BIOGENETIC-TYPE SYNTHESIS OF PENICILLIN-CEPHALOSPORIN ANTIBIOTICS .2. OXIDATIVE CYCLIZATION ROUTE TO BETA-LACTAM THIAZOLINE DERIVATIVES

被引：36

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/ja00850a043

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：5010 / 5012

页数：3

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[1] BIOSYNTHESIS OF PENICILLIN .6. STUDY OF THE MECHANISM OF THE FORMATION OF THE THIAZOLIDINE-BETA-LACTAM RINGS, USING TRITIUM-LABELLED CYSTINE
ARNSTEIN, HRV
CRAWHALL, JC
[J]. BIOCHEMICAL JOURNAL, 1957, 67 : 180 - 187
[2] STRUCTURAL STUDIES ON PENICILLIN DERIVATIVES .8. POSSIBLE MODEL BIOSYNTHETIC ROUTE TO PENAMS AND CEPHEMS
COOPER, RDG
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (03) : 1018 - &
[3] BIOGENETIC-TYPE SYNTHESIS OF PENICILLIN-CEPHALOSPORIN ANTIBIOTICS .1. STEREOCONTROLLED SYNTHESIS OF PENAM-RING AND CEPHEM-RING SYSTEMS FROM AN ACYCLIC TRIPEPTIDE EQUIVALENT
NAKATSUKA, S
TANINO, H
KISHI, Y
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (17) : 5008 - 5010
[4] NAKATSUKA S, IN PRESS