A Green Approach to 2-Substituted Benzo- and Naphthothiazoles via <i>N</i>-bromosuccinimide/Bromide-Mediated C(aryl)-S Bond Formation

2-Substituted benzo- and naphthothiazoles have been conveniently prepared from the intramolecular cyclization of phenylthioureas and activated thiobenzanilides or the coupling of isothiocyanates with amines under mild conditions using <i>N</i>-bromosuccinimide/tetrabutylammonium bromide in 1,2-dimet...

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Autores principales:	Ainka T. Brown, Nadale K. Downer-Riley
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	MDPI AG 2022-11-01
Colección:	Molecules
Materias:	2-aminobenzothiazole benzothiazole <i>N</i>-bromosuccinimide naphthothiazole oxidative cyclization phenylthiourea
Acceso en línea:	https://www.mdpi.com/1420-3049/27/22/7876
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