-
3
-
-
84857235492
-
-
ed. J.-E. Bäckvall, Wiley-VCH, Weinheim, 2nd edn
-
I. W. C. E. Arends and R. A. Sheldon, Modern Oxidation Methods, ed., J.-E. Bäckvall, Wiley-VCH, Weinheim, 2nd edn, 2010, pp. 147-185
-
(2010)
Modern Oxidation Methods
, pp. 147-185
-
-
Arends, I.W.C.E.1
Sheldon, R.A.2
-
4
-
-
84889491633
-
-
ed., Wiley-VCH, Weinheim
-
Modern Biooxidation: Enzymes, Reactions and Applications, ed., R. D. Schmid, and, V. B. Urlacher, Wiley-VCH, Weinheim, 2007
-
(2007)
Modern Biooxidation: Enzymes, Reactions and Applications
-
-
Schmid, R.D.1
Urlacher, V.B.2
-
5
-
-
84888652145
-
-
ed., John Wiley & Sons, Hoboken
-
Redox Biocatalysis: Fundamentals and Applications, ed., D. Gamenara, G. A. Seoane, P. Saenz-Méndez, and, P. Domínguez de María, John Wiley & Sons, Hoboken, 2013
-
(2013)
Redox Biocatalysis: Fundamentals and Applications
-
-
Gamenara, D.1
Seoane, G.A.2
Saenz-Méndez, P.3
Domínguez De María, P.4
-
6
-
-
84887081741
-
-
ed. K. Drauz, H. Gröger and O. May, Wiley-VCH, Weinheim
-
F. Hollmann, K. Bühler and B. Bühler, in Enzyme Catalysis in Organic Synthesis, ed., K. Drauz, H. Gröger, and, O. May, Wiley-VCH, Weinheim, 2012, pp. 1325-1438
-
(2012)
Enzyme Catalysis in Organic Synthesis
, pp. 1325-1438
-
-
Hollmann, F.1
Bühler, K.2
Bühler, B.3
-
17
-
-
34548605576
-
-
M. Zumárraga T. Bulter S. Shleev J. Polaina A. Martínez-Arias F. J. Plou A. Ballesteros M. Alcalde Chem. Biol. 2007 14 1052 1064
-
(2007)
Chem. Biol.
, vol.14
, pp. 1052-1064
-
-
Zumárraga, M.1
Bulter, T.2
Shleev, S.3
Polaina, J.4
Martínez-Arias, A.5
Plou, F.J.6
Ballesteros, A.7
Alcalde, M.8
-
37
-
-
71549144429
-
-
T. Jerphagnon A. J. A. Gayet F. Berthiol V. Ritleng N. MrŠić A. Meetsma M. Pfeffer A. J. Minnaard B. L. Feringa J. G. de Vries Chem.-Eur. J. 2009 15 12780 12790
-
(2009)
Chem.-Eur. J.
, vol.15
, pp. 12780-12790
-
-
Jerphagnon, T.1
Gayet, A.J.A.2
Berthiol, F.3
Ritleng, V.4
Mršić, N.5
Meetsma, A.6
Pfeffer, M.7
Minnaard, A.J.8
Feringa, B.L.9
De Vries, J.G.10
-
38
-
-
53849084492
-
-
R. M. Haak F. Berthiol T. Jerphagnon A. J. A. Gayet C. Tarabiono C. P. Postema V. Ritleng M. Pfeffer D. B. Janssen A. J. Minnaard B. L. Feringa J. G. de Vries J. Am. Chem. Soc. 2008 130 13508 13509
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13508-13509
-
-
Haak, R.M.1
Berthiol, F.2
Jerphagnon, T.3
Gayet, A.J.A.4
Tarabiono, C.5
Postema, C.P.6
Ritleng, V.7
Pfeffer, M.8
Janssen, D.B.9
Minnaard, A.J.10
Feringa, B.L.11
De Vries, J.G.12
-
39
-
-
28244486843
-
-
T. M. Poessl B. Kosjek U. Ellmer C. C. Gruber K. Edegger K. Faber P. Hildebrandt U. T. Bornscheuer W. Kroutil Adv. Synth. Catal. 2005 347 1827 1834
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1827-1834
-
-
Poessl, T.M.1
Kosjek, B.2
Ellmer, U.3
Gruber, C.C.4
Edegger, K.5
Faber, K.6
Hildebrandt, P.7
Bornscheuer, U.T.8
Kroutil, W.9
-
49
-
-
84861498239
-
-
S. S. van Berkel S. Brauch L. Gabriel M. Henze S. Stark D. Vasilev L. A. Wessjohann M. Abbas B. Westermann Angew. Chem., Int. Ed. 2012 51 5343 5346
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 5343-5346
-
-
Van Berkel, S.S.1
Brauch, S.2
Gabriel, L.3
Henze, M.4
Stark, S.5
Vasilev, D.6
Wessjohann, L.A.7
Abbas, M.8
Westermann, B.9
-
53
-
-
52649137955
-
-
I. Lavandera A. Kern V. Resch B. Ferreira-Silva A. Glieder W. M. F. Fabian S. de Wildeman W. Kroutil Org. Lett. 2008 10 2155 2158
-
(2008)
Org. Lett.
, vol.10
, pp. 2155-2158
-
-
Lavandera, I.1
Kern, A.2
Resch, V.3
Ferreira-Silva, B.4
Glieder, A.5
Fabian, W.M.F.6
De Wildeman, S.7
Kroutil, W.8
-
60
-
-
37849039002
-
-
Another indication that substrate solubilization played an important role in this oxidative reaction was the fact that when alcohol 1a (a crystal solid) was crushed into very tiny pieces, the conversion in plain NaOAc buffer (50 mM, pH 4.5) increased from less than 10% to 47% after 24 h at 20 °C
-
K. Alfonsi J. Colberg P. J. Dunn T. Fevig S. Jennings T. A. Johnson H. P. Kleine C. Knight M. A. Nagy D. A. Perry M. Stefaniak Green Chem. 2008 10 31 36
-
(2008)
Green Chem.
, vol.10
, pp. 31-36
-
-
Alfonsi, K.1
Colberg, J.2
Dunn, P.J.3
Fevig, T.4
Jennings, S.5
Johnson, T.A.6
Kleine, H.P.7
Knight, C.8
Nagy, M.A.9
Perry, D.A.10
Stefaniak, M.11
-
61
-
-
33845516621
-
-
Further experiments oxidizing mixtures of dichlorinated alcohol 1a with monohalogenated derivative 1i or unsubstituted compound 1j afforded, as expected, mixtures of the corresponding ketones in similar ratios (see ESI for more details)
-
I. W. C. E. Ardens Y. Li R. A. Sheldon Biocatal. Biotransform. 2006 24 443 448
-
(2006)
Biocatal. Biotransform.
, vol.24
, pp. 443-448
-
-
Ardens, I.W.C.E.1
Li, Y.2
Sheldon, R.A.3
-
62
-
-
79751476167
-
-
S. A. Tromp I. MatijoŠytė R. A. Sheldon I. W. C. E. Arends G. Mul M. T. Kreutzer J. A. Moulijn S. de Vries ChemCatChem 2010 2 827 833
-
(2010)
ChemCatChem
, vol.2
, pp. 827-833
-
-
Tromp, S.A.1
Matijošyte, I.2
Sheldon, R.A.3
Arends, I.W.C.E.4
Mul, G.5
Kreutzer, M.T.6
Moulijn, J.A.7
De Vries, S.8
-
71
-
-
36348937198
-
-
A recent example can be found in
-
R. A. Sheldon Green Chem. 2007 9 1273 1283
-
(2007)
Green Chem.
, vol.9
, pp. 1273-1283
-
-
Sheldon, R.A.1
-
75
-
-
33744943048
-
-
K. Edegger C. C. Gruber T. M. Poessl S. R. Wallner I. Lavandera K. Faber F. Niehaus J. Eck R. Oehrlein A. Hafner W. Kroutil Chem. Commun. 2006 2402 2404
-
(2006)
Chem. Commun.
, pp. 2402-2404
-
-
Edegger, K.1
Gruber, C.C.2
Poessl, T.M.3
Wallner, S.R.4
Lavandera, I.5
Faber, K.6
Niehaus, F.7
Eck, J.8
Oehrlein, R.9
Hafner, A.10
Kroutil, W.11
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