Increased enantioselectivity of lipase in the transesterification ofdl-(±)-3-phenyllactic acid in ionic liquids
Authors:
- Linga BanothLBLinga Banoth
- Manpreet SinghMSManpreet Singh
- Alemu TekeweATAlemu Tekewe
- Uttam BanerjeeUBUttam Banerjee
- 1 July 2009
- journal article
- Published by Taylor & Francis in Biocatalysis and Biotransformation
- Vol. 27 (4) , 263-270
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Esterification of (RS)-Ibuprofen by native and commercial lipases in a two-phase system containing ionic liquidsTetrahedron: Asymmetry, 2006
- Synthesis and anthelmintic activity of substituted (R)-phenyllactic acid containing cyclohexadepsipeptidesBioorganic & Medicinal Chemistry Letters, 2006
- Lipase-Catalyzed Glucose Fatty Acid Ester Synthesis in Ionic LiquidsOrganic Letters, 2005
- The use of lipases immobilized on poly(ethylene oxide) for the preparation of alkyl estersProcess Biochemistry, 2005
- Ionic liquid-phase asymmetric catalytic hydrogenation: hydrogen concentration effects on enantioselectivityTetrahedron: Asymmetry, 2001
- Improving enzymes by using them in organic solventsNature, 2001
- Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosaTetrahedron, 1999
- Chemistry of the mycalamides: antiviral and antitumour compounds from a New Zealand marine sponge. Part 6.1–3 The synthesis and testing of analogues of the C(7)–C(10) fragmentJournal of the Chemical Society, Perkin Transactions 1, 1997
- Lipase catalyzed synthesis of peroxycarboxylic acids and lipase mediated oxidations.Tetrahedron, 1992
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982