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- W2117506996 abstract "The enol 2, produced by a Norrish type II photoelimination from 1, is protonated enantioselectively to ketone 3 in the presence of (–)-ephedrine. Best optical yields are obtained at 0oC using small amounts of the chiral aminoalcohol. There is still wide scope for optimization." @default.
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- W2117506996 date "1991-04-01" @default.
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- W2117506996 title "Enantioselective Protonation of a Simple Enol: Aminoalcohol-Catalyzed Ketonization of a Photochemically Produced 2-Methylinden-3-ol" @default.
- W2117506996 doi "https://doi.org/10.1002/anie.199104161" @default.
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