| P2093 | author name string | Xi Chen | |
| | Ting Mei | |
| | Yunfeng Cui | |
| | Dunming Zhu | |
| | Xiangtao Liu | |
| | Jinhui Feng | |
| | Qiaqing Wu | |
| | Qijia Chen | |
| P2860 | cites work | Characterization of short-chain dehydrogenase/reductase homologues of Escherichia coli (YdfG) and Saccharomyces cerevisiae (YMR226C). | Q27934218 |
| | Efficient anaerobic whole cell stereoselective bioreduction with recombinant saccharomyces cerevisiae | Q27936216 |
| | Carbonyl reductase SCRII from Candida parapsilosis catalyzes anti-Prelog reaction to (S)-1-phenyl-1,2-ethanediol with absolute stereochemical selectivity | Q33690342 |
| | Novel anti-Prelog stereospecific carbonyl reductases from Candida parapsilosis for asymmetric reduction of prochiral ketones | Q33926173 |
| | Stereospecific dihydroxylation of the styrene vinyl group by purified naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4 | Q35608226 |
| | Purification, characterization, gene cloning, and expression of a novel alcohol dehydrogenase with anti-prelog stereospecificity from Candida parapsilosis | Q35913044 |
| | Critical residues for structure and catalysis in short-chain dehydrogenases/reductases | Q38289818 |
| | Chiral ruthenabicyclic complexes: precatalysts for rapid, enantioselective, and wide-scope hydrogenation of ketones | Q44074037 |
| | Aerial oxidation of the glucocorticoid side-chain under pH control | Q46719867 |
| | Highly enantioselective oxidation of racemic phenyl-1,2-ethanediol to optically pure (R)-(-)-mandelic acid by a newly isolated Brevibacterium lutescens CCZU12-1. | Q48038965 |
| | Highly enantioselective and efficient synthesis of methyl (R)-o-chloromandelate with recombinant E. coli: toward practical and green access to clopidogrel. | Q50690752 |
| | Asymmetric hydrogenation of alpha-hydroxy ketones catalyzed by MsDPEN-Cp*Ir(III) complex. | Q50998634 |
| | Highly efficient synthesis of (R)-3-quinuclidinol in a space-time yield of 916 g L(-1) d(-1) using a new bacterial reductase ArQR. | Q54303665 |
| | Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. | Q54459180 |
| | Efficient Reduction of Ethyl 2-Oxo-4-phenylbutyrate at 620ā
gā
Lā1 by a Bacterial Reductase with Broad Substrate Spectrum | Q57189280 |
| | Enzymatic resolution of 1-phenyl-1,2-ethanediol by enantioselective oxidation: Overcoming product inhibition by continuous extraction | Q61660676 |
| | Efficient Enantioselective Synthesis of Optically Active Diols by Asymmetric Hydrogenation with Modular Chiral Metal Catalysts | Q64024415 |
| | Microbial transformation of 2-hydroxy and 2-acetoxy ketones with Geotrichum sp | Q73958354 |
| | Molecular cloning and overexpression of the gene encoding an NADPH-dependent carbonyl reductase from Candida magnoliae, involved in stereoselective reduction of ethyl 4-chloro-3-oxobutanoate | Q74179731 |
| | Crystallization-induced diastereoselection: asymmetric synthesis of substance P inhibitors | Q77841018 |
| | Asymmetric reduction of ketones with recombinant E. coli whole cells in neat substrates | Q82062459 |
| | Stereoselective enzymatic synthesis of chiral alcohols with the use of a carbonyl reductase from Candida magnoliae with anti-Prelog enantioselectivity | Q83366505 |
| P433 | issue | 4 | |
| P304 | page(s) | 483-488 | |
| P577 | publication date | 2015-04-30 | |
| P1433 | published in | ChemistryOpen | Q19277289 |
| P1476 | title | Highly Efficient Synthesis of Optically Pure (S)-1-phenyl-1,2-ethanediol by a Self-Sufficient Whole Cell Biocatalyst | |
| P478 | volume | 4 | |