Enantiomers of Ring-Substituted 2-Amino-1-phenylethanols by Pseudomonas cepacia Lipase

DOI: 10.1016/0957-4166(95)00303-7

Source and publish data:

Tetrahedron Asymmetry p. 2281 - 2286 (1995)

Update date:2022-08-04

Topics:

Authors:

Lundell, Katri

Kanerva, Liisa T.

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Article abstract of DOI:10.1016/0957-4166(95)00303-7

The enantiomers of 2-amino-1-phenylethanols were obtained enantiomerically pure (ee > 95percent) at 50percent conversion by the Pseudomonas cepacia lipase-catalysed O-acylation of amino alcohols or O-deacylation of the corresponding N,O-diacylated compoun

Full text of DOI:10.1016/0957-4166(95)00303-7

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