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

引用

页码：975 / 979

页数：5

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