A STEREOSELECTIVE ROUTE TO THE KEY INTERMEDIATE OF 1-BETA-METHYLCARBAPENEMS BY CHEMICOENZYMATIC APPROACH

被引：35

作者：

KAGA, H ^{[1
]}

KOBAYASHI, S ^{[1
]}

OHNO, M ^{[1
]}

机构：

[1] UNIV TOKYO,FAC PHARMACEUT SCI,BUNKYO KU,TOKYO 113,JAPAN

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 01期

关键词：

D O I：

10.1016/S0040-4039(01)80338-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：113 / 116

页数：4

共 10 条

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[4] A NOVEL AND EFFICIENT SYNTHESIS OF THE KEY INTERMEDIATE OF 1-BETA-METHYLCARBAPENEM ANTIBIOTICS EMPLOYING [2+2]-CYCLOADDITION REACTION OF DIKETENE WITH A CHIRAL IMINE [J].

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[5] CREATION OF NOVEL CHIRAL SYNTHONS WITH ENZYMES AND APPLICATIONS TO NATURAL PRODUCT SYNTHESIS .15. EFFICIENT INTRODUCTION OF CHIRAL CENTERS INTO CYCLOHEXANE RING [J].

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[6] CREATION OF NOVEL CHIRAL SYNTHONS WITH ENZYMES AND APPLICATIONS TO NATURAL PRODUCT SYNTHESIS .16. DIVERSIFIED SYNTHETIC APPROACHES TO THE CARBAPENEM ANTIBIOTICS BASED ON SYMMETRIZATION-ASYMMETRIZATION CONCEPT [J].

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[10] NOVEL FUNCTIONAL-GROUP SELECTIVITY IN REDUCTIONS WITH LITHIUM BOROHYDRIDE IN MIXED-SOLVENTS CONTAINING METHANOL [J].

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