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Mechanochemical Solvent-Free One-Pot Synthesis of Poly-Functionalized 5-(Arylselanyl)-1H-1,2,3-triazoles Through a Copper(I)-Catalyzed Click Reaction.
Karmakar, Pintu; Karmakar, Indrajit; Mukherjee, Debojyoti; Bhowmick, Anindita; Brahmachari, Goutam.
Afiliación
  • Karmakar P; Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Visva-Bharati (a Central University), 731 235, Santiniketan, West Bengal, India.
  • Karmakar I; Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Visva-Bharati (a Central University), 731 235, Santiniketan, West Bengal, India.
  • Mukherjee D; Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Visva-Bharati (a Central University), 731 235, Santiniketan, West Bengal, India.
  • Bhowmick A; Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Visva-Bharati (a Central University), 731 235, Santiniketan, West Bengal, India.
  • Brahmachari G; Laboratory of Natural Products & Organic Synthesis, Department of Chemistry, Visva-Bharati (a Central University), 731 235, Santiniketan, West Bengal, India.
Chemistry ; 29(63): e202302539, 2023 Nov 13.
Article en En | MEDLINE | ID: mdl-37665692
ABSTRACT
A mechanochemistry-driven practical and efficient synthetic protocol for accessing diverse series of biologically relevant poly-functionalized 5-(arylselanyl)-1H-1,2,3-triazoles through copper(I)-catalyzed click reaction between aryl/heteroaryl acetylenes, diaryl diselenides, benzyl bromides, and sodium azide has been accomplished under high-speed ball-milling. Advantages of this method include operational simplicity, avoidance of using solvent and external heating, one-pot synthesis, short reaction time in minutes, good to excellent yields, broad substrate scope, and gram-scale applications. Furthermore, synthesized organoselenium compounds were synthetically diversified to biologically promising selenones.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: India
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