Direct asymmetric aldol addition of an α-CF amide to arylglyoxal hydrates was promoted by a chiral catalyst comprising a soft Lewis acidic Cu(I), a chiral bisphosphine ligand, and DBU. The 7-azaindoline moiety of the amide facilitates its enolization and stabilizes the thus-generated Cu enolate, furnishing enantioenriched aldol adducts.
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http://dx.doi.org/10.1021/acs.joc.7b01381 | DOI Listing |
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