Unexpected synthesis and crystal structure of N-2-[2-(2-acetylethenyl)phenoxy]ethyl-N-ethenyl-4-methylbenzenesulfonamideстатья
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Дата последнего поиска статьи во внешних источниках: 20 апреля 2022 г.
Авторы:
Temesgen A.W. ,
Luong M.D. ,
Truong H.H. ,
Nguyen V.T.,
Dang T.T.A ,
Le T A. ,
Tskhovrebov A.G. ,
Khrustalev V.N.
Журнал:
Acta Crystallographica Section E Crystallographic Communications
Том:
76
Год издания:
2020
Издательство:
International Union of Crystallography
Местоположение издательства:
United Kingdom
Первая страница:
1851
Последняя страница:
1853
DOI:
10.1107/S2056989020015194
Аннотация:
The title compound, C21H23NO4S, obtained by alkaline treatment of 1,5-bis(1-phenoxy)-3-azapentane at moderate heating, is a N-tosylated secondary vinylamine. An intramolecular S=O⋯H - C hydrogen bond generates a 13-membered ring. The benzalacetone moiety adopts a trans conformation with respect to the C=C double bond, which is slightly longer than usual due to the conjugation with a neighbouring acetyl group. Theoretical predictions of potential biological activities were performed, suggesting that the title compound can inhibit gluconate 2-dehydrogenase (85% probability), as well as to act as a mucomembranous protector (73%). © 2020.
Добавил в систему:
Цховребов Александр Георгиевич