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- W2023676848 abstract "The kinetic resolution of ferrocenyl aldol 2 was achieved by a lipase-catalyzed esterification in organic solvent. Lipase from Candida antarctica was also found effective in promoting the enantioselective alcoholysis of acetate (±)-3 with n-BuOH. Both enantiomers of 2 were obtained in enantiopure form and subjected to chemical reduction to afford the corresponding syn- and anti-diols. These diols serve as starting materials for the preparation of new ferrocenyl amino alcohols bearing two stereocenters in the side chain." @default.
- W2023676848 created "2016-06-24" @default.
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- W2023676848 date "2006-03-01" @default.
- W2023676848 modified "2023-09-23" @default.
- W2023676848 title "Chemoenzymatic access to all four enantiopure stereoisomers of 1-ferrocenyl-1,3-butanediol" @default.
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- W2023676848 doi "https://doi.org/10.1016/j.tetasy.2006.01.028" @default.
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