A Study of Epoxyolefin Cyclizations Catalyzed by Bismuth Trifluoromethanesulfonate and Other Metal Triflates
Epoxyolefin cyclizations have attracted considerable interest due to their importance in biosynthetic pathways. Bismuth trifluoromethanesulfonate as well as several other metal triflates are shown to be highly effective (0.1 mol %) catalysts for the cyclization of geraniolene oxide. The product composition is found to be more dependent on solvent and substrate concentration than on the nature of the metal triflate. Cyclization products are favored in CH2Cl2 and under high dilution conditions. Ether solvents favored acyclic products.
Ram S. Mohan, Joshua R. Lacey, Peter W. Anzalone, Christopher M. Duncan, and Matthew J. Hackert. "A Study of Epoxyolefin Cyclizations Catalyzed by Bismuth Trifluoromethanesulfonate and Other Metal Triflates" Tetrahedron Letters 46 (2005): 8507-8511.
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