Gold-catalyzed diastereoselective [2+2+2]-cycloaddition of 1,7-enynes with carbonyl compounds

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Abstract

We report a gold-catalyzed [2+2+2]-cycloaddition of 1,7-enynes with carbonyl species; our experimental data suggest that the resulting oxacyclic cycloadducts arose from an interception of gold-containing cyclobutenium intermediates with carbonyl species. © 2012 The Royal Society of Chemistry.

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Huple, D. B., & Liu, R. S. (2012). Gold-catalyzed diastereoselective [2+2+2]-cycloaddition of 1,7-enynes with carbonyl compounds. Chemical Communications, 48(89), 10975–10977. https://doi.org/10.1039/c2cc36219h

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