Journal article

Authors list: Auzias, MG; Neuburger, M; Wegner, HA

Publication year: 2010

Pages: 2443-2448

Journal: Accounts and Rapid Communications in Chemical Synthesis

Volume number: 2010

Issue number: 16

ISSN: 0936-5214

DOI Link: https://doi.org/10.1055/s-0030-1258566

Publisher: Thieme

Abstract: 
A new heterogeneous gold-catalyzed system for the domino cyclization oxidative coupling of 2-alkynyl phenols for the formation of 3,3'-bisbenzofurans was developed. The substrate and the catalyst scope as well as the reaction conditions were investigated and optimized. This method provides access to this novel structural theme in two steps starting from commercially available chemicals. The molecular structure of the 3,3'-bisbenzofurans was confirmed by single-crystal X-ray analysis.

Harvard Citation style: Auzias, M., Neuburger, M. and Wegner, H. (2010) 3,3 '-Bis(arylbenzofurans) via a Gold-Catalyzed Domino Process, Accounts and Rapid Communications in Chemical Synthesis, 2010(16), pp. 2443-2448. https://doi.org/10.1055/s-0030-1258566

APA Citation style: Auzias, M., Neuburger, M., & Wegner, H. (2010). 3,3 '-Bis(arylbenzofurans) via a Gold-Catalyzed Domino Process. Accounts and Rapid Communications in Chemical Synthesis. 2010(16), 2443-2448. https://doi.org/10.1055/s-0030-1258566