Prelog and anti-Prelog stereoselectivity of two ketoreductases from Candida glabrata

[1]  Jian‐He Xu,et al.  Stereospecific Reduction of Methyl o‐Chlorobenzoylformate at 300 g⋅L−1 without Additional Cofactor using a Carbonyl Reductase Mined from Candida glabrata , 2012 .

[2]  G. Huisman,et al.  Engineering the third wave of biocatalysis , 2012, Nature.

[3]  Jian‐He Xu,et al.  Efficient synthesis of a chiral precursor for angiotensin-converting enzyme (ACE) inhibitors in high space-time yield by a new reductase without external cofactors. , 2012, Organic letters.

[4]  I. Arends,et al.  Enzymatic reductions for the chemist , 2011 .

[5]  A. Bommarius,et al.  Enantioenriched compounds via enzyme-catalyzed redox reactions. , 2011, Chemical reviews.

[6]  Jack Liang,et al.  Practical chiral alcohol manufacture using ketoreductases. , 2010, Current opinion in chemical biology.

[7]  Vesna Mitchell,et al.  Development of a Biocatalytic Process as an Alternative to the (−)-DIP-Cl-Mediated Asymmetric Reduction of a Key Intermediate of Montelukast , 2010 .

[8]  Jack Liang,et al.  Highly Enantioselective Reduction of a Small Heterocyclic Ketone: Biocatalytic Reduction of Tetrahydrothiophene-3-one to the Corresponding (R)-Alcohol , 2010 .

[9]  Dunming Zhu,et al.  Asymmetric Synthesis of Both Antipodes of β-Hydroxy Nitriles and β-Hydroxy Carboxylic Acids via Enzymatic Reduction or Sequential Reduction/Hydrolysis. , 2009 .

[10]  Haribabu Ankati,et al.  Asymmetric synthesis of both antipodes of beta-hydroxy nitriles and beta-hydroxy carboxylic acids via enzymatic reduction or sequential reduction/hydrolysis. , 2009, The Journal of organic chemistry.

[11]  A. Henriksen,et al.  Barley aldose reductase: Structure, cofactor binding, and substrate recognition in the aldo/keto reductase 4C family , 2008, Proteins.

[12]  Oliver May,et al.  Biocatalytic reductions: from lab curiosity to "first choice". , 2007, Accounts of chemical research.

[13]  S. Kamitori,et al.  X-ray structures of NADPH-dependent carbonyl reductase from Sporobolomyces salmonicolor provide insights into stereoselective reductions of carbonyl compounds. , 2005, Journal of molecular biology.

[14]  H. Sahm,et al.  Enantioselective reduction of carbonyl compounds by whole-cell biotransformation, combining a formate dehydrogenase and a (R)-specific alcohol dehydrogenase , 2005, Applied Microbiology and Biotechnology.

[15]  V. Prelog.  Specification of the stereospecificity of some oxido-reductases by diamond lattice sections , 1964 .

[16]  John H. Grate,et al.  A green-by-design biocatalytic process for atorvastatin intermediate , 2010 .