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Selective Ring‐Opening of Di‐Substituted Epoxides Catalysed by Halohydrin Dehalogenases.
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- ChemCatChem, 2019, v. 11, n. 8, p. 2099, doi. 10.1002/cctc.201900103
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- Article
Covalent immobilization of halohydrin dehalogenase for efficient synthesis of epichlorohydrin in an integrated bioreactor.
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- Biotechnology Progress, 2018, v. 34, n. 3, p. 784, doi. 10.1002/btpr.2617
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- Article
Dehalogenases: From Improved Performance to Potential Microbial Dehalogenation Applications.
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- Molecules, 2018, v. 23, n. 5, p. 1100, doi. 10.3390/molecules23051100
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- Article
Identification and Characterization of a Novel Halohydrin Dehalogenase from <italic>Bradyrhizobium erythrophlei</italic> and Its Performance in Preparation of Both Enantiomers of Epichlorohydrin.
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- Catalysis Letters, 2018, v. 148, n. 4, p. 1181, doi. 10.1007/s10562-017-2292-1
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- Article
A concise synthesis of 25-hydroxycholesterol from hyodesoxycholic acid.
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- Journal of Chemical Research, 2018, v. 42, p. 96, doi. 10.3184/174751918X15184426915885
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- Article
A concise synthesis of 25-hydroxycholesterol from hyodesoxycholic acid.
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- Journal of Chemical Research, 2018, v. 42, n. 2, p. 96, doi. 10.3184/174751918X15184426915885
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- Article
Investigation of Halohydrins Degradation by Whole Cells and Cell-free Extract of Pseudomonas putida DSM 437: A Kinetic Approach.
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- Chemical & Biochemical Engineering Quarterly, 2017, v. 31, n. 3, p. 233, doi. 10.15255/CABEQ.2016.924
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- Article
Exploring the thermostable properties of halohydrin dehalogenase from Agrobacterium radiobacter AD1 by a combinatorial directed evolution strategy.
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- Applied Microbiology & Biotechnology, 2017, v. 101, n. 8, p. 3201, doi. 10.1007/s00253-017-8090-2
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- Article
A robust cosolvent-compatible halohydrin dehalogenase by computational library design.
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- PEDS: Protein Engineering, Design & Selection, 2017, v. 30, n. 3, p. 173, doi. 10.1093/protein/gzw068
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- Article
Transformation of Tertiary Benzyl Alcohols into the Vicinal Halo-Substituted Derivatives Using N-Halosuccinimides.
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- Molecules, 2016, v. 21, n. 10, p. 1325, doi. 10.3390/molecules21101325
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- Article
Recent advances on halohydrin dehalogenases-from enzyme identification to novel biocatalytic applications.
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- Applied Microbiology & Biotechnology, 2016, v. 100, n. 18, p. 7827, doi. 10.1007/s00253-016-7750-y
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- Article
Biochemical and biocatalytic characterization of 17 novel halohydrin dehalogenases.
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- Applied Microbiology & Biotechnology, 2016, v. 100, n. 17, p. 7517, doi. 10.1007/s00253-016-7493-9
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- Article
Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 12, p. 2110, doi. 10.1002/ejoc.201600286
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- Article
A One-Step Biocatalytic Process for ( S)-4-Chloro-3-hydroxybutyronitrile using Halohydrin Dehalogenase: A Chiral Building Block for Atorvastatin.
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- ChemCatChem, 2015, v. 7, n. 16, p. 2446, doi. 10.1002/cctc.201500453
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- Article
A high-throughput adrenaline test for the exploration of the catalytic potential of halohydrin dehalogenases in epoxide ring-opening reactions.
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- Biotechnology & Applied Biochemistry, 2015, v. 62, n. 4, p. 451, doi. 10.1002/bab.1278
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- Article
Oxazolidinone Synthesis through Halohydrin Dehalogenase- Catalyzed Dynamic Kinetic Resolution.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 8, p. 1709, doi. 10.1002/adsc.201500111
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- Article
Efficient Biosynthesis of Ethyl (R)-3-Hydroxyglutarate through a One-Pot Bienzymatic Cascade of Halohydrin Dehalogenase and Nitrilase.
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- 2015
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- Interview
An efficient high-throughput screening assay for rapid directed evolution of halohydrin dehalogenase for preparation of β-substituted alcohols.
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- Applied Microbiology & Biotechnology, 2015, v. 99, n. 9, p. 4019, doi. 10.1007/s00253-015-6527-z
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- Article
Chiral Chlorohydrins from the Biocatalyzed Reduction of Chloroketones: Chiral Building Blocks for Antiretroviral Drugs.
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- ChemCatChem, 2015, v. 7, n. 6, p. 984, doi. 10.1002/cctc.201403023
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- Article
Highly Enantioselective Production of (R)-Halohydrins with Whole Cells of Rhodotorula rubra KCh 82 Culture.
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- International Journal of Molecular Sciences, 2014, v. 15, n. 12, p. 22392, doi. 10.3390/ijms151222392
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Purification, Gene Cloning, and Characterization of a Novel Halohydrin Dehalogenase from Agromyces mediolanus ZJB120203.
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- Applied Biochemistry & Biotechnology, 2014, v. 174, n. 1, p. 352, doi. 10.1007/s12010-014-1111-z
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- Article
Expression, characterization, and improvement of a newly cloned halohydrin dehalogenase from Agrobacterium tumefaciens and its application in production of epichlorohydrin.
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- Journal of Industrial Microbiology & Biotechnology, 2014, v. 41, n. 7, p. 1145, doi. 10.1007/s10295-014-1443-2
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- Article
On the Configurational Stability of Chiral, Nonracemic Fluoro- and Iodo-[D<sub>1</sub>]Methyllithiums.
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- Chemistry - A European Journal, 2014, v. 20, n. 14, p. 4086, doi. 10.1002/chem.201304766
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- Article
Identification of halohydrin dehalogenase mutants that resist COBE inhibition.
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- Biotechnology & Bioprocess Engineering, 2014, v. 19, n. 1, p. 26, doi. 10.1007/s12257-013-0457-3
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- Article
Multi-Enzymatic Biosynthesis of Chiral β-Hydroxy Nitriles through Co-Expression of Oxidoreductase and Halohydrin Dehalogenase.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 16, p. 3179, doi. 10.1002/adsc.201300549
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- Article
Novel chiral tool, ( R)-2-octanol dehydrogenase, from Pichia finlandica: purification, gene cloning, and application for optically active α-haloalcohols.
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- Applied Microbiology & Biotechnology, 2013, v. 97, n. 18, p. 8087, doi. 10.1007/s00253-012-4643-6
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- Article
Versatile and efficient method for synthesis of β-halohydrins via regioselective ring opening reaction of epoxides using cross-linked poly (4-vinylpyridine) supported HCl and HBr under solvent-free conditions.
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- Journal of Polymer Research, 2013, v. 20, n. 8, p. 1, doi. 10.1007/s10965-013-0208-3
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- Article