Enantioselective hydrolysis of racemic naproxen methyl ester by two-step acetone-treated Candida rugosa lipase
- 30 November 2001
- journal article
- Published by Elsevier in Process Biochemistry
- Vol. 37 (3) , 293-298
- https://doi.org/10.1016/s0032-9592(01)00213-8
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Candida rugosa lipases: Molecular biology and versatility in biotechnologyYeast, 1998
- Surfactant effect on enhancing (S)-naproxen prodrug production from racemic naproxen by lipaseApplied Biochemistry and Biotechnology, 1997
- A facile enzymatic process for the preparation of (s)-Naproxen ester prodrug in organic solventsEnzyme and Microbial Technology, 1997
- ‘Interfacial activation’ of lipases: facts and artifactsTrends in Biotechnology, 1997
- Lipase-catalyzed esterification in organic solvent to resolve racemic naproxenBiotechnology Letters, 1997
- Chirality and Nonsteroidal Anti-Inflammatory DrugsDrugs, 1996
- Enantioselective esterification of racemic naproxen by lipases in organic solventEnzyme and Microbial Technology, 1994
- Enzymatic resolution of (S)‐(+)‐naproxen in a continuous reactorBiotechnology & Bioengineering, 1991
- A stereoconvergent strategy for the synthesis of enantiomerically pure (R)-(−) and (S)-(+)-2-(6-methoxy-2-naphthyl)-propanoic acid (naproxen)Tetrahedron, 1989
- Nonsteroidal antiinflammatory agents. I. 6-Substituted 2-naphthylacetic acidsJournal of Medicinal Chemistry, 1970