REGIOSELECTIVE OF 1,3-DIPOLAR CYCLOADDITION OF MUNCHNONES TO ELECTROPHILIC ALKENES

被引：17
作者：
TEXIER, F
MAZARI, M
YEBDRI, O
TONNARD, F
CARRIE, R
机构：
[1] UNIV ORAN,SYNTH ORGAN LAB,ES SENIA,ALGERIA
[2] UNIV RENNES 1,PHYSICOCHIM STRUCT GRP,CNRS,URA 015,F-35042 RENNES,FRANCE
[3] UNIV RENNES 1,CNRS,URA 704,F-35042 RENNES,FRANCE
来源：
TETRAHEDRON | 1990年 / 46卷 / 10期
关键词：
D O I：
10.1016/S0040-4020(01)81520-9
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The 1,3-dipolar cycloaddition of several substituted Münchnones with methyl α-cyanocinnamate and α-cyanocinnamonitrile leads to 2-pyrrolines which may be aromatized to pyrroles. This study shows the influence of steric factors on the regioselectivity of the reaction which is "a priori" difficult to predict. © 1990.
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页码：3515 / 3526
页数：12
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