INTRAMOLECULAR MICHAEL ADDITION OF CHIRAL IMINES TO ENOATES - A NEW ASYMMETRIC CARBOCYCLIZATION REACTION

被引：26

作者：

DUMAS, F

DANGELO, J

机构：

[1] Unité de Chimie Organique Associée au CNRS, ESPCI, 75231 Paris Cedex 05

来源：

TETRAHEDRON-ASYMMETRY | 1990年 / 1卷 / 03期

关键词：

D O I：

10.1016/S0957-4166(00)82371-X

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Imines 6-8 have been cyclized into ketones 9-11 by using three methods of activation: heating, high pressure and Lewis acid (MgBr2). Low to excellent stereoselectivities were observed. © 1990.

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页码：167 / 170

页数：4

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