Synthesis of New 2-(Oxiran-2-yl)-1,3-oxazoles


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

Reaction of 2-chloro-N-(2,2-dichloro-1-cyanovinyl)acetamide with dimethylamine gave 5-(dimethylamino)-2-[(dimethylamino)methyl]-1,3-oxazole-4-carbonitrile, where aliphatic dimethylamino group was regioselectively alkylated with iodomethane. The resulting trimethylammonium salt reacted diastereoselectively with aromatic aldehydes to form new substituted 2-(oxiran-2-yl)-1,3-oxazoles.

作者简介

O. Shablykin

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
乌克兰, ul. Murmanskaya 1, Kyiv, 02094

M. Volosheniuk

Taras Shevchenko National University of Kyiv

Email: brovarets@bpci.kiev.ua
乌克兰, Kyiv

V. Brovarets

Institute of Bioorganic Chemistry and Petrochemistry

编辑信件的主要联系方式.
Email: brovarets@bpci.kiev.ua
乌克兰, ul. Murmanskaya 1, Kyiv, 02094


版权所有 © Pleiades Publishing, Ltd., 2018
##common.cookie##