Issue 86, 2014

Raney Ni catalyzed azide-alkyne cycloaddition reaction

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

Supplementary files

Article information

Article type
Communication
Submitted
13 Jul 2014
Accepted
10 Sep 2014
First published
10 Sep 2014

RSC Adv., 2014,4, 46040-46048

Author version available

Raney Ni catalyzed azide-alkyne cycloaddition reaction

H. Surya Prakash Rao and G. Chakibanda, RSC Adv., 2014, 4, 46040 DOI: 10.1039/C4RA07057G

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