Issue 1, 2011

An oxidative Hosomi-Sakurai strategy toward the synthesis of illioliganones B and C

Abstract

The core structures of illioliganones B and C have been made by an oxidative Hosomi-Sakurai reaction of a phenol derivative. The use of a silyl protecting group is shown to be crucial for this reaction to proceed.

Graphical abstract: An oxidative Hosomi-Sakurai strategy toward the synthesis of illioliganones B and C

Supplementary files

Article information

Article type
Communication
Submitted
21 Apr 2011
Accepted
03 Jun 2011
First published
18 Jul 2011

RSC Adv., 2011,1, 33-35

An oxidative Hosomi-Sakurai strategy toward the synthesis of illioliganones B and C

W. J. Moran and A. Rodríguez, RSC Adv., 2011, 1, 33 DOI: 10.1039/C1RA00095K

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