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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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Direct, Metal-free C(sp2 )-H Chalcogenation of Indoles and Imidazopyridines with Dichalcogenides Catalysed by KIO3.

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.
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Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: a metal free approach.

TL;DR: The highly efficient Rose Bengal-catalysed C(sp2)-H selenylation of indoles, imidazoles and arenes was achieved using a half molar equiv.
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NH4I-catalyzed chalcogen(S/Se)-functionalization of 5-membered N-heteroaryls under metal-free conditions

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.
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Metal- and Solvent-Free Approach to Access 3-Se/S-Chromones from the Cyclization of Enaminones in the Presence of Dichalcogenides Catalyzed by KIO3

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.
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Trihaloisocyanuric acids in ethanol: an eco-friendly system for the regioselective halogenation of imidazo-heteroarenes

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.