Synthesis 2012; 44(24): 3722-3730
DOI: 10.1055/s-0032-1317697
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© Georg Thieme Verlag Stuttgart · New York

Copper on Iron: Catalyst and Scavenger for Azide–Alkyne Cycloaddition

Authors

  • Szabolcs Kovács

    a   Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny. 1/a, Budapest 1117, Hungary
  • Katalin Zih-Perényi

    a   Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny. 1/a, Budapest 1117, Hungary
  • Ádám Révész

    b   Department of Materials Physics, Institute of Physics, Eötvös Loránd University, Pázmány Péter stny. 1/a, Budapest 1117, Hungary    Fax: +36(1)3722909   eMail: novakz@elte.hu
  • Zoltán Novák*

    a   Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny. 1/a, Budapest 1117, Hungary
Weitere Informationen

Publikationsverlauf

Received: 14. September 2012

Accepted after revision: 31. Oktober 2012

Publikationsdatum:
20. November 2012 (online)


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Abstract

Dipolar cycloaddition of terminal alkynes and azides catalyzed by the Cu/Fe bimetallic system is reported. In the presence of a readily accessible nanosized copper source, the cycloaddition reaction can be easily achieved at ambient temperature with high efficiency. The product obtained from the reaction catalyzed by Cu/Fe contains significantly lower copper contaminants compared to various active homogeneous copper complexes. Iron not only behaves as support for copper, but acts as a redox scavenger, and reduces the copper contamination of the organic product.

Supporting Information