References
- AbellAD, BluntJW, FouldsGJ, MunroMHG. 1997. Chemistry of the mycalamides: antiviral and antitumor compounds from a New Zealand amrine sponge. Part 6. The synthesis and testing of the analogues of the C7–C10 fragment. J Chem Soc Perkin Trans 1:1647–1654.
- BergerA, de SouzaRF, DelgadoMR, DupontJ. 2001. Ionic liquid-phase asymmetric catalytic hydrogenation: hydrogen concentration effects on enantioselectivity. Tetrahedron Asymm 12:1825–1828.
- BjörklingF, FrykmanH, GodtfredsenSE, KirkO. 1992. Lipase catalyzed synthesis of peroxycarboxylic acids and lipase mediated oxidations. Tetrahedron 48:4587–4592.
- ChenC-S, FujimotoY, GirdaukasG, SihCJ. 1982. Quantitative analysis of biochemical kinetic resolutions of enantiomers. J Am Chem Soc 104:7294–7299.
- ContesiniFJ, de Oliveira CarvalhoP. 2006. Esterification of (RS)-ibuprofen by native and commercial lipases in a two-phase system containing ionic liquids. Tetrahedron Asymm 17:2069–2073.
- da Silva CrespoJ, QueirozN, da Graca NascimentoM, SoldiV. 2005. The use of lipases immobilized on poly(ethylene oxide) for the preparation of alkyl esters. Process Biochem 40:401–409.
- GanskeF, BornscheuerUT. 2005. Lipase-catalyzed glucose fatty acid ester synthesis in ionic liquids. Org Lett 7:3097–3098.
- IshidaK, OkitaY, MatsudaH, OkinoT, MurakamiM. 1999. Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa. Tetrahedron 55:10971–10988.
- JeschkeP, BuchholzJB, HarderA, EtzelW, SchindlerM, GauW, WeissHC. 2006. Synthesis and anthelmintic activity of substituted (R)-phenyllactic acid containing cyclohexadepsipeptides. Bioorg Med Chem Lett 16:4410–4415.
- KimKW, SongB, ChoiMY, KimM. 2001. Biocatalysis in ionic liquids: markedly enhanced enantioselectivity of lipase. J Org Lett 3:1507–1509.
- KlibanovAM. 2001. Improving enzymes by using them in organic solvents. Nature 409:241–246.
- KraglU, EcksteinM, KaftzikN. 2002. Enzyme catalysis in ionic liquids. Curr Opin Biotechnol 13:565–571.
- LauRM, van-RantwijkF, SeddonKR, SheldonRA. 2000. Lipase-catalyzed reactions in ionic liquids. Org Lett 2:4189–4191.
- LiuBK, WangN, ChenZC, WuQ, LinXF. 2006. Markedly enhancing lipase-catalyzed synthesis of nucleoside drugs’ ester by using a mixture system containing organic solvents and ionic liquid. Bioorg Med Chem Lett 16:3769–3771.
- MengXJ, KabalkaGW. 1998. Enantioselective synthesis of α-hydroxy carboxylic acids: direct conversion of α-oxocarboxylic acids to enantiomerically enriched α-hydroxy carboxylic acids via neighboring group control. Tetrahedron Lett 39:5501–5504.
- MiyazawaT, ImagawaK, YamadaT. 2006. Use of Aspergillus oryzae protease for the resolution of α-hydroxy acids by enantioselective ester hydrolysis. Biocatal Biotransform 24:291–298.
- SchnellBL, SilviaM, GlueckM, KroutilW, FaberK. 2006. Enantio-complementary deracemization of (±)-2-hydroxy-4-phenylbutanoic acid and (±)-3-phenyllactic acid using lipase-catalyzed kinetic resolution combined with biocatalytic racemization. Tetrahedron 62:2912–2916.
- ShahS, GuptaMN. 2007. Kinetic resolution of (±)-1-phenylethanol in [BMIM][PF6] using high activity preparations of lipases. Bioorg Med Chem Lett 17:921–924.
- SharmaR, ChistiY, BanerjeeUC. 2001. Production, purification, characterization, and applications of lipases. Biotechnol Adv 19:627–662.
- SinghS, BanerjeeUC. 2005. Enantioselective hydrolysis of methoxyphenyl glycidic acid methyl ester [(±)-MPGM] by a thermostable and alkalostable lipase from Pseudomonas aeruginosa. J Mol Catal B: Enzym 36:30–35.
- SinghM, BanerjeeUC. 2007. Enantioselective transesterification of (RS)-1-chloro-3-(3,4-difluorophenoxy)-2-propanol using Pseudomonas aeruginosa lipases. Tetrahedron Asymm 18:2079–2085.
- SpindlerF, PittelkowU, BlaserHU. 1991. A highly enantioselective rhodium catalyst for the hydrogenation of the aliphatic α-keto esters. Chirality 3:370–375.
- StrömK, SjögrenJ, BrobergA, SchnürerJ. 2002. Lactobacillus plantarum MiLAB 393 produces the antifungal cyclic dipeptides cyclo(l-Phe-l-Pro) and cyclo(l-Phe-trans-4-OH-l-Pro) and 3-phenyllactic acid. Appl Environ Microbiol 68:4322–4327.
- TekeweA, SinghS, SinghM, MohanU, BanerjeeUC. 2008. Development and validation of HPLC method for the resolution of drug intermediates: dl-3-phenyllactic acid, dl-O-acetyl-3-phenyllactic acid and (±)-mexiletine acetamide enantiomers. Talanta 75:239–245.
- VallsN, VallriberaM, López-CanetM, BonjochJ. 2002. Synthesis of microcin SF608. J Org Chem 67:4945–4950.
- van RantwijkF, Madeira LauR, SheldonRA. 2003. Biocatalytic transformations in ionic liquids. Trends Biotechnol 21:131–138.
- WagnerM. 2005. Biocatalysis in ionic liquids. Chem Today 23:32–34.
- WallertS, DrauzK, GraysonI, GrögerH, MariadPD, BolmC. 2005. Ionic liquids as additives in the pig liver esterase (PLE) catalysed synthesis of chiral disubstituted malonates. Green Chem 7:602–605.
- WinklerUK, StuckmannM. 1979. Glycogen, hyaluronate, and some other polysaccharides greatly enhance the formation of exolipase by Serratia marcescens. J Bacteriol 138:663–670.
- YangZ, PanW. 2005. Ionic liquids: green solvents for nonaqueous biocatalysis. Enzyme Microb Technol 37:19–28.