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- W1994788648 abstract "The PLE/MPEG catalyzed transesterification of the glycerol ketals rac-1a and rac-1d–f with vinyl propionate in toluene proceeded with good selectivities (E=24–34) and gave the enantiomerically enriched S-alcohols 1a and 1d–f, and the S-esters 2a and 2d–f. High selectivities (E=99 and E≥200) were observed in the transesterification of the glycerol ether rac-3 and its desoxy analog rac-5, both having a secondary hydroxy group, with PLE/MPEG. In transesterifications in organic media PLE exhibited a much higher enantioselectivity than in hydrolysis in water." @default.
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- W1994788648 date "1999-09-01" @default.
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- W1994788648 title "Application of pig liver esterase catalyzed transesterification in organic media to the kinetic resolution of glycerol derivatives" @default.
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