@article {Forro:2012:0929-8673:6178,
title = "Recent Lipase-Catalyzed Hydrolytic Approaches to Pharmacologically Important -and -Amino Acids",
journal = "Current Medicinal Chemistry",
parent_itemid = "infobike://ben/cmc",
publishercode ="ben",
year = "2012",
volume = "19",
number = "36",
publication date ="2012-12-01T00:00:00",
pages = "6178-6187",
itemtype = "ARTICLE",
issn = "0929-8673",
url = "https://www.ingentaconnect.com/content/ben/cmc/2012/00000019/00000036/art00010",
doi = "doi:10.2174/092986712804485683",
keyword = "GC enantioseparation, organic solvent, β-lactam, kinetic resolution, lipase, solvent-free system, candida antarctica lipase B, γ-lactam, β-amino ester, burkholderia cepacia lipase PS, γ-amino acid, enantiomer, β-amino acid, sequential resolution, enzymatic catalysis, supercritical CO2",
author = "Forro, E. and Fulop, F.",
abstract = "Kinetic and sequential kinetic enzymatic routes for the synthesis of enantiomeric - and -amino acids through enzymatic ring cleavage of the corresponding lactams in organic solvents or solvent-free systems or a supercritical CO2 medium, and for the enantioselective hydrolysis
of the corresponding amino esters in organic solvents are reviewed. In the frame of a practical guide, a simple and rapid GC enantioseparation technique for amino acids, including exact descriptions of selected enzymatic reactions, is additionally presented.",
}