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COPPER NANOPARTICLE CATALYZED REGIOSELECTIVE CYCLOADDITION OF TERMINAL ACETYLENES TO SODIUM AZIDE IN THE PRESENCE OF O-TOSYL FLUOROCARBOHYDRATE DERIVATIVES: ASSEMBLY OF NOVEL ENANTIOPURE FLUOROMONOSACCHARIDES WITH 1,2,3-TRIAZOLE AND 4-PHENYL-OXAZOLIDIN-2-ONE SUBUNITS
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COPPER NANOPARTICLE CATALYZED REGIOSELECTIVE CYCLOADDITION OF TERMINAL ACETYLENES TO SODIUM AZIDE IN THE PRESENCE OF O-TOSYL FLUOROCARBOHYDRATE DERIVATIVES: ASSEMBLY OF NOVEL ENANTIOPURE FLUOROMONOSACCHARIDES WITH 1,2,3-TRIAZOLE AND 4-PHENYL-OXAZOLIDIN-2-ONE SUBUNITS

Ahlem Guesmi and Naoufel Ben Hamadi
Macedonian Journal of Chemistry and Chemical Engineering, Vol.35(1), pp.39-44
01/01/2016

Abstract

Chemistry Chemistry, Multidisciplinary Engineering Engineering, Chemical Physical Sciences Science & Technology Technology
A three-component reaction of O-tosyl carbohydrate derivatives with sodium azide and terminal alkynes can be catalyzed by copper nanoparticles under ambient conditions. A series of 1,4-disubstituted-1,2,3-triazoles were obtained regioselectively by this one-pot strategy in good to excellent yields (70-90%). The salient features of the present protocol are mild reaction conditions, a shorter reaction time, and its applicability to a wide range of substrates.
url
https://doi.org/10.20450/mjcce.2016.758View
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