Your browser doesn't support javascript.
loading
Synthesis of Biologically Relevant 1,2,3- and 1,3,4-Triazoles: From Classical Pathway to Green Chemistry.
Gonnet, Lori; Baron, Michel; Baltas, Michel.
Afiliação
  • Gonnet L; IMT Mines Albi, UMR CNRS 5302, Centre Rapsodee, Campus Jarlard, Allée des Sciences, Université de Toulouse, CEDEX 09, 81013 Albi, France.
  • Baron M; Department of Chemistry, McGill University, 801 Sherbrooke St. West, Montreal, QC H3A 0B8, Canada.
  • Baltas M; IMT Mines Albi, UMR CNRS 5302, Centre Rapsodee, Campus Jarlard, Allée des Sciences, Université de Toulouse, CEDEX 09, 81013 Albi, France.
Molecules ; 26(18)2021 Sep 18.
Article em En | MEDLINE | ID: mdl-34577138
ABSTRACT
Green Chemistry has become in the last two decades an increasing part of research interest. Nonconventional «green¼ sources for chemical reactions include micro-wave, mechanical mixing, visible light and ultrasound. 1,2,3-triazoles have important applications in pharmaceutical chemistry while their 1,2,4 counterparts are developed to a lesser extent. In the review presented here we will focus on synthesis of 1,2,3 and 1,2,4-triazole systems by means of classical and « green chemistry ¼ conditions involving ultrasound chemistry and mechanochemistry. The focus will be on compounds/scaffolds that possess biological/pharmacophoric properties. Finally, we will also present the formal cycloreversion of 1,2,3-triazole compounds under mechanical forces and its potential use in biological systems.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triazóis Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triazóis Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França