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Synfacts 2006(7): 0673-0673
DOI: 10.1055/s-2006-941874
DOI: 10.1055/s-2006-941874
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart · New York
RCM Helicene Synthesis
S. K. Collins*, A. Grandbois, M. P. Vachon, J. Côté
Université de Montréal, Canada
Further Information
Publication History
Publication Date:
22 June 2006 (online)
Significance
A new procedure for the synthesis of helicenes by ring-closing metathesis of olefin-functionalized binaphthols is reported. Two different sets of conditions were explored. The first utilizes Grubbs 2nd generation catalyst (1) with microwave heating for 25-120 min. The second uses catalyst 2 with conventional heating at 40 °C for 24 h. These conditions were tested on a variety of substituted binaphthols with isolated yields ranging from 22-93%. In all instances, with the exception of the parent compound, the microwave conditions provided superior yields.