BORON-TRIFLUORIDE PROMOTED ALDOL REACTION OF SILYL KETENE ACETALS WITH THE INTERMEDIATE GENERATED BY THE DIBALH REDUCTION OF CARBOXYLIC-ACID ESTERS

被引：30

作者：

KIYOOKA, S

SHIROUCHI, M

机构：

[1] Department of Chemistry, Kochi University, Akebono-cho

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1992年 / 57卷 / 01期

关键词：

D O I：

10.1021/jo00027a001

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The intermediate generated by the DIBALH reduction of carboxylic acid esters undergoes a boron trifluoride promoted aldol reaction with silyl ketene acetals to afford the corresponding beta-hydroxy carboxylic acids esters in good yield.

引用

页码：1 / 2

页数：2

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