DIASTEREOMERIC 7-UREIDOACETYL CEPHALOSPORINS .1. SUPERIORITY OF 7-ALPHA-H-L-ISOMERS OVER D-ISOMERS

被引：6

作者：

BREUER, H ^{[1
]}

TREUNER, UD ^{[1
]}

SCHNEIDER, HJ ^{[1
]}

YOUNG, MG ^{[1
]}

BASCH, HI ^{[1
]}

机构：

[1] SQUIBB INST MED RES,PRINCETON,NJ 08540

来源：

JOURNAL OF ANTIBIOTICS | 1978年 / 31卷 / 06期

关键词：

D O I：

10.7164/antibiotics.31.546

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

引用

页码：546 / 560

页数：15

共 20 条

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[5] DIASTEREOMERIC 7-UREIDOACETYL CEPHALOSPORINS .3. CONTRIBUTION OF D-ISOMERS AND L-ISOMERS TO GROWTH INHIBITING ACTIVITIES OF 7-ALPHA-H AND 7-ALPHA-OCH3 DERIVATIVES FOR GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA [J].

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[10] SEMISYNTHETIC CEPHALOSPORINS - SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF "7-MANDELAMIDO-3-CEPHEM-4-CARBOXYLIC ACIDS [J].

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