SYNTHESIS OF NEW ANNELATED INDOLE SYSTEMS - NEW ENTRY IN THE E-AZAEBURNANE SERIES

被引：22
|
作者：
MELNYK, P [1 ]
LEGRAND, B [1 ]
GASCHE, J [1 ]
DUCROT, P [1 ]
THAL, C [1 ]
机构：
[1] CNRS,INST CHIM SUBST NAT,F-91198 GIF SUR YVETTE,FRANCE
来源：
TETRAHEDRON | 1995年 / 51卷 / 07期
关键词：
D O I：
10.1016/0040-4020(94)01075-B
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Starting from a judiciously substituted N-aminoindole, the Heck reaction led to new classes of heterocyclic compounds: the pyrido[2',3'-d']pyridazino[2,3-a]indoles 7 and 8 and the pyrido[2',3'-d']diazepino[1,6,7-h,i]indole 15. From compound 7 the pentacyclic E-azaeburnane 21 was prepared.
引用
收藏
页码：1941 / 1952
页数：12
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