Reaction of 1,2,3,4-tetrahydro-isoquinoline enamines with quinones

被引：0

作者：

Polygalova N.N. ^{[1
]}

Mikhailovskii A.G. ^{[1
]}

Vakhrin M.I. ^{[1
]}

机构：

[1] Perm State Pharmaceutical Academy

来源：

Chem. Heterocycl. Compd. | 2006年 / 10卷 / 1352-1357期

关键词：

1,2,3,4- tetrahydroisoquinoline enamines; 2,3-dichloro-1,4-naphthoquinone; Benzo[g]naphtho[2,3-b]indolyzine-8,13-diones; Donor-acceptor complexes; Indolo[2,1-a]isoquinoline; Michael addition; Nenicescu reaction; p-benzoquinone;

D O I：

10.1007/s10593-006-0248-2

中图分类号：

学科分类号：

摘要：

The reaction of p-benzoquinone with enamino amides derived from 2,2-dimethyl-1,2,3,4-tetrahydrobenzo[f]isoquinoline proceeds through a Michael addition. The reaction of this quinone with the base of drotaverine leads to a derivative of indolo[2,1-a]isoquinoline. Fusion of isoquinoline enamines by the action of 2,3-dichloro-1,4-naphthoquinone leads to pentacyclic benzo[g]naphtho-[2,3-b]indolyzine-8,13-dione. © 2006 Springer Science+Business Media, Inc.

引用

页码：1352 / 1357

页数：5

共 46 条

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