Enantioselective construction of the tricyclic core of curcusones A–D via a cross-electrophile coupling approach-Reference-Cited by-同舟云学术

Enantioselective construction of the tricyclic core of curcusones A–D via a cross-electrophile coupling approach

Published:2019 Issue:45 Volume:10 Page:10562-10565
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Wright Austin C.¹²³⁴⁵,Stoltz Brian M.¹²³⁴⁵^ORCID

Affiliation:

1. Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering

2. Division of Chemistry and Chemical Engineering

3. California Institute of Technology

4. Pasadena

5. USA

Abstract

Rapid assembly of the carbocyclic core of the curcusone family of natural products is achieved using reductive cross coupling and ring-closing metathesis disconnections.

Funder

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC04127C

Reference21 articles.

1. Isolation and structure determination of four novel diterpenes from jatropha curcus

2. Spirocurcasone, a Diterpenoid with a Novel Carbon Skeleton from Jatropha curcas

3. Cytotoxicity of naturally occurring rhamnofolane diterpenes from Jatropha curcas

4. L.—A theoretical derivation of the principle of induced alternate polarities

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