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Gold(I)-Catalyzed Divergence in the Preparation of Bicyclic Enol Esters: From Exclusively [3C+2C]-Cycloaddition Reactions to Exclusive Formation of Vinylcyclopropanes

Authors

  • Ryan C. Conyers,

    1. Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 (USA), Fax: (+1) 513-529-5715
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  • Prof. Dr. Benjamin W. Gung

    Corresponding author
    1. Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 (USA), Fax: (+1) 513-529-5715
    • Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 (USA), Fax: (+1) 513-529-5715
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Abstract

With the use of benzonitrile-stabilized AuI catalyst [Au(IPr)(NCPh)]SbF6 (Ic; IPr=1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene), a spectrum of reactivity is observed for propargyl ester 4 a with cyclic vinyl ethers, ranging from exclusively [3C+2C] cycloaddition reactions to exclusively cyclopropanation depending only on the structure of the substrate. Some initially formed cyclopropanation products rearrange into the corresponding formally [3C+2C] cycloaddition products after treatment with fresh AuI complex at 80 °C. Vinylcyclopropanes formed from dihydrofuran and dihydropyran resisted such rearrangement, even in the presence of fresh AuI catalyst at elevated temperature. This study addresses an important mechanistic question concerning whether the five-membered-ring products were produced by a direct [3C+2C] cycloaddition reaction or by a sequential cyclopropanation/ring-expansion reaction. A dual pathway is proposed for the AuI-catalyzed reactions between propargyl esters and cyclic vinyl ethers. The different behavior among vinyl cyclic ethers is attributed to the difference in the polarization of the π bond. Highly polarized bonds appear to undergo the cycloaddition reaction whereas less polar π-bonds produce cyclopropanes.

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