M
Marcelo S. Franco
Researcher at Universidade Federal de Santa Catarina
Publications - 7
Citations - 363
Marcelo S. Franco is an academic researcher from Universidade Federal de Santa Catarina. The author has contributed to research in topics: Indazole & Atom economy. The author has an hindex of 6, co-authored 7 publications receiving 227 citations.
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Journal ArticleDOI
Direct, Metal-free C(sp2 )-H Chalcogenation of Indoles and Imidazopyridines with Dichalcogenides Catalysed by KIO3.
Jamal Rafique,Sumbal Saba,Marcelo S. Franco,Luana Bettanin,Alex R. Schneider,Lais T. Silva,Antonio L. Braga +6 more
TL;DR: A greener protocol for the synthesis of 3-Se/S-indoles and imidazo[1,2-a]pyridines through direct C(sp2 )-H bond chalcogenation of heteroarenes with half molar equivalents of different dichalCogenides, using KIO3 as a non-toxic, easy-to-handle catalyst and a stoichiometric amount of glycerol.
Journal ArticleDOI
Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: a metal free approach.
Sumbal Saba,Jamal Rafique,Marcelo S. Franco,Alex R. Schneider,Leandro Espíndola,Dagoberto de O. Silva,Antonio L. Braga +6 more
TL;DR: The highly efficient Rose Bengal-catalysed C(sp2)-H selenylation of indoles, imidazoles and arenes was achieved using a half molar equiv.
Journal ArticleDOI
NH4I-catalyzed chalcogen(S/Se)-functionalization of 5-membered N-heteroaryls under metal-free conditions
Luana Bettanin,Sumbal Saba,Carlos V. Doerner,Marcelo S. Franco,Marcelo Godoi,Jamal Rafique,Antonio L. Braga +6 more
TL;DR: In this paper, the NH4I-catalyzed C H bond chalcogenation of N-heteroaryls in the presence of a minimum amount of DMSO/H2O/acetic acid as additives was described.
Journal ArticleDOI
Metal- and Solvent-Free Approach to Access 3-Se/S-Chromones from the Cyclization of Enaminones in the Presence of Dichalcogenides Catalyzed by KIO3
Jamal Rafique,Sumbal Saba,Sumbal Saba,Alex R. Schneider,Marcelo S. Franco,Symara M. Silva,Antonio L. Braga +6 more
TL;DR: A greener protocol for the one-pot synthesis of 3-Se/S-4H-chromen-4-ones using 2-hydroxyphenyl enaminones and half equivalents of various odorless diorganyl dichalcogenides (S/Se) in the presence of glycerol and KIO3 under solvent-free conditions.
Journal ArticleDOI
Trihaloisocyanuric acids in ethanol: an eco-friendly system for the regioselective halogenation of imidazo-heteroarenes
José S. S. Neto,Renata A. Balaguez,Marcelo S. Franco,Victor C. de Sá Machado,Sumbal Saba,Jamal Rafique,Fábio Z. Galetto,Antonio L. Braga +7 more
TL;DR: An efficient, rapid and benign protocol for the direct C(sp2)–H bond halogenation of 2-arylimidazo[1,2-a]pyridines using trihaloisocyanuric acids in ethanol was successfully extended to imidazopyrimidine,Imidazothiazole and indazole heterocycles showing the broadness of this useful approach.