Electrochemical oxidative selenylation of imidazo[1,2-a]pyridines with diselenides

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초록

Electrochemical oxidative selenylation of imidazo[1,2-a]pyridines has been developed. The reaction proceeds in an undivided electrochemical cell equipped with glassy carbon electrodes employing LiClO4 as a supporting electrolyte. This approach is environmentally benign by using shelf-stable diselenides as selenium source and electrons as oxidizing reagents. The present protocol offers a facile way to prepare 3-selenylated imidazopyridine derivatives. (C) 2019 Elsevier Ltd. All rights reserved.

키워드

Selenylation; Electrochemical oxidation; Imidazo[1,2-a]pyridines; 3-Selenylated imidazopyridines; CATALYZED ONE-POT; C-H AMINATION; ASYMMETRIC-SYNTHESIS; MIGRATION SEQUENCES; RING EXPANSION; IMIDAZOHETEROCYCLES; SELENIUM; IMIDAZOPYRIDINES; INHIBITORS; TETRAHYDROQUINOLINES
제목
Electrochemical oxidative selenylation of imidazo[1,2-a]pyridines with diselenides
저자
Kim, Yeon Joo; Kim, Dae Young
DOI
10.1016/j.tetlet.2019.02.001
발행일
2019-03-07
유형
Article
저널명
Tetrahedron Letters
권
60
호
10
페이지
739 ~ 742