Diastereoselective protonation of enolates of chiral Schiff bases

被引：10

作者：

Tabcheh, M

Guibourdenche, C

Pappalardo, L

Roumestant, ML

Viallefont, P

机构：

[1] Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Proteines, F-34095 Montpellier 5, France

[2] Univ Montpellier 2, F-34095 Montpellier, France

来源：

TETRAHEDRON-ASYMMETRY | 1998年 / 9卷 / 09期

关键词：

D O I：

10.1016/S0957-4166(98)00133-5

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Diastereoselective protonation of potassium enolates of chiral Schiff bases prepared from racemic alpha-amino esters and 2-hydroxypinan-3-one afforded, after mild cleavage of the imine function, optically active alpha-amino esters. (C) 1998 Elsevier Science Ltd. All rights reserved.

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页码：1493 / 1495

页数：3

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