Synthesis and Some Transformations of (2,2-Dimethyl-4-propyltetrahydro-2H-pyran-4-yl)acetonitrile


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

Removal of the ethoxycarbonyl group in ethyl cyano-(2,2-dimethyl-4-propyltetrahydro-2H-pyran-4 -yl)acetate afforded the corresponding (2,2-dimethyl-4-propyltetrahydro-2H-pyran-4-yl)acetonitrile. The reduction of the latter with lithium aluminum hydride furnished 2-(2,2-dimethyl-4-propyltetrahydro-2H-pyran- 4-yl)ethanamine, which reacted with furfural and a heterocyclic ketone followed by reduction to form the secondary amines and some amides. Hydrolysis of the above nitrile resulted in the corresponding acid, which was converted in a series of amides.

作者简介

N. Arutyunyan

Mnjoyan Institute of Fine Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry

Email: gyulgev@gmail.com
亚美尼亚, pr. Azatutyan 26, Yerevan, 0014

L. Akopyan

Mnjoyan Institute of Fine Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry

Email: gyulgev@gmail.com
亚美尼亚, pr. Azatutyan 26, Yerevan, 0014

N. Akopyan

Mnjoyan Institute of Fine Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry

Email: gyulgev@gmail.com
亚美尼亚, pr. Azatutyan 26, Yerevan, 0014

G. Panosyan

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

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

G. Gevorgyan

Mnjoyan Institute of Fine Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry

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


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