Enantioselective Ring Opening of Epoxides with Cyanide Catalysed by Halohydrin Dehalogenases: A New Approach to Non‐Racemic β‐Hydroxy Nitriles
- 2 March 2006
- journal article
- research article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 348 (4-5) , 579-585
- https://doi.org/10.1002/adsc.200505333
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Enantioselective C–C bond synthesis catalysed by enzymesChemical Society Reviews, 2005
- An Enzyme Library Approach to Biocatalysis: Development of Nitrilases for Enantioselective Production of Carboxylic Acid DerivativesJournal of the American Chemical Society, 2002
- Exploration of the biocatalytic potential of a halohydrin dehalogenase using chromogenic substratesTetrahedron: Asymmetry, 2002
- Halohydrin Dehalogenases Are Structurally and Mechanistically Related to Short-Chain Dehydrogenases/ReductasesJournal of Bacteriology, 2001
- Enantio- and chemoselective bioreduction of β-keto nitriles by the fungus Curvularia lunataTetrahedron: Asymmetry, 2000
- Microbiological transformations 41.Journal of Molecular Catalysis B: Enzymatic, 1998
- Thiacrown Ether Technology in Lipase-Catalyzed Reaction: Scope and Limitation for Preparing Optically Active 3-Hydroxyalkanenitriles and Application to Insect Pheromone SynthesisThe Journal of Organic Chemistry, 1997
- The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvementThe Journal of Organic Chemistry, 1992
- A new catalytic function of halohydrin hydrogen-halide-lyase, synthesis of β-hydroxynitriles from epoxides and cyanideBiochemical and Biophysical Research Communications, 1991
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982