SYNTHESIS OF 3,9B-DIHYDRO-5H-PYRROLO[2,1-A]ISOINDOLES AND 3,5,6,10B-TETRAHYDROPYRROLO[2,1-A]ISOQUINOLINES WITH 1,3-DIPOLAR CYCLOADDITION REACTIONS

被引：14
|
作者：
ANDERSON, WK
KINDER, FR
机构：
[1] Department of Medicinal Chemistry, School of Pharmacy, State University of New York at Buffalo, Buffalo, New York
来源：
JOURNAL OF HETEROCYCLIC CHEMISTRY | 1990年 / 27卷 / 04期
关键词：
D O I：
10.1002/jhet.5570270428
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The title classes of compounds have been prepared using a sequence of two ring‐forming reactions. Initial 1,3‐dipolar cycloaddition with an azomethine ylide gave N‐acylated 3‐pyrrolines which were further elaborated to the target compounds by a tandem deprotection/cyclization reaction. Copyright © 1990 Journal of Heterocyclic Chemistry
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页码：975 / 979
页数：5
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