Application of a Palladium‐Catalyzed C−H Functionalization/Indolization Method to Syntheses of cis ‐Trikentrin A and Herbindole B-Reference-Cited by-同舟云学术

Application of a Palladium‐Catalyzed C−H Functionalization/Indolization Method to Syntheses of cis ‐Trikentrin A and Herbindole B

Published:2016-08-29 Issue:39 Volume:128 Page:12003-12007
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Leal Raul A.¹,Bischof Caroline¹,Lee Youjin V.¹,Sawano Shota¹,McAtee Christopher C.¹,Latimer Luke N.²,Russ Zachary N.²,Dueber John E.²,Yu Jin‐Quan³,Sarpong Richmond¹^ORCID

Affiliation:

1. Department of Chemistry University of California, Berkeley Berkeley CA 94720 USA

2. Department of Bioengineering University of California, Berkeley Berkeley CA 94720 USA

3. Department of Chemistry The Scripps Research Institute La Jolla CA 92037 USA

Funder

US National Science Foundation (NSF)

US NSF

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201605475

Reference62 articles.

1. Polyalkylated cyclopentindoles: Cytotoxic fish antifeedants from a sponge, Axinella sp.

2. The trikentrins : novel indoles from the sponge

3. Total syntheses of trikentrins and of herbindoles

4. For syntheses of herbindole B see:

5. Total synthesis of (+)-Herbindole A, (+)-herbindole B, and (+)-herbindole C. Determination of the absolute configuration of the natural herbindoles

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