THE SYNTHESIS AND REACTIONS OF A MONOCYCLIC BETA-LACTAM TRIPEPTIDE, 1-[(1R)-CARBOXY-2-METHYLPROPYL]-(3R)-[(5S)-5-AMINO-5-CARBOXYPENTANAMIDO]-(4R)-MERCAPTOAZETIDIN-2-ONE, A PUTATIVE INTERMEDIATE IN PENICILLIN BIOSYNTHESIS

被引：15

作者：

BALDWIN, JE ^{[1
]}

ABRAHAM, EP ^{[1
]}

ADLINGTON, RM ^{[1
]}

CRIMMIN, MJ ^{[1
]}

FIELD, LD ^{[1
]}

JAYATILAKE, GS ^{[1
]}

WHITE, RL ^{[1
]}

USHER, JJ ^{[1
]}

机构：

[1] UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,OXFORD OX1 3RE,ENGLAND

来源：

TETRAHEDRON | 1984年 / 40卷 / 10期

关键词：

D O I：

10.1016/S0040-4020(01)91148-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1907 / 1918

页数：12

共 19 条

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[2]

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[7]

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[9] UNUSUAL STEREOSPECIFICITY IN THE HYDROGENATION OF AN ISOPROPENYL FUNCTION WITH WILKINSONS CATALYST - A ROUTE TO CHIRAL METHYL VALINE [J].

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[10] CONVERSION OF ISOPENICILLIN-N INTO PENICILLIN-N IN CELL-FREE-EXTRACTS OF CEPHALOSPORIUM-ACREMONIUM [J].

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BIOCHEMICAL JOURNAL, 1981, 194 (02) :645-647

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