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.
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页码：1455 / 1458
页数：4
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