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Issue 6, 2017
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Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry

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Abstract

A new method of azide–alkyne cycloaddition (AAC) in the presence of Zn(OAc)2 as an inexpensive and environmentally friendly catalyst in neat water has been developed. The proposed methodology has been applied for the synthesis of 1,4-disubstituted-1,2,3-triazoles from terminal alkynes and 1,4,5-trisubstituted-1,2,3-triazoles from internal alkynes. It has been found that Zn-catalyzed AAC is extremely sensitive to steric hindrance in acetylenes and a method of regioselective triazole ring formation has been proposed. Particularly important is the isolation and characterization of a relatively stable Zn-containing intermediate, which has been characterized by NMR and HRMS.

Graphical abstract: Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry

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Publication details

The article was received on 06 Dec 2016, accepted on 08 Feb 2017 and first published on 08 Feb 2017


Article type: Research Article
DOI: 10.1039/C6QO00787B
Citation: Org. Chem. Front., 2017,4, 978-985
  • Open access: Creative Commons BY license
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    Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry

    M. A. Morozova, M. S. Yusubov, B. Kratochvil, V. Eigner, A. A. Bondarev, A. Yoshimura, A. Saito, V. V. Zhdankin, M. E. Trusova and P. S. Postnikov, Org. Chem. Front., 2017, 4, 978
    DOI: 10.1039/C6QO00787B

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