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Jamal Rafique

Researcher at Federal University of Mato Grosso do Sul

Publications -  72
Citations -  1752

Jamal Rafique is an academic researcher from Federal University of Mato Grosso do Sul. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 22, co-authored 59 publications receiving 1157 citations. Previous affiliations of Jamal Rafique include University of Karachi & Universidade Federal de Santa Catarina.

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Regioselective, Solvent- and Metal-Free Chalcogenation of Imidazo[1,2-a]pyridines by Employing I2/DMSO as the Catalytic Oxidation System

TL;DR: The current protocol was also extended to other N-heterocyclic cores and allowed the preparation of different types of chalcogenated imidazo[1,2-a]pyridines with structural diversity.
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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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Aflatoxin M1 in human breast milk: A global systematic review, meta-analysis, and risk assessment study (Monte Carlo simulation)

TL;DR: With increasing average rain annual and poverty (GDP ranking), the prevalence of AFM1 in human breast milk significantly increases significantly and the probabilistic carcinogenic risk by the hazard index (HI) in the Monte Carlo simulation (MCS) is calculated.
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DMSO/iodine-catalyzed oxidative C–Se/C–S bond formation: a regioselective synthesis of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes

TL;DR: In this paper, a convenient metal-free and solvent-free iodine-catalyzed regioselective greener protocol to access different types of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes through direct C(sp2)-H bond activation was developed.