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

Wesley J. Moran, Arantxa Rodríguez

Research output: Contribution to journalArticle

4 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 languageEnglish
Pages (from-to)33-35
Number of pages3
JournalRSC Advances
Volume1
Issue number1
Early online date18 Jul 2011
DOIs
Publication statusPublished - 7 Aug 2011

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Phenol
Phenols
Derivatives
illioliganone B
illioliganone C

Cite this

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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. / Moran, Wesley J.; Rodríguez, Arantxa.

In: RSC Advances, Vol. 1, No. 1, 07.08.2011, p. 33-35.

Research output: Contribution to journalArticle

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