ALPHA-AMINO-ACIDS AS CHIRAL EDUCTS FOR STEREOSELECTIVE SYNTHESES OF PYRROLIDINE AND PYRROLIZIDINE SYSTEMS

被引：36

作者：

CHIACCHIO, U ^{[1
]}

CASUSCELLI, F ^{[1
]}

CORSARO, A ^{[1
]}

LIBRANDO, V ^{[1
]}

RESCIFINA, A ^{[1
]}

ROMEO, R ^{[1
]}

ROMEO, G ^{[1
]}

机构：

[1] UNIV MESSINA,DIPARTIMENTO FARMACOCHIM,I-98168 MESSINA,ITALY

来源：

TETRAHEDRON | 1995年 / 51卷 / 19期

关键词：

D O I：

10.1016/0040-4020(95)00233-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Homochiral functionalized pyrrolidine and pyrrolizidine systems have been achieved by stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral nitrones, starting from homochiral amino acids, and by subsequent reduction of the obtained cycloadducts.

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收藏

页码：5689 / 5700

页数：12

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