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Items: 1 to 20 of 112

1.

Demonstration of redox potential of Metschnikowia koreensis for stereoinversion of secondary alcohols/1,2-diols.

Meena VS, Banoth L, Banerjee UC.

Biomed Res Int. 2014;2014:410530. doi: 10.1155/2014/410530. Epub 2014 Jan 27.

2.
3.

Stereoinversions using microbial redox-reactions.

Carnell AJ.

Adv Biochem Eng Biotechnol. 1999;63:57-72. Review.

PMID:
9933981
4.

Orchestration of concurrent oxidation and reduction cycles for stereoinversion and deracemisation of sec-alcohols.

Voss CV, Gruber CC, Faber K, Knaus T, Macheroux P, Kroutil W.

J Am Chem Soc. 2008 Oct 22;130(42):13969-72. doi: 10.1021/ja804816a. Epub 2008 Sep 27.

PMID:
18821754
5.

Ruthenium-catalyzed sequential reactions: deracemization of secondary benzylic alcohols.

Shimada Y, Miyake Y, Matsuzawa H, Nishibayashi Y.

Chem Asian J. 2007 Mar 5;2(3):393-6.

PMID:
17441175
6.

Chemoselective Pd-catalyzed oxidation of polyols: synthetic scope and mechanistic studies.

Chung K, Banik SM, De Crisci AG, Pearson DM, Blake TR, Olsson JV, Ingram AJ, Zare RN, Waymouth RM.

J Am Chem Soc. 2013 May 22;135(20):7593-602. doi: 10.1021/ja4008694. Epub 2013 May 9.

PMID:
23659308
7.

Brønsted acid catalyzed asymmetric reduction of ketones and acyl silanes using chiral anti-pentane-2,4-diol.

Matsuo J, Hattori Y, Ishibashi H.

Org Lett. 2010 May 21;12(10):2294-7. doi: 10.1021/ol1006532.

PMID:
20408594
8.

A two-step, one-pot enzymatic synthesis of 2-substituted 1,3-diols.

Kalaitzakis D, Smonou I.

J Org Chem. 2010 Dec 17;75(24):8658-61. doi: 10.1021/jo101519t. Epub 2010 Nov 18.

PMID:
21090643
10.
12.

Biocatalytic strategies for the asymmetric synthesis of alpha-hydroxy ketones.

Hoyos P, Sinisterra JV, Molinari F, Alcántara AR, Domínguez de María P.

Acc Chem Res. 2010 Feb 16;43(2):288-99. doi: 10.1021/ar900196n.

PMID:
19908854
13.
14.

Characterization of a putative stereoselective oxidoreductase from Gluconobacter oxydans and its application in producing ethyl (R)-4-chloro-3-hydroxybutanoate ester.

Liu X, Chen R, Yang Z, Wang J, Lin J, Wei D.

Mol Biotechnol. 2014 Apr;56(4):285-95. doi: 10.1007/s12033-013-9707-z.

PMID:
24113812
15.

Deracemization of secondary alcohols by chemo-enzymatic sequence with plant cells.

Magallanes-Noguera C, Ferrari MM, Kurina-Sanz M, Orden AA.

J Biotechnol. 2012 Aug 31;160(3-4):189-94. doi: 10.1016/j.jbiotec.2012.03.015. Epub 2012 Mar 28.

PMID:
22475681
16.

Asymmetric reduction and oxidation of aromatic ketones and alcohols using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus.

Musa MM, Ziegelmann-Fjeld KI, Vieille C, Zeikus JG, Phillips RS.

J Org Chem. 2007 Jan 5;72(1):30-4.

PMID:
17194078
17.
18.

Highly stereoselective reduction of prochiral ketones by a bacterial reductase coupled with cofactor regeneration.

Ni Y, Li CX, Wang LJ, Zhang J, Xu JH.

Org Biomol Chem. 2011 Aug 7;9(15):5463-8. doi: 10.1039/c1ob05285c. Epub 2011 Jun 14.

PMID:
21670841
19.

Tandem concurrent processes: one-pot single-catalyst biohydrogen transfer for the simultaneous preparation of enantiopure secondary alcohols.

Bisogno FR, Lavandera I, Kroutil W, Gotor V.

J Org Chem. 2009 Feb 20;74(4):1730-2. doi: 10.1021/jo802350f.

PMID:
19138072
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