SURPRISINGLY HIGH DIASTEREOSELECTION IN THE ALDOL REACTIONS OF SODIUM ENOLATES OF ALPHA-AMINO METHYL KETONES

被引：17

作者：

LAGU, BR ^{[1
]}

LIOTTA, DC ^{[1
]}

机构：

[1] EMORY UNIV,DEPT CHEM,ATLANTA,GA 30322

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 26期

关键词：

D O I：

10.1016/S0040-4039(00)60707-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Kinetic enolates of a number of alpha-(N,N-dibenzyl)amino methyl ketones were allowed to react with a variety of aldehydes. High diastereoselectivity was observed for sodium enolates compared to their lithium counterparts.

引用

页码：4485 / 4488

页数：4

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