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2000
Volume 17, Issue 1
  • ISSN: 1570-1794
  • E-ISSN: 1875-6271

Abstract

Introduction: An effective Cu-complex, [Cu(NH3)4SO4 • H2O] was prepared conveniently from the inexpensive and easily available starting reagents in a simple route. Materials and Methods: Excellent reactivity of the catalyst was observed towards two competent clickcycloadditions: (a) oxidative cycloaddition of azides with electron-poor olefins and (b) one-pot cycloaddition of alkynes with boronic acid and sodium azide under “click-appropriate” conditions. Results: No external oxidant, short reaction time, high product yield, wide substrate scope, and aqueous solvent media make the azide-olefin cycloaddition approach a greener route in contrast to the reported methods. Conclusion: The newly developed mild, green, and rapid three-component strategy shows product diversity with superb yields at room temperature by reducing the synthetic process time and using only 1 mol % of the synthesized copper complex.

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/content/journals/cos/10.2174/1570179417666191223152643
2020-02-01
2025-05-29
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/content/journals/cos/10.2174/1570179417666191223152643
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  • Article Type:
    Research Article
Keyword(s): 1,2,3-triazole; Ammoniated Cu-complex; aqueous media; boronic acid; OAOC; regioselective
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