CYCLOADDITION OF N-PHENYLMALEIMIDE TO (1,2,3,6-TETRAHYDROPYRIDYL)-INDOLE

被引:8
作者
BECK, D
SCHENKER, K
机构
[1] Chemische Forschungslaboratorien des Departementes Pharmazeutika, CIBA AKTIENGESELLSCHAFT, Basel
关键词
D O I
10.1002/hlca.19680510205
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
1‐Methyl‐2‐and 1‐methyl‐3‐(1‐methyl‐1,2,3,6‐tetrahydro‐4‐pyridyl)‐indole undergo 1,4‐cycloaddition (formally of the DIELS‐ALDER‐type) with N‐phenyl‐maleimide, leading to the pentacyclic compounds III and IV. Copyright © 1968 Verlag GmbH & Co. KGaA, Weinheim
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页码:264 / &
相关论文
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HELVETICA CHIMICA ACTA, 1968, 51 (02) :260-&
[2]  
BECK D, 1967, ANGEW CHEM, V79, P984
[3]  
NOLAND WE, 1963, J ORG CHEM, V28, P884
[4]   THE SYNTHESIS OF CARBAZOLES FROM 3-VINYLINDOLES WITH TETRACYANOETHYLENE AND DIMETHYL ACETYLENEDICARBOXYLATE [J].
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