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Green Approach for the Synthesis of Chalcogenyl- 2,3-dihydrobenzofuran Derivatives Through Allyl-phenols/ Naphthols and Their Potential as MAO-B Inhibitors.
Azevedo, Amanda R; Cordeiro, Pâmella; Strelow, Dianer N; de Andrade, Karine N; Neto, Marcos R S; Goetze Fiorot, Rodolfo; Brüning, César A; Braga, Antonio L; Lião, Luciano M; Bortolatto, Cristiani F; Neto, José S S; Nascimento, Vanessa.
Afiliação
  • Azevedo AR; SupraSelen Laboratory, Department of Organic Chemistry, Universidade Federal Fluminense, Niterói, Institute of Chemistry, Campus do Valonguinho, 24020-141, RJ, Brazil.
  • Cordeiro P; SupraSelen Laboratory, Department of Organic Chemistry, Universidade Federal Fluminense, Niterói, Institute of Chemistry, Campus do Valonguinho, 24020-141, RJ, Brazil.
  • Strelow DN; Molecular Biochemistry and Neuropharmacology Laboratory (LABIONEM), Chemical, Pharmaceutical and Food Sciences Center (CCQFA), Federal University of Pelotas Pelotas, 96010-900, RS, Brazil.
  • de Andrade KN; Department of Organic Chemistry, Institute of Chemistry, Universidade Federal Fluminense Niterói, Outeiro São João Batista, s/n, 24020-141, RJ, Brazil.
  • Neto MRS; LabSelen, Department of Chemistry, Federal University of Santa Catarina, Santa Catarina, 88040-900, SC, Brazil.
  • Goetze Fiorot R; Department of Organic Chemistry, Institute of Chemistry, Universidade Federal Fluminense Niterói, Outeiro São João Batista, s/n, 24020-141, RJ, Brazil.
  • Brüning CA; Molecular Biochemistry and Neuropharmacology Laboratory (LABIONEM), Chemical, Pharmaceutical and Food Sciences Center (CCQFA), Federal University of Pelotas Pelotas, 96010-900, RS, Brazil.
  • Braga AL; LabSelen, Department of Chemistry, Federal University of Santa Catarina, Santa Catarina, 88040-900, SC, Brazil.
  • Lião LM; LabRMN, Chemistry Institute, Federal University of Goiás Goiânia, 74690-900, GO, Brazil.
  • Bortolatto CF; Molecular Biochemistry and Neuropharmacology Laboratory (LABIONEM), Chemical, Pharmaceutical and Food Sciences Center (CCQFA), Federal University of Pelotas Pelotas, 96010-900, RS, Brazil.
  • Neto JSS; LabRMN, Chemistry Institute, Federal University of Goiás Goiânia, 74690-900, GO, Brazil.
  • Nascimento V; SupraSelen Laboratory, Department of Organic Chemistry, Universidade Federal Fluminense, Niterói, Institute of Chemistry, Campus do Valonguinho, 24020-141, RJ, Brazil.
Chem Asian J ; 18(24): e202300586, 2023 Dec 14.
Article em En | MEDLINE | ID: mdl-37733585
This work presents the design, synthesis, and MAO-B inhibitor activity of a series of chalcogenyl-2,3-dihydrobenzofurans derivatives. Using solvent- and metal-free methodology, a series of chalcogen-containing dihydrobenzofurans 7-9 was obtained with yields ranging from 40% to 99%, using an I2 /DMSO catalytic system. All compounds were fully structurally characterized using 1 H and 13 C NMR analysis, and the unprecedented compounds were additionally analyzed using high-resolution mass spectrometry (HRMS). In addition, the mechanistic proposal that iodide is the most likely species to act in the transfer of protons along the reaction path was studied through theoretical calculations. Finally, the compounds 7b-e, 8a-e, and 9a showed great promise as inhibitors against MAO-B activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil País de publicação: Alemanha