TRANS-3-ARYL-4-NITRO-PYRROLIDINES VIA 1,3-DIPOLAR CYCLOADDITION OF NONSTABILIZED AZOMETHINE YLIDE TO BETA-NITRO STYRENES

被引：33

作者：

NYERGES, M ^{[1
]}

BALAZS, L ^{[1
]}

KADAS, I ^{[1
]}

BITTER, I ^{[1
]}

KOVESDI, I ^{[1
]}

TOKE, L ^{[1
]}

机构：

[1] TECH UNIV BUDAPEST,HUNGARIAN ACAD SCI,RES GRP,DEPT ORGAN CHEM TECHNOL,H-1521 BUDAPEST,HUNGARY

来源：

TETRAHEDRON | 1995年 / 51卷 / 24期

关键词：

D O I：

10.1016/0040-4020(95)00311-U

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Various beta-nitro styrenes undergo 1,3 dipolar cycloaddition with the azomethine ylide derived from sarcosine and paraformaldehyde to give 3-aryl-4-nitro-pyrrolidines in good yield.

引用

页码：6783 / 6788

页数：6

共 30 条

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