Page 107 - Cascade_Biocatalysis_Integrating_Stereoselective_and_Environmentally_Friendly_Reactions

References 83

have already been developed, further biocatalytical extensions are expected in the
coming years exploiting the intrinsic compatibility of enzymes.

References
1. (a) Bartoszewics, A., Ahlsten, N., and 111, 3998–4035; (b) Ghanem, A.
Mart ´ ın-Matute, B. (2013) Chem. Eur. (2007) Tetrahedron, 63, 1721–1754; (c)
J. doi: 10.1002/chem.201202836; (b) Bornscheuer, U.T. and Kazlauskas, R.J.
Kroutil, W., Fischereder, E.-M., Fuchs, (2006) Hydrolases in Organic Synthesis:
C.S., Lechner, H., Mutti, F.G., Pressnitz, Regio and Stereoselective Biotransfor-
D., Rajagopalan, A., Sattler, J.H., Simon, mations, 2nd edn, Wiley-VCH Verlag
R.C., and Siirola, E. (2013) Org. Pro- GmbH, Weinheim.
cess Res. Dev. doi: 10.1021/op4000237; 6. (a) Li, T., Liang, J., Ambrogelly, A.,
(c)Nugent, T.C. (ed) (2010) Chiral Brennan, T., Gloor, G., Huisman, G.,
Amine Synthesis, Wiley-VCH Verlag Lalonde, J., Lekhal, A., Mijts, B., Muley,
GmbH, Weinheim; (d) Nugent, T.C. S., Newman, L., Tobin, M., Wong, G.,
and El-Shazly, M. (2010) Adv. Synth. Zaks, A., and Zhang, X. (2012) J. Am.
Catal., 352, 753–819; (e) H¨ ohne, M. and Chem. Soc., 134, 6467–6472; (b) Turner,
Bornscheuer, U.T. (2009) ChemCatChem, N.J. (2011) Chem. Rev., 111, 4073–4087;
1, 42–51. (c) K¨ ohler, V., Bailey, K.R., Znabet, A.,
2. Noyori, R. (2009) Nat. Chem., 1,5–6. Raftery, J., Helliwell, M., and Turner,
3. For general readings on biocatalysis, N.J. (2010) Angew. Chem. Int. Ed., 49,
see:(a) Faber, K. (2011) Biotransforma- 2182–2184; (d) Dunsmore, C.J., Carr, R.,
tions in Organic Chemistry, 7th edn, Fleming, T., and Turner, N.J. (2006) J.
Springer-Verlag, Berlin; (b) Grunwald, Am. Chem. Soc., 128, 2224–2226.
P. (2009) Biocatalysis: Biochemical Fun- 7. Selected examples: (a) Biava, H. and
damentals and Applications, Imperial Budisa, N. (2013) Tetrahedron Lett. doi:
College Press, London; (c)Fessner, http://dx.doi.org/10.1016/j.tetlet.2013.04.
W.-D. and Anthonsen, T. (eds) (2009) 128 (b) Resch, V., Fabian, W.M., and
Modern Biocatalysis, Wiley-VCH Ver- Kroutil, W. (2010) Adv. Synth. Catal.,
lag GmbH, Weinheim; (d)Gotor, V., 352, 993–997; (c) Kato, D.-I., Miyamoto,
Alfonso, I., and Garcia-Uridales, E. (eds) K., and Ohta, H. (2005) Biocatal. Bio-
(2008) Asymmetric Organic Synthesis with transform., 23, 375–379; (d) Muramatsu,
Enzymes, Wiley-VCH Verlag GmbH, H., Mihara, H., Kakutani, R., Yasuda,
Weinheim; (e) Bommarius, A.S. and M., Ueda, M., Kurihara, T., and Esaki,
Riebel-Bommarius, B.R. (2004) Bio- N. (2004) Tetrahedron: Asymmetry, 15,
catalysis, Wiley-VCH Verlag GmbH, 2841–2843; (e) Sch¨ utte, H., Hummel,
Weinheim. W., Tsai, H., and Kula, M.-R. (1985)
4. (a) Simon, R.C., Mutti, F.G., and Appl. Microbiol. Biotechnol., 22, 306–317.
Kroutil, W. (2013) Drug Discovery Today 8. (a) Abrahamson, M.J., Wong, J.W.,
Technol., 10, 37–44; (b) Mu˜ noz Solano, and Bommarius, A. (2013) Adv. Synth.
D., Hoyos, P., Hern´ aiz, M.J., Alc´ antara, Catal. doi: 10.1002/adsc.201201030 (b)
A.R., and S´ anchez-Montero, J.M. (2012) Abrahamson, M.J., V´ azquez-Figueroa,
Bioresour. Technol., 115, 196–207; E., Woodall, N.B., Moore, J.F., and
(c) Patel, R.N. (2011) ACS Catal., 1, Bommarius, A.S. (2012) Angew.
1056–1074; (d) Patel, R.N. (2008) Coord. Chem.Int.Ed., 51, 3969–3972; (c)
Chem. Rev., 252, 659–701; (e)Patel, R.N. Vaijayanthi, T. and Chadha, A.
(ed) (2006) Biocatalysis in the Pharmaceu- (2008) Tetrahedron: Asymmetry, 19,
tical and Biotechnology Industries,CRC 93–96; (d) Li, H., Williams, P.,
Press, Boca Raton, FL. Micklefield, J., Gardiner, J.M., and
5. (a) Busto, E., Gotor-Fern´ andez, V., Stephens, G. (2004) Tetrahedron,
and Gotor, V. (2011) Chem. Rev., 60, 753–758; (e) Itoh, N., Yachi, C.,