Stevens rearrangement of unsaturated ammonium salts. Synthesis of substituted furans


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

Ammonium salts bearing but-2-ynyl and phenacyl or 2-(naphth-2-yl)-2-oxoethyl moieties at the nitrogen atom underwent Stevens rearrangement to form substituted furan-3-amines. Quaternization of the latter afforded appropriate iodomethylates.

作者简介

M. Manukyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

编辑信件的主要联系方式.
Email: manukyanmeri@gmail.com
亚美尼亚, pr. Azatutyana 26, Yerevan, 0014

T. Sahakyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
亚美尼亚, pr. Azatutyana 26, Yerevan, 0014

A. Gyulnazaryan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
亚美尼亚, pr. Azatutyana 26, Yerevan, 0014

A. Babakhanyan

Abovyan Armenian State Pedagogical University

Email: manukyanmeri@gmail.com
亚美尼亚, Yerevan

N. Minasyan

Molecular Structure Research Center, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
亚美尼亚, Yerevan

K. Barseghyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
亚美尼亚, pr. Azatutyana 26, Yerevan, 0014


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