A catalytic aldol reaction between ketene silyl acetals and aldehydes promoted by lithium amide under non-acidic conditions

被引：52

作者：

Fujisawa, H ^{[1
]}

Mukaiyama, T ^{[1
]}

机构：

[1] Sci Univ Tokyo, Fac Sci, Dept Appl Chem, Shinjuku Ku, Tokyo 1628601, Japan

来源：

CHEMISTRY LETTERS | 2002年 / 02期

关键词：

D O I：

10.1246/cl.2002.182

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A catalytic aldol reaction between trimethylsilyl enol ethers and aldehydes by using lithium diphenylamide, a Lewis base catalyst, in DMF or pyridine solvent proceeded smoothly to afford the corresponding aldols under mild conditions.

引用

页码：182 / 183

页数：2

共 16 条

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[16] ORGANOMETALLIC HIGH-PRESSURE REACTION .2. ALDOL REACTION OF SILYL ENOL ETHERS WITH ALDEHYDES UNDER NEUTRAL CONDITIONS
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