-aurantioclavine.
Open Access
- 1 January 1985
- journal article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 33 (5) , 2162-2163
- https://doi.org/10.1248/cpb.33.2162
Abstract
The first synthesis of (±)-aurantioclavine by a convenient and practical five-step synthetic method, involving a new intra-molecular cyclization of nitro-olefin, is achieved starting from 3-formylindole with a 31% overall yield without using any protective groupsKeywords
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