Pharmaceuticals through enzymatic transesterification and enzymatic aminolysis reactions

Authors
Citation
V. Gotor, Pharmaceuticals through enzymatic transesterification and enzymatic aminolysis reactions, BIOCATAL B, 18(2), 2000, pp. 87-103
Citations number
41
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCATALYSIS AND BIOTRANSFORMATION
ISSN journal
10242422 → ACNP
Volume
18
Issue
2
Year of publication
2000
Pages
87 - 103
Database
ISI
SICI code
1024-2422(2000)18:2<87:PTETAE>2.0.ZU;2-S
Abstract
Biotransformations are now accepted as a methodology for the preparation of fine chemicals. The majority of enzyme-catalysed reactions involve the use of hydrolases, especially lipases, in hydrolysis or transesterification re actions. Over the last few years, other interesting processes have appeared , not only with hydrolases but also with oxidoreductases and oxynitrilases. However, the use of lipases in organic solvents proves an excellent method ology for the preparation of single-isomer chiral drugs by enzymatic transe sterification and aminolysis reaction.