Unprecedented alkylation of silyl enol ethers has been developed by the use of ortho-alkynylbenzoic acid alkyl esters as alkylating agents in the presence of a gold catalyst. The reaction probably proceeds through the gold-induced in situ construction of leaving groups and subsequent nucleophilic attack on the silyl enol ethers. The generated leaving compound abstracts a proton to regenerate the silyl enol ether structure.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107469 | PMC |
http://dx.doi.org/10.3762/bjoc.7.76 | DOI Listing |
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