DIASTEREOSELECTIVE REDUCTION OF ALPHA-KETO ESTERS DERIVED FROM FUNCTIONALIZED CHOLIC-ACID

被引：50

作者：

MAITRA, U

PACKIARAJAN, M

机构：

[1] Department of Organic Chemistry, Indian Institute of Science, Bangalore

来源：

TETRAHEDRON-ASYMMETRY | 1994年 / 5卷 / 07期

关键词：

D O I：

10.1016/0957-4166(94)80149-5

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The reduction of phenylglyoxalate 2a and pyruvate 2b with LiBH4 in THF at -80 degrees C yield the corresponding alpha-hydroxy esters with ca. 70% diastereoselectivity.

引用

页码：1171 / 1174

页数：4

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