Total Synthesis of (±)-Herbindole A, (±)-Herbindole B, and (±)-cis-Trikentrin A
Author:
Affiliation:
1. Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo062350v
Reference24 articles.
1. Polyalkylated cyclopentindoles: Cytotoxic fish antifeedants from a sponge, Axinella sp.
2. Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 11. Total Synthesis of (6R,8S)-Herbindole A, (6R,8S)-Herbindole B, (6R,8S)-Herbindole C, (6R,8S)-cis-Trikentrin A, (6R,8S)-cis-Trikentrin B, (6R,8R)-trans-Trikentrin B, and (6R,8R)-iso-trans-Trikentrin B. Determination of the Absolute Structures of Natural Herbindoles and Trikentrins.
3. Preparation of Alkyl-Substituted Indoles in the Benzene Portion. Part 10. Synthesis of 4- and/or 5-Alkylated 1,6,7,8-Tetrahydrocyclopent(g)indoles, Model Compounds for Herbindole and Trikentrin Syntheses.
4. The trikentrins : novel indoles from the sponge
5. The synthesis of (±) cis-trikentrin a
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