HIGHLY DIASTEREOSELECTIVE INTRAMOLECULAR NITRONE CYCLO-ADDITIONS TO ALPHA,BETA-UNSATURATED ESTERS

被引：21

作者：

ANNUNZIATA, R ^{[1
]}

CINQUINI, M ^{[1
]}

COZZI, F ^{[1
]}

RAIMONDI, L ^{[1
]}

机构：

[1] UNIV MILAN,DIPARTIMENTO CHIM ORGAN & IND,I-20133 MILANO,ITALY

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 23期

关键词：

D O I：

10.1016/0040-4039(88)85237-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2881 / 2884

页数：4

共 15 条

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[4]

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[5] HIGHLY STEREOCONTROLLED SYNTHESIS OF THE KEY INTERMEDIATE OF 1-BETA-METHYLCARBAPENEM ANTIBIOTIC VIA INTRAMOLECULAR NITRONE 1,3-DIPOLAR CYCLO-ADDITION [J].

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[9] ASYMMETRIC-SYNTHESIS OF 4-ACETOXY-3-HYDROXYETHYLAZETIDIN-2-ONE, A KEY INTERMEDIATE FOR THE PREPARATION OF PENEM AND CARBAPENEM ANTIBIOTICS [J].

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[10] FURTHER-STUDIES ON THE SYNTHESIS OF THIENAMYCIN - A FACILE AND STEREOSELECTIVE SYNTHESIS OF A BICYCLIC BETA-KETO ESTER BY 1,3-DIPOLAR CYCLOADDITION [J].

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