Eosin Y-Catalyzed Synthesis of 3-Aminoimidazo[1,2- a]Pyridines via the HAT Process under Visible Light through Formation of the C-N Bond

dc.contributor.author	Singh, H.K.
dc.contributor.author	Kamal, A.
dc.contributor.author	Kumari, S.
dc.contributor.author	Kumar, D.
dc.contributor.author	Maury, S.K.
dc.contributor.author	Srivastava, V.
dc.contributor.author	Singh, S.
dc.date.accessioned	2020-12-11T06:03:08Z
dc.date.available	2020-12-11T06:03:08Z
dc.date.issued	2020
dc.identifier.issn	24701343
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/1137
dc.description.abstract	A comfortable, environment-friendly, and metal-free approach for synthesizing the biologically important moiety aminoimidazopyridine through the multicomponent reaction of benzylamine, 2-aminopyridine, and t-butyl isocyanide under visible light using eosin Y as a photocatalyst has been developed. Inexpensive, nontoxic, the effortless accessibility of starting materials, and nonparticipation of particular glassware and a photoreactor system are important qualities of the current approach. Strangely, the mild conditions, environment-friendly, and enumerating tolerance of an extensive range of both electron-donating and electron-withdrawing groups are additional features of the approach. ©	en_US
dc.language.iso	en_US	en_US
dc.publisher	American Chemical Society	en_US
dc.relation.ispartofseries	ACS Omega;
dc.title	Eosin Y-Catalyzed Synthesis of 3-Aminoimidazo[1,2- a]Pyridines via the HAT Process under Visible Light through Formation of the C-N Bond	en_US
dc.type	Article	en_US