Synthesis and antioxidant activity of some new thioglycoluril derivatives

Synthesis and antioxidant activity of some new thioglycoluril derivatives

Bibliographic Details
Parent link:	Journal of Sulfur Chemistry Vol. 32, iss. 1.— 2019.— [P. 3-16]
Corporate Authors:	Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий, Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение химической инженерии
Other Authors:	Boudebouz I. Imene, Arrous S. Salah, Plotnikov E. V. Evgeny Vladimirovich, Voronova O. A. Olesya Aleksandrovna, Bakibaev A. A. Abdigali Abdimanapovich
Summary:	Title screen A series of S-alkylated products was prepared by alkylation of thioglycoluril with various alkylation agents, i.e. ethyl bromide, ethylene dibromide and chloroacetic acid. The synthesis performed in DMF at 60°C using sodium hydroxide as a base to give the corresponding products with significant advantages such as high conversions, short reaction time, mild reaction conditions, and low cost, simple workup with moderate to excellent yields. The structures of the synthesized compounds have been deduced from their spectral (IR, 1H-NMR and 13C-NMR) data. Significant antioxidant activity was observed for some members of the series. Режим доступа: по договору с организацией-держателем ресурса
Published:	2019
Subjects:	электронный ресурс труды учёных ТПУ thioglycoluril alkylation alkyl halides hioamides antioxidant activity алкилирование алкилгалогениды антиоксидантная активность
Online Access:	https://doi.org/10.1080/17415993.2019.1588897
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=661347

Internet

https://doi.org/10.1080/17415993.2019.1588897