Approach to preparative synthesis of ortho-(1-methylbut-2-en-1-yl)anilines, precursors of new cytotoxic heterocycles


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

The reaction of aromatic Claisen rearrangement of N-(1-methylbut-2-en-1-yl)anilines in the presence of p-toluenesulfonic acid was investigated. N-Tosyl-2-(1-iodoethyl)-3-methylindoline derivatives were obtained; one of them exhibited a cytotoxic activity.

作者简介

L. Aleksandrova

Ufa Institute of Chemistry of the Russian Academy of Sciences

Email: gataullin@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

M. Abdullin

Ufa Institute of Chemistry of the Russian Academy of Sciences

Email: gataullin@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

Yu. Vakhitova

Institute of Biochemistry and Genetics of Ufa Scientific Center

Email: gataullin@anrb.ru
俄罗斯联邦, Ufa

R. Gataullin

Ufa Institute of Chemistry of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: gataullin@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054


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