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

Wesley J. Moran; Arantxa Rodríguez

doi:10.1039/c1ra00095k

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

Wesley J. Moran, Arantxa Rodríguez

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

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.

Original language	English
Pages (from-to)	33-35
Number of pages	3
Journal	RSC Advances
Volume	1
Issue number	1
Early online date	18 Jul 2011
DOIs	https://doi.org/10.1039/c1ra00095k
Publication status	Published - 7 Aug 2011

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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.",

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

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