Unified approach to prenylated indole alkaloids: total syntheses of (−)-17-hydroxy-citrinalin B, (+)-stephacidin A, and (+)-notoamide I-Reference-Cited by-同舟云学术

Unified approach to prenylated indole alkaloids: total syntheses of (−)-17-hydroxy-citrinalin B, (+)-stephacidin A, and (+)-notoamide I

Published:2015 Issue:8 Volume:6 Page:5048-5052
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Mercado-Marin Eduardo V.¹²³⁴,Sarpong Richmond¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of California–Berkeley

3. Berkeley

4. USA

Abstract

The first strategy that provides reverse-prenylated indole alkaloids that bear a characteristic bicyclo[2.2.2]diazaoctane as well as those that lack this structural motif is reported.

Funder

National Institutes of Health

NSF

ACS

UC Berkeley

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/SC/C5SC01977J

Reference45 articles.

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