FUNCTIONALIZATION OF C6(7) OF PENICILLINS AND CEPHALOSPORINS - ONE-STEP STEREOSELECTIVE SYNTHESIS OF 7-ALPHA-METHOXYCEPHALOSPORIN C

被引：95

作者：

KOPPEL, GA ^{[1
]}

KOEHLER, RE ^{[1
]}

机构：

[1] ELI LILLY & CO,LILLY RES LABS,INDIANAPOLIS,IN 46206

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1973年 / 95卷 / 07期

关键词：

D O I：

10.1021/ja00788a072

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：2403 / 2404

页数：2

共 10 条

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[2] SUBSTITUTED PENICILLIN AND CEPHALOSPORIN DERIVATIVES .1. STEREOSPECIFIC INTRODUCTION OF C-6(7) METHOXY GROUP [J].

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[4] ELECTROPHILIC OPENING OF THIAZOLIDINE RING IN PENICILLINS [J].

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[5] BETA-LACTAM ANTIBIOTICS FROM STREPTOMYCES [J].

NAGARAJAN, R ;

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[6]

RATCLIFFE RW, 1972, TETRAHEDRON LETT, P2910

[7]

SPITZER WG, TO BE PUBLISHED

[8]

SPRY DO, 1972, TETRAHEDRON LETT, P3717

[9]

SPRY DO, TO BE PUBLISHED

[10]

STAPLEY EO, 1971, 11 INT C ANT AG CHEM, P8

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