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Intramolecular Click Cycloaddition Reactions: Synthesis of 1,2,3-Triazoles.
Tashrifi, Zahra; Khanaposhtani, Mohammad Mohammadi; Bahadorikhalili, Saeed; Larijani, Bagher; Mahdavi, Mohammad.
Afiliación
  • Tashrifi Z; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Khanaposhtani MM; Faculty of Fouman, College of Engineering, University of Tehran, Fouman, Iran.
  • Bahadorikhalili S; Department of Electronic Engineering, Universitat Rovira i Virgili, 43007 Tarragona, Spain.
  • Larijani B; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Mahdavi M; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Curr Org Synth ; 21(2): 166-194, 2024.
Article en En | MEDLINE | ID: mdl-37026493
ABSTRACT
Click Chemistry, as a powerful tool, has been used for the synthesis of a variety of 1,2,3-triazoles. Among click cycloaddition reactions, intramolecular click reactions carried out in azido-alkyne precursors has not been thoroughly reviewed. Hence, in this review, we have summarized and categorised the recent literature (from 2012 on) based on the azidoalkynyl precursor's type and a brief and concise description of the involved mechanisms is presented. Accordingly, we have classified the relevant literature into three categories (1) substitution precursors (2) addition and (3) multi-component reaction (MCR) products.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Curr Org Synth Año: 2024 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Curr Org Synth Año: 2024 Tipo del documento: Article País de afiliación: Irán