FROM AZIRIDINES TO CARBAPENEMS VIA A NOVEL BETA-LACTAM RING-CLOSURE - AN ENANTIOSELECTIVE SYNTHESIS OF (+)-PS-5

被引：68

作者：

TANNER, D

SOMFAI, P

机构：

来源：

TETRAHEDRON | 1988年 / 44卷 / 02期

关键词：

D O I：

10.1016/S0040-4020(01)85849-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

收藏

页码：619 / 624

页数：6

相关论文

共 13 条

[11] A MILD AND EFFICIENT METHOD FOR THE PREPARATION OF N-TOSYL AMIDES AND LACTAMS [J].

TANNER, D ;

SOMFAI, P .

TETRAHEDRON, 1988, 44 (02) :613-618

[12] AN AZIRIDINE ROUTE TO CHIRAL BETA-LACTAMS A NOVEL ENTRY TO (+)-THIENAMYCIN [J].

TANNER, D ;

SOMFAI, P .

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[13] A CIS HYDROXYAMINATION EQUIVALENT - APPLICATION TO THE SYNTHESIS OF (-)-ACOSAMINE [J].

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (12) :3792-3794