THE ASYMMETRIC-SYNTHESIS OF BETA-LACTAM ANTIBIOTICS .1. APPLICATION OF CHIRAL OXAZOLIDONES IN THE STAUDINGER REACTION

被引：217

作者：

EVANS, DA

SJOGREN, EB

机构：

来源：

TETRAHEDRON LETTERS | 1985年 / 26卷 / 32期

关键词：

D O I：

10.1016/S0040-4039(00)89250-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3783 / 3786

页数：4

共 10 条

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[2]

EVANS DA, 1985, TETRAHEDRON LETT

[3]

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[6] SYNTHETIC STUDIES ON OPTICALLY-ACTIVE BETA-LACTAMS - ASYMMETRIC-SYNTHESIS OF BETA-LACTAMS BY THE CYCLOCONDENSATION UTILIZING CHIRAL HETEROCYCLIC-COMPOUNDS DERIVED FROM L-(+)-TARTARIC ACID AND (S)-GLUTAMIC ACID [J].

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HANAKI, A .

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[7] STEREOSPECIFIC CONSTRUCTIONS OF CHIRAL BETA-LACTAMS [J].

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[8] THE ASYMMETRIC DIELS-ALDER REACTIONS OF ALPHA, BETA-UNSATURATED CARBOXYLIC AMIDES DERIVED FROM (-)-PHENYLGLYCINOL AND THE ASYMMETRIC TOTAL SYNTHESIS OF (+)-FARNESIFEROL-C [J].

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[9] IMPROVED CHIRAL DERIVATIZING AGENTS FOR THE CHROMATOGRAPHIC RESOLUTION OF RACEMIC PRIMARY AMINES [J].

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[10]

WEI CC, 1983, 23RD INT C ANT AG CH

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