SEARCH

SEARCH BY CITATION

References

  • Arnold, F.H., and Georgiou, G. (2003) Directed Evolution Library Creation. Totowa, NJ, USA: Humana Press.
  • Baumann, M., Hauer, B.H., and Bornscheuer, U.T. (2000) Rapid screening of hydrolases for the enantioselective conversion of ‘difficult-to-resolve’ substrates. Tetrahedron: Asymmetry 11: 47814790.
  • Bornscheuer, U.T. (2002) Methods to increase enantioselectivity of lipases and esterases. Curr Opin Biotechnol 13: 543547.
  • Bornscheuer, U.T., and Kazlauskas, R.J. (2006) Hydrolases in Organic Synthesis. Weinheim, Germany: Wiley-VCH.
  • Brüsehaber, E., Böttcher, D., Liebeton, K., Eck, J., Naumer, C., and Bornscheuer, U.T. (2008) Asymmetric synthesis of cis-3,5-diacetoxycyclopent-1-ene using metagenome-derived hydrolases. Tetrahedron: Asymmetry 19: 730732.
  • Chavda, S., Coumbarides, G.S., Dingjan, M., Eames, J., Flinn, A., Ghilagaber, S., et al. (2007) Synthesis of enantiomerically pure isotopomers of 2-phenylpropionic acids. Chirality 19: 366373.
  • Chen, C.S., Fujimoto, Y., Girdaukas, G., and Sih, C.J. (1982) Quantitative analyses of biochemical kinetic resolutions of enantiomers. J Am Chem Soc 104: 72947299.
  • Elend, C., Schmeisser, C., Leggewie, C., Babiak, P., Carballeira, J.D., Steele, H.L., et al. (2006) Isolation and biochemical characterization of two novel metagenome-derived esterases. Appl Environ Microbiol 72: 36373645.
  • Faber, K. (2004) Biotransformations in Organic Chemistry. Berlin, Germany: Springer Verlag.
  • Fuganti, C., and Serra, S. (2000) Baker's yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (−)-curcuquinone and (+)-curcuhydroquinone. J Chem Soc, Perkin Trans 1: 37583764.
  • Fuganti, C., Serra, S., and Dulio, A. (1999) Baker's yeast mediated enantioselective synthesis of the bisabolane sesquiterpenes curcumene, turmerone, dehydrocurcumene and nuciferal. J Chem Soc, Perkin Trans 1: 279282.
  • Gabor, E., Liebeton, K., Nielhaus, F., Eck, J., and Lorenz, P. (2007) Updating the metagenomics toolbox. Biotechnol J 2: 201206.
  • Hashimoto, N., Aoyama, T., and Shioiri, T. (1981) New methods and reagents in organic-synthesis. 14. A simple efficient preparation of methyl esters with trimethylsilyldiazomethane (TMSCHN2) and its application to gas chromatographic analysis of fatty acids. Chem Pharm Bull 29: 14751478.
  • Henke, E., Pleiss, J., and Bornscheuer, U.T. (2002) Activity of lipases and esterases towards tertiary alcohols: insights into structure-function relationships. Angew Chem Int Ed Engl 41: 32113213.
  • Kamal, A., Malik, M.S., Shaik, A.A., and Azeeza, S. (2007) Enantioselective synthesis of (R)- and (S)-curcumene and curcuphenol: an efficient chemoenzymatic route. Tetrahedron: Asymmetry 18: 25472553.
  • Kogure, T., and Eliel, E.L. (1984) A convergent asymmetric synthesis of (−)-malyngolide and its three stereoisomers. J Org Chem 49: 576578.
  • Kourist, R., Krishna, S.H., Patel, J.S., Bartnek, F., Hitchman, T.S., Weiner, D.P., and Bornscheuer, U.T. (2007) Identification of a metagenome-derived esterase with high enantioselectivity in the kinetic resolution of arylaliphatic tertiary alcohols. Org Biomol Chem 5: 33103313.
  • Kourist, R., Nguyen, G.S., Strübing, D., Böttcher, D., Liebeton, K., Naumer, C., et al. (2008) Hydrolase-catalyzed stereoselective preparation of protected α, α-dialkyl-α-hydroxycarboxylic acids. Tetrahedron: Asymmetry 19: 18391943.
  • Lorenz, P., and Eck, J. (2005) Metagenomics and industrial applications. Nat Rev Microbiol 3: 510516.
  • Lorenz, P., Liebeton, K., Niehaus, F., Schleper, C., and Eck, J. (2003) The impact of non-cultivated biodiversity on enzyme discovery and evolution. Biocatal Biotransform 21: 8791.
  • Mori, K. (2005) Synthesis of (R)-ar-turmerone and its conversion to (R)-ar-himachalene, a pheromone component of the flea beetle: (R)-ar-himachalene is dextrorotatory in hexane, while levorotatory in chloroform. Tetrahedron: Asymmetry 16: 17211721.
  • Noorduin, W.L., Kaptein, B., Meekes, H., Van Enckevort, W.J., Kellogg, R.M., and Vlieg, E. (2009) Fast attrition-enhanced deracemization of naproxen by a gradual in situ feed. Angew Chem Int Ed Engl 48: 45814583.
  • Ollis, D.L., Cheah, E., Cygler, M.E., Eckstein, E., Dijkstra, B.W., Frolow, F., et al. (1992) The alpha/beta hydrolase fold. Protein Eng 5: 197211.
  • Piccolo, O., Azzena, U., Melloni, G., Delogu, G., and Valoti, E. (1991) Stereospecific Friedel-Crafts alkylation of aromatic compounds: synthesis of optically active 2-and 3-arylalkanoic esters. J Org Chem 56: 183187.
  • Schmeisser, C., Stockigt, C., Raasch, C., Wingender, J., Timmis, K.N., Wenderoth, D.F., et al. (2003) Metagenome survey of biofilms in drinking-water networks. Appl Environ Microbiol 69: 72987309.
  • Sonawane, H.R., Bellur, N.S., Ahuja, J.R., and Kulkarni, D.G. (1992) Recent developments in the synthesis of optically active alpha-arylpropanoic acids – an important class of nonsteroidal antiinflammatory agents. Tetrahedron: Asymmetry 3: 163192.
  • Steele, H.L., Jaeger, K.E., Daniel, R., and Streit, W.R. (2009) Advances in recovery of novel biocatalysts from metagenomes. J Mol Microbiol Biotechnol 16: 2537.
  • Stephan, E., Rocher, R., Aubouet, J., Pourcelot, G., and Cresson, P. (1994) Preparation of chiral indanones and dihydrocoumarins – application to synthesis of (+)-3-(2,6-dimethoxyphenyl) pentanoic acid. Tetrahedron: Asymmetry 5: 4144.
  • Sun, X.F., Zhou, L., Wang, C.J., and Zhang, X.M. (2007) Rh-catalyzed highly enantioselective synthesis of 3-arylbutanoic acids. Angew Chem Int Ed Engl 46: 26232626.
  • Um, P.J., and Drueckhammer, D.G. (1998) Dynamic enzymatic resolution of thioesters. J Am Chem Soc 120: 56055610.
  • Varadharaj, G., Hazell, K., and Reeve, C.D. (1998) An efficient preparative scale resolution of 3-phenylbutyric acid by lipase from Burkholderia cepacia (Chirazyme L1). Tetrahedron: Asymmetry 9: 11911195.
  • Yang, H., Henke, E., and Bornscheuer, U.T. (1999) The use of vinyl esters significantly enhanced enantioselectivities and reaction rates in lipase-catalyzed resolutions of arylaliphatic carboxylic acids. J Org Chem 64: 17091712.