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

Volume: 19, Issue: 2, Pages: 654 - 664
Published: Nov 13, 2012
Abstract
With the use of benzonitrile‐stabilized Au I catalyst [Au(IPr)(NCPh)]SbF 6 ( 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...
Paper Details
Title
Gold(I)‐Catalyzed Divergence in the Preparation of Bicyclic Enol Esters: From Exclusively [3C+2C]‐Cycloaddition Reactions to Exclusive Formation of Vinylcyclopropanes
Published Date
Nov 13, 2012
Volume
19
Issue
2
Pages
654 - 664
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