4.4 Article

First total synthesis of salinipyrone A using highly stereoselective vinylogous Mukaiyama aldol reaction

期刊

TETRAHEDRON
卷 68, 期 45, 页码 9289-9292

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2012.08.035

关键词

Aldol reaction; Wittig olifination; Cyclization; Salinipyrones; Pacificanones

资金

  1. CSIR-UGC, New Delhi, India

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A synthetic approach for the total synthesis of salinipyrone A has been developed. Key steps involve the TiCl4-mediated vinylogous Mukaiyama aldol reaction (VMAR) of chiral ketene silyl N,O-acetal with propionaldyhyde, an aldol condensation, Witting olefination, and a cyclization. The synthesis proceeds in eight steps. (C) 2012 Elsevier Ltd. All rights reserved.

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