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
收藏
页码：8303 / 8308
页数：6
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