4.4 Article

The stereoselective total synthesis of (+)-garvensintriol

期刊

TETRAHEDRON LETTERS
卷 51, 期 42, 页码 5529-5531

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.07.158

关键词

Sharpless kinetic resolution; Stereoselective epoxide opening; MacMillan alpha-hydroxylation; Horner-Wadsworth-Emmons reaction; Styryl lactones

资金

  1. UGC, New Delhi

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A simple and highly efficient stereoselective total synthesis of (+)-garvensintriol, isolated from the stem bark of Goniothalamas arvensis, is described using Sharpless kinetic resolution, MacMillan, alpha-hydroxylation, and Horner-Wadsworth-Emmons olefination as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.

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