Catalytic alkylation of cycloalkaneindoles and tetrahydro-γ-carboline with 9-oxiranylmethylcarbazole


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

Catalytic alkylation of substituted indoles such as cycloalkaneindoles and tetrahydro-γ-carboline using 9-oxiranylmethylcarbazole leads to the formation of 1-(carbazol-9-yl)-3-{dihydrocycloalkane[b]indol-4(1H)-yl}propan-2-ols and 1-(carbazol-9-yl)-3-{2,8-dimethyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl}propan-2-ol, conjugates containing 2-hydroxypropylene spacer.

作者简介

V. Sokolov

Institute of Physiologically Active Compounds

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severniy pr. 1, Chernogolovka, 142432

A. Aksinenko

Institute of Physiologically Active Compounds

编辑信件的主要联系方式.
Email: alaks@ipac.ac.ru
俄罗斯联邦, Severniy pr. 1, Chernogolovka, 142432

T. Epishina

Institute of Physiologically Active Compounds

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severniy pr. 1, Chernogolovka, 142432

T. Goreva

Institute of Physiologically Active Compounds

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severniy pr. 1, Chernogolovka, 142432


版权所有 © Pleiades Publishing, Ltd., 2016
##common.cookie##