One-pot enol silane formation-Mukaiyama Aldol-type addition to dimethyl acetals mediated by TMSOTf
CW Downey, MW Johnson…
Index: Downey, C. Wade; Johnson, Miles W.; Tracy, Kathryn J. Journal of Organic Chemistry, 2008 , vol. 73, # 8 p. 3299 - 3302
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Citation Number: 26
Abstract
Various ketones, esters, amides, and thioesters add in high yield to dimethyl acetals in the presence of silyl trifluoromethanesulfonates and an amine base. Acetals derived from aryl, unsaturated, and aliphatic aldehydes are all effective substrates. The reaction proceeds in a single reaction flask, with no purification of the intermediate enol silane necessary.
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