A One-Step Biocatalytic Process for (S)-4-Chloro-3-hydroxybutyronitrile using Halohydrin Dehalogenase: A Chiral Building Block for Atorvastatin
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A One-Step Biocatalytic Process for (S)-4-Chloro-3-hydroxybutyronitrile using Halohydrin Dehalogenase: A Chiral Building Block for Atorvastatin
Authors
Keywords
-
Journal
ChemCatChem
Volume 7, Issue 16, Pages 2446-2450
Publisher
Wiley
Online
2015-07-25
DOI
10.1002/cctc.201500453
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A highly efficient designer cell for enantioselective reduction of ketones
- (2015) Gautam Srivastava et al. Catalysis Science & Technology
- A broadly applicable and practical oligomeric (salen)Co catalyst for enantioselective epoxide ring-opening reactions
- (2014) David E. White et al. TETRAHEDRON
- Synthesis of ethyl (R)-4-cyano-3-hydroxybutyrate in high concentration using a novel halohydrin dehalogenase HHDH-PL from Parvibaculum lavamentivorans DS-1
- (2014) Nan-Wei Wan et al. RSC Advances
- Chemical and enzymatic approaches to the synthesis of optically pure ethyl (R)-4-cyano-3-hydroxybutanoate
- (2013) Zhong-Yu You et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Biocatalytic and Structural Properties of a Highly Engineered Halohydrin Dehalogenase
- (2013) Marcus Schallmey et al. CHEMBIOCHEM
- Substrate promiscuity of cytochrome P450 RhF
- (2013) Elaine O'Reilly et al. Catalysis Science & Technology
- Novel highly active polymer supported chiral Co(III)–salen catalysts for hydrolytic kinetic resolution of epichlorohydrin
- (2012) Katarzyna Matkiewicz et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
- Immobilized Aspergillus niger epoxide hydrolases: Cost-effective biocatalysts for the prepation of enantiopure styrene oxide, propylene oxide and epichlorohydrin
- (2012) Deniz Yildirim et al. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
- Catalytic activity of halohydrin dehalogenases towards spiroepoxides
- (2012) Maja Majerić Elenkov et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Highly efficient synthesis of chiral alcohols with a novel NADH-dependent reductase from Streptomyces coelicolor
- (2011) Li-Juan Wang et al. BIORESOURCE TECHNOLOGY
- Recent advances in alcohol dehydrogenase-catalyzed asymmetric production of hydrophobic alcohols
- (2011) Musa M. Musa et al. Catalysis Science & Technology
- Biocatalytic Redox Reactions for Organic Synthesis: Nonconventional Regeneration Methods
- (2010) Frank Hollmann et al. ChemCatChem
- One pot ‘click’ reactions: tandem enantioselective biocatalytic epoxide ring opening and [3+2] azide alkyne cycloaddition
- (2010) Lachlan S. Campbell-Verduyn et al. CHEMICAL COMMUNICATIONS
- A high-throughput colorimetric assay for screening halohydrin dehalogenase saturation mutagenesis libraries
- (2010) Lixia Tang et al. JOURNAL OF BIOTECHNOLOGY
- Resolution of 2,2-Disubstituted Epoxides via Biocatalytic Azidolysis
- (2010) Carmela Molinaro et al. ORGANIC LETTERS
- A green-by-design biocatalytic process for atorvastatin intermediate
- (2009) Steven K. Ma et al. GREEN CHEMISTRY
- Direct preparation of dichloropropanol (DCP) from glycerol using heteropolyacid (HPA) catalysts: A catalyst screen study
- (2008) Sang Hee Lee et al. CATALYSIS COMMUNICATIONS
- Catalytic Promiscuity of Halohydrin Dehalogenase and its Application in Enantioselective Epoxide Ring Opening
- (2008) Ghannia Hasnaoui-Dijoux et al. CHEMBIOCHEM
- Production of Biodiesel through Base-Catalyzed Transesterification of Safflower Oil Using an Optimized Protocol
- (2008) Umer Rashid et al. ENERGY & FUELS
- Formation of Enantiopure 5-Substituted Oxazolidinones through Enzyme-Catalysed Kinetic Resolution of Epoxides
- (2008) Maja Majerić Elenkov et al. ORGANIC LETTERS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started