Lewis base-catalyzed Mannich-type reaction between aldimine and trimethylsilyl enolate

被引：40

作者：

Fujisawa, H ^{[1
]}

Takahashi, E ^{[1
]}

Nakagawa, T ^{[1
]}

Mukaiyama, T ^{[1
]}

机构：

[1] Kitasato Univ, Kitasato Inst Life Sci, Minato Ku, Tokyo 1088641, Japan

来源：

CHEMISTRY LETTERS | 2003年 / 32卷 / 11期

关键词：

D O I：

10.1246/cl.2003.1036

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Lithium benzamide- or potassium phthalimide-catalyzed Mannich-type reaction between trimethylsilyl enolates and aldimines proceeded smoothly in a DMF solvent to afford the corresponding beta-amino esters in good to high yields.

引用

页码：1036 / 1037

页数：2

共 32 条

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