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- W2952204699 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." @default.
- W2952204699 created "2019-06-27" @default.
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- W2952204699 date "2008-08-26" @default.
- W2952204699 modified "2023-09-25" @default.
- W2952204699 title "ChemInform Abstract: One-Pot Enol Silane Formation-Mukaiyama Aldol-Type Addition to Dimethyl Acetals Mediated by TMSOTf." @default.
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- W2952204699 doi "https://doi.org/10.1002/chin.200835039" @default.
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