Enantiodivergent synthesis of both antipodes of hydroxy-exo-brevicomin from L-(+)-tartaric acid

被引：19

作者：

Prasad, Kavirayani R. ^{[1
]}

Anbarasan, Pazhamalai ^{[1
]}

机构：

[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India

来源：

TETRAHEDRON | 2006年 / 62卷 / 35期

关键词：

stereoselective reduction; L-(+)-tartaric acid; hydroxy-exo-brevicomin; 6,8-dioxabicyclo[3.2.1]octane;

D O I：

10.1016/j.tet.2006.06.053

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An enantiodivergent approach to both antipodes of hydroxy-exo-brevicomin was achieved from a common chiral precursor L-(+)-tartaric acid. The strategy utilizes the elaboration of a keto-Weinreb amide and successive stereoselective reductions. (c) 2006 Elsevier Ltd. All rights reserved.

引用

页码：8303 / 8308

页数：6

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