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Raney Ni catalyzed azide-alkyne cycloaddition reaction†
H. Surya Prakash Rao,Guravaiah Chakibanda
RSC Advances Pub Date : 09/10/2014 00:00:00 , DOI:10.1039/C4RA07057G
Abstract

Raney Ni efficiently catalyzes acetylene azide cycloaddition reactions to form 1,2,3-triazoles. Unlike the CuSO4/sodium ascorbate reagent system, there is no need for a reducing agent under Raney Ni catalysis. Terminal acetylene selectivity, 1,4-regioselectivity and mild reaction conditions are prominent features of the method. Mechanistic probing revealed that the reaction does not go through nickel acetylides.

Graphical abstract: Raney Ni catalyzed azide-alkyne cycloaddition reaction
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