Microwave Assisted Rapid Synthesis of (Arylselanyl)phenyl-1H-1,2,3-triazoles by Copper Catalyzed 1,3-Dipolar Cycloaddition

Title:Microwave Assisted Rapid Synthesis of (Arylselanyl)phenyl-1H-1,2,3-triazoles by Copper Catalyzed 1,3-Dipolar Cycloaddition

Volume: 3 Issue: 1

Author(s): Mauricio C.D.F. Xavier, Daiane M. Xavier, Natália Seus, Eder J. Lenardão, Gelson Perin and Diego Alves

Affiliation:

Keywords: Alkynes, azides, catalysis, 1, 3-dipolar, click chemistry, copper, cycloaddition, green chemistry, heterocycles, microwave, 1, 2, 3-triazoles, nitrogen compounds, selanyltriazoles, selenium compounds.

Abstract: We describe here a simple and rapid protocol for the synthesis of (arylselanyl)phenyl-1H- 1,2,3-triazoles by copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions using Microwave Irradiation. The products were obtained under mild conditions in excellent yields in a short reaction time by reacting azidophenyl arylselenides with a range of terminal alkynes using catalytic amount of Cu(OAc)2.H2O/sodium ascorbate. This Click Chemistry protocol is an efficient method to synthesize new selenium compounds with potential application in biological studies and materials sciences.

Cite this article as:

Xavier C.D.F. Mauricio, Xavier M. Daiane, Seus Natália, Lenardão J. Eder, Perin Gelson and Alves Diego, Microwave Assisted Rapid Synthesis of (Arylselanyl)phenyl-1H-1,2,3-triazoles by Copper Catalyzed 1,3-Dipolar Cycloaddition, Current Microwave Chemistry 2016; 3 (1) . https://dx.doi.org/10.2174/2213335602666150119221147