DIASTEREO AND ENANTIOSELECTIVE ENTRY TO BETA-AMINO ESTERS BY HYDRIDE REDUCTION OF HOMOCHIRAL BETA-ENAMINO ESTERS

被引：40

作者：

CIMARELLI, C

PALMIERI, G

BARTOLI, G

机构：

[1] DIPARTIMENTO SCI CHIM,I-62032 CAMERINO,ITALY

[2] DIPARTIMENTO CHIM ORGAN A MANGINI,I-40136 BOLOGNA,ITALY

来源：

TETRAHEDRON-ASYMMETRY | 1994年 / 5卷 / 08期

关键词：

D O I：

10.1016/0957-4166(94)80111-8

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The reduction of homochiral beta-enamino esters 1 with sodium triacetoxyborohydride, which occurs with good diastereo- and enantioselectivity in the beta-amino esters 2, is described. This procedure allows a straightforward preparation of compounds with known biological activity.

引用

页码：1455 / 1458

页数：4

共 24 条

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