Studies on the enantioselectivity of the transesterification of 2-methyl-1,4-butanediol and its derivatives catalyzed by Pseudomonas fluorescens lipase in organic solvents

DOI: 10.1016/S0957-4166(00)80144-5

Source and publish data:

Tetrahedron Asymmetry p. 997 - 1006 (1993)

Update date:2022-08-05

Topics:

Authors:

Grisenti

Ferraboschi

Casati Casati

Santaniello

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Article abstract of DOI:10.1016/S0957-4166(00)80144-5

The irreversible transesterification of 2-methy-1,4-butanediol 1a and its benzyl ethers 2a and 3a catalyzed by Pseudomonas fluorescens lipase in chloroform was studied, the highest ee (> 98%) having been obtained for the 4-benzyl ether 2a.

Full text of DOI:10.1016/S0957-4166(00)80144-5

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Product name:2-Butenoic acid, 3-methyl-4-(phenylmethoxy)-, ethyl ester, (Z)-

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