@article {44369,
	title = {Visible-light-mediated eosin Y photoredox-catalyzed vicinal thioamination of alkynes: radical cascade annulation strategy for 2-substituted-3-sulfenylindoles},
	journal = {European Journal of Organic Chemistry},
	year = {2018},
	month = {MAY},
	pages = {2117-2121},
	type = {Article},
	abstract = {An organic dye photoredox-catalyzed regiospecific radical cascade annulation strategy of 2-alkynyl-azidoarenes to generate 3-sulfenylindoles via vicinal thioamination of alkynes at room temperature, mediated by visible light, was developed. The method requires mild conditions, including visible light as a traceless green energy source, room temperature, eosin Y organic dye as a photoredox catalyst, ambient air as oxidant, and easily available starting materials to provide a green, efficient, metal- and strong-oxidant-free synthesis of 3-sulfenylindoles with broad substrate scope through vicinal thioamination of alkynes.},
	doi = {10.1002/ejoc.201800287},
	author = {Tambe, Shrikant D. and Rohokale, Rajendra S. and Kshirsagar, Umesh A.}
}
