| 1 |
Highly Efficient Deracemization of Racemic 2-Hydroxy Acids in a Three-Enzyme Co-Expression System Using a Novel Ketoacid Reductase
Xue YP, Wang C, Wang DC, Liu ZQ, Zheng YG
Applied Biochemistry and Biotechnology, 186(3), 563, 2018 |
| 2 |
One-Pot Preparation of d-Amino Acids Through Biocatalytic Deracemization Using Alanine Dehydrogenase and -Transaminase
Han SW, Shin JS
Catalysis Letters, 148(12), 3678, 2018 |
| 3 |
Model of Temperature Cycle-Induced Deracemization via Differences in Crystal Growth Rate Dispersion
Uchin R, Suwannasang K, Flood AE
Chemical Engineering & Technology, 40(7), 1252, 2017 |
| 4 |
Substrate profiling of cyclohexylamine oxidase and its mutants reveals new biocatalytic potential in deracemization of racemic amines
Li GY, Ren J, Iwaki H, Zhang DL, Hasegawa Y, Wu QQ, Feng JH, Lau PCK, Zhu DM
Applied Microbiology and Biotechnology, 98(4), 1681, 2014 |
| 5 |
Complete solid state deracemization by High Pressure Homogenization
Iggland M, Fernandez-Ronco MP, Senn R, Kluge J, Mazzotti M
Chemical Engineering Science, 111, 106, 2014 |
| 6 |
A thermostable L-aspartate oxidase: a new tool for biotechnological applications
Bifulco D, Pollegioni L, Tessaro D, Servi S, Molla G
Applied Microbiology and Biotechnology, 97(16), 7285, 2013 |
| 7 |
Sequential deracemization of sulfoxides via whole-cell resolution and heterogeneous oxidation
Tudorache M, Nica S, Bartha E, Lupan I, Parvulescu VI
Applied Catalysis A: General, 441, 42, 2012 |
| 8 |
Control of helical chirality of poly(quinoxaline-2,3-diyl)s based on postpolymerization modification of the terminal group by small chiral molecules
Nagata Y, Ohashi S, Suginome M
Journal of Polymer Science Part A: Polymer Chemistry, 50(8), 1564, 2012 |
| 9 |
Enhanced performance of lipase-catalyzed kinetic resolution of secondary alcohols in monoether-functionalized ionic liquids
Zhou HC, Chen J, Ye LM, Lin HQ, Yuan YZ
Bioresource Technology, 102(10), 5562, 2011 |
| 10 |
Enhancement of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol to its (S)-enantiomer by a highly productive "two-in-one" resin-based in situ product removal strategy
Hu QS, Xu Y, Nie Y
Bioresource Technology, 101(21), 8461, 2010 |
