-
4
-
-
77951499606
-
-
P.P. Giovannini, P. Pedrini, V. Venturi, G. Fantin, and A. Medici J. Mol. Catal. B: Enzym. 64 2010 113 117
-
(2010)
J. Mol. Catal. B: Enzym.
, vol.64
, pp. 113-117
-
-
Giovannini, P.P.1
Pedrini, P.2
Venturi, V.3
Fantin, G.4
Medici, A.5
-
5
-
-
77952956848
-
-
In a parallel investigation, Müller and co-workers demonstrated that α-hydroxy methyl ketones can be obtained by using a different ThDP-dependent enzyme catalyst and pyruvate as acetyl anion equivalent.
-
In a parallel investigation, Müller and co-workers demonstrated that α-hydroxy methyl ketones can be obtained by using a different ThDP-dependent enzyme catalyst and pyruvate as acetyl anion equivalent. P. Lehwald, M. Richter, C. Röhr, H.-W. Liu, and M. Müller Angew. Chem., Int. Ed. 49 2010 2389 2392
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 2389-2392
-
-
Lehwald, P.1
Richter, M.2
Röhr, C.3
Liu, H.-W.4
Müller, M.5
-
7
-
-
0001417463
-
-
Pioneering observations by Mizuhara and Handler established that the thiamine-promoted reaction of biacetyl and acetaldehyde involved scission of the biacetyl into two moieties to form acetoin and acetate.
-
Pioneering observations by Mizuhara and Handler established that the thiamine-promoted reaction of biacetyl and acetaldehyde involved scission of the biacetyl into two moieties to form acetoin and acetate. S. Mizuhara, and P. Handler J. Am. Chem. Soc. 76 1954 571 573
-
(1954)
J. Am. Chem. Soc.
, vol.76
, pp. 571-573
-
-
Mizuhara, S.1
Handler, P.2
-
12
-
-
33745716505
-
-
For representative examples, see: D. Enders, O. Niemeier, and T. Balensiefer Angew. Chem., Int. Ed. 45 2006 1463 1467
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 1463-1467
-
-
Enders, D.1
Niemeier, O.2
Balensiefer, T.3
-
13
-
-
33745722719
-
-
H. Takikawa, Y. Hachisu, J.W. Bode, and K. Suzuki Angew. Chem., Int. Ed. 45 2006 3492 3494
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 3492-3494
-
-
Takikawa, H.1
Hachisu, Y.2
Bode, J.W.3
Suzuki, K.4
-
17
-
-
78650909553
-
-
For a recent study on highly chemoselective crossed condensations between aliphatic and ortho-substituted aromatic aldehydes, see
-
For a recent study on highly chemoselective crossed condensations between aliphatic and ortho-substituted aromatic aldehydes, see: S.E. O'Toole, C.A. Rose, S. Gundala, K. Zeitler, and S.J. Connon J. Org. Chem. 76 2011 347 357
-
(2011)
J. Org. Chem.
, vol.76
, pp. 347-357
-
-
O'Toole, S.E.1
Rose, C.A.2
Gundala, S.3
Zeitler, K.4
Connon, S.J.5
-
19
-
-
64149099325
-
-
For a recent review, see
-
For a recent review, see: N.S. Nemeria, S. Chakraborty, A. Balakrishnan, and F. Jordan FEBS J. 276 2009 2432 2446
-
(2009)
FEBS J.
, vol.276
, pp. 2432-2446
-
-
Nemeria, N.S.1
Chakraborty, S.2
Balakrishnan, A.3
Jordan, F.4
-
23
-
-
34547926884
-
-
For a detailed study on the 1,2-proton shift involved in this type of intermediate species, see
-
For a detailed study on the 1,2-proton shift involved in this type of intermediate species, see: S. Gronert Org. Lett. 9 2007 3065 3068
-
(2007)
Org. Lett.
, vol.9
, pp. 3065-3068
-
-
Gronert, S.1
-
24
-
-
29944437044
-
-
For a previous study on the preferential reduction of the benzoyl group of 1f, see:, and references therein
-
For a previous study on the preferential reduction of the benzoyl group of 1f, see: E. Toukoniitty, S. Franceschini, A. Vaccari, and D.-Y. Murzin Appl. Catal., A 300 2006 147 154 and references therein
-
(2006)
Appl. Catal., A
, vol.300
, pp. 147-154
-
-
Toukoniitty, E.1
Franceschini, S.2
Vaccari, A.3
Murzin, D.-Y.4
-
30
-
-
80052916195
-
-
PCT Int. Appl. 2006, WO 2006092749 A1 20060908
-
Naef, R.; Jaquier, A. PCT Int. Appl. 2006, WO 2006092749 A1 20060908.
-
-
-
Naef, R.1
Jaquier, A.2
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