Resolution of isopropylidene-glycerol benzoate by sequential enzymatic hydrolysis and preferential crystallization

DOI: 10.1016/S0957-4166(97)00023-2

Source and publish data:

Tetrahedron Asymmetry p. 817 - 819 (1997)

Update date:2022-08-10

Topics:

Authors:

Bianchi, Daniele

Bosetti, Aldo

Golini, Paolo

Cesti, Pietro

Pina, Carlo

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Article abstract of DOI:10.1016/S0957-4166(97)00023-2

Both enantiomers of isopropylidene-glycerol are prepared from its benzoate ester with enantiomeric excess ≤95% by combined partially stereoselective lipase-catalyzed hydrolysis and preferential crystallization.

Full text of DOI:10.1016/S0957-4166(97)00023-2

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Product name:1,3-Dioxolane-4-methanol, 2,2-dimethyl-, benzoate, (S)-

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