Efficient one-pot synthesis of substituted diphenyl 1, 3-thiazole through multicomponent reaction by using green and efficient Iron-catalyst via Cross-Dehydrogenative Coupling(CDC)

dc.contributor.author	Singh M.; Yadav V.B.; Ansari M.D.; Malviya M.; Siddiqui I.R.
dc.date.accessioned	2025-05-23T11:23:09Z
dc.description.abstract	Abstract: A clean and efficient, multi-component strategy for the synthesis of biologically important trisubstituted thiazole via the reaction of readily available barbituric acid, acetophenone, and aryl thioamides is reported in the presence of FeCl3.6H2O / O2(Air) in DMF solvent. The advantages of the present methodology include a one-pot reaction, environment-friendly approach, cost-effectiveness, broad substrate scope, operational simplicity, short reaction time, easy workup procedure, and high yields. Graphic Abstract: [Figure not available: see fulltext.] © 2021, The Author(s), under exclusive licence to Springer Nature Switzerland AG part of Springer Nature.
dc.identifier.doi	https://doi.org/10.1007/s11030-021-10191-w
dc.identifier.uri	http://172.23.0.11:4000/handle/123456789/8729
dc.relation.ispartofseries	Molecular Diversity
dc.title	Efficient one-pot synthesis of substituted diphenyl 1, 3-thiazole through multicomponent reaction by using green and efficient Iron-catalyst via Cross-Dehydrogenative Coupling(CDC)

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