STEREOSELECTIVE CYCLOADDITIONS OF ACYL-NITROSO COMPOUNDS - AN APPROACH TO CARBAPENEM SYNTHESIS

被引：17

作者：

MORLEY, AD

HOLLINSHEAD, DM

PROCTER, G

机构：

[1] UNIV SALFORD,DEPT CHEM & APPL CHEM,SALFORD M5 4WT,LANCS,ENGLAND

[2] ICI PHARMACEUT PLC,MACCLESFIELD SK10 4TG,CHESHIRE,ENGLAND

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 07期

关键词：

D O I：

10.1016/S0040-4039(00)94427-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The adduct obtained from cyclopentadiene and benzohydroxamic acid under oxidising conditions has been used in a stereoselective synthesis of the N-benzoyl derivative of a known intermediate for carbapenem synthesis. © 1990.

引用

页码：1047 / 1050

页数：4

共 12 条

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[6] SYNTHETIC APPLICATION OF PHENYLTHIOMETHYL AND PHENYLSULFONYLMETHYL ETHERS TO ALDEHYDES, METHYLALS, CARBOXYLIC-ACIDS, AND ENOL OR DIENOL ETHERS
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[10] THE EFFICIENT CONSECUTIVE BETA-CARBOXYLATION AND ALPHA-ALKYLATION OF CYCLIC ALPHA,BETA-ENONES - A NEW ROUTE TO SARKOMYCIN
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