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- W2115922204 abstract "O-Allylations and O-benzylations of a-hydroxy esters (3a-3c) are performed without racemization. The reagents applied, O-allyl- and O-benzyltrichloroacetimidate (5a, 5b) are prepared and converted in a one-pot-procedure. After protection by benzylation (S)-(-)-ethyl lactate (3a) is converted by a sequence of carbonyl reduction, alcohol activation, ether formation, and deprotection to the optically active diglycole derivative 1a" @default.
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- W2115922204 date "2000-09-01" @default.
- W2115922204 modified "2023-10-16" @default.
- W2115922204 title "One-Pot Generation and Conversion of Trichloroacetimidates for the Racemization-Free Allylation and Benzylation of α-Hydroxyesters and the Enantiopure Synthesis of a Chiral Diglycole" @default.
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- W2115922204 doi "https://doi.org/10.1002/1521-3897(200009)342:7<654::aid-prac654>3.0.co;2-z" @default.
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