BIOGENETIC-TYPE SYNTHESIS OF PENICILLIN-CEPHALOSPORIN ANTIBIOTICS .1. STEREOCONTROLLED SYNTHESIS OF PENAM-RING AND CEPHEM-RING SYSTEMS FROM AN ACYCLIC TRIPEPTIDE EQUIVALENT

被引：65

作者：

NAKATSUKA, S ^{[1
]}

TANINO, H ^{[1
]}

KISHI, Y ^{[1
]}

机构：

[1] HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1975年 / 97卷 / 17期

关键词：

D O I：

10.1021/ja00850a042

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：5008 / 5010

页数：3

共 32 条

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[7] STRUCTURAL STUDIES ON PENICILLIN DERIVATIVES .8. POSSIBLE MODEL BIOSYNTHETIC ROUTE TO PENAMS AND CEPHEMS
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (03) : 1018 - &
[8] DEMIAN AL, 1963, T NY ACAD SCI, V25, P731
[9] EDWARDS JA, 1974, TETRAHEDRON LETT, P2031
[10] TOTAL SYNTHESIS OF BETA-LACTAM ANTIBIOTICS .4. EPIMERIZATION OF 6(7)-AMINOPENICILLINS AND 6(7)-CEPHALOSPORINS FROM ALPHA TO BETA
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