Catalysis Science & Technology
Paper
11 F. Vertregt, G. Torrelo, S. Trunk, H. Wiltsche, W. R.
Hagen, U. Hanefeld and K. Steiner, ACS Catal., 2016, 6,
5081–5085.
12 U. Hanefeld, Chem. Soc. Rev., 2013, 42, 6308–6321.
13 M. Hartmann and X. Kostrov, Chem. Soc. Rev., 2013, 42,
6277–6289.
14 K. Zielinska, K. Szymanska, R. Mazurkiewicz and A.
Jarzebski, Tetrahedron: Asymmetry, 2017, 28, 146–152.
15 P. Bracco, G. Torrelo, S. Noordam, G. de Jong and U.
Hanefeld, Catalysts, 2018, 8, 287.
29 M. Bajić, I. Plazl, R. Stloukal and P. Žnidaršič-Plazl, Process
Biochem., 2017, 52, 63–72.
30 M. Planchestainer, M. L. Contente, J. Cassidy, F. Molinari, L.
Tamborini and F. Paradisi, Green Chem., 2017, 19, 372–375.
31 C. Zor, H. A. Reeve, J. Quinson, L. A. Thompson, T. H.
Lonsdale, F. Dillon, N. Grobert and K. A. Vincent, Chem.
Commun., 2017, 53, 9839–9841.
32 F. Dall'Oglio, M. L. Contente, P. Conti, F. Molinari, D.
Monfredi, A. Pinto, D. Romano, D. Ubiali, L. Tamborini and
I. Serra, Catal. Commun., 2017, 93, 29–32.
16 D. Okrob, M. Paravidino, R. V. A. Orru, W. Wiechert, U.
Hanefeld and M. Pohl, Adv. Synth. Catal., 2011, 353,
2399–2408.
33 V. De Vitis, F. Dall'Oglio, A. Pinto, C. De Micheli, F. Molinari,
P. Conti, D. Romano and L. Tamborini, ChemistryOpen,
2017, 6, 668–673.
17 E. Wehtje, P. Adlercreutz and B. Mattiasson, Biotechnol.
Bioeng., 1990, 36, 39–46.
34 H. Lamble, S. F. Royer, D. W. Hough, M. J. Danson, G. L.
Taylor and S. D. Bull, Adv. Synth. Catal., 2007, 349, 817–821.
35 B. Grabner, Y. Pokhilchuk and H. Gruber-Woelfler, Catalysts,
2020, 10, 137.
36 U. Hanefeld, A. J. J. Straathof and J. J. Heijnen, Biochim.
Biophys. Acta, 1999, 1432, 185–193.
37 L. van Langen, F. van Rantwijk and R. A. Sheldon, Org.
Process Res. Dev., 2003, 7, 828–831.
38 U. Hanefeld, L. Gardossi and E. Magner, Chem. Soc. Rev.,
2009, 38, 453–468.
18 R. Lindeque and J. Woodley, Catalysts, 2019, 9, 262.
19 H. Larsson, P. A. Schjøtt, E. Byströ, K. V. Gernaey and U.
Krühne, Ind. Eng. Chem. Res., 2017, 56, 3853–3865.
20 H. Mallin, J. Muschiol, E. Byström and U. Bornscheuer,
ChemCatChem, 2013, 5, 3529–3532.
21 M. P. van der Helm, P. Bracco, H. Busch, K. Szymańska, A.
Jarzębski and U. Hanefeld, Catal. Sci. Technol., 2019, 9,
1189–1200.
22 R. Munirathinam, J. Huskens and W. Verboom, Adv. Synth.
Catal., 2015, 357, 1093–1123.
39 F. Effenberger, J. Eichhorn and J. Roos, Tetrahedron:
Asymmetry, 1995, 6, 271–282.
23 N. N. Rao, S. Lütz, K. Würges and D. Minör, Org. Process Res.
Dev., 2009, 13, 607–616.
40 D. Costes, E. Wehtje and P. Adlercreutz, Enzyme Microb.
Technol., 1999, 25, 384–391.
24 K. G. Hugentobler, M. Rasparini, L. A. Thompson, K. E.
Jolley, A. J. Blacker and N. J. Turner, Org. Process Res. Dev.,
2017, 21, 195–199.
25 A. Brahma, B. Musio, U. Ismayilova, N. Nikbin, S.
Kamptmann, P. Siegert, G. E. Jeromin, S. V. Ley and M. Pohl,
Synlett, 2016, 27, 262–266.
41 A. Basso, L. De Martin, C. Ebert, L. Gardossi and P. Linda,
J. Mol. Catal. B: Enzym., 2000, 8, 245–253.
42 K. Szymanska, K. Odrozek, A. Zniszczoł, W. Pudło and A. B.
Jarzebski, Chem. Eng. J., 2017, 315, 18–24.
43 S. E. Charma and B. L. Wong, Enzyme Microb. Technol.,
1981, 3, 111–118.
26 L. van den Biggelaar, P. Soumillion and D. P. Debecker,
Catalysts, 2017, 7, 54.
44 A. H. M. M. El-Sayed, W. M. Mahmoud and R. W. Coughlin,
Biotechnol. Bioeng., 1990, 36, 83–91.
27 M. Movsisyan, E. I. P. Delbeke, J. K. E. T. Berton, C.
Battilocchio, S. V. Ley and C. V. Stevens, Chem. Soc. Rev.,
2016, 45, 4892–4928.
28 L. H. Andrade, W. Kroutil and T. F. Jamison, Org. Lett.,
2014, 16, 6092–6095.
45 N. J. Gleason and J. D. Carbeck, Langmuir, 2004, 20, 6374–6381.
46 T. R. Besanger, R. J. Hodgson, J. R. A. Green and J. D.
Brennan, Anal. Chim. Acta, 2006, 564, 106–115.
47 Y. Zhu, Q. Chen, L. Shao, Y. Jiacef and X. Zhang, React.
Chem. Eng., 2020, 5, 9–32.
This journal is © The Royal Society of Chemistry 2020
Catal. Sci. Technol.