Asymmetric Reduction of Activated Alkenes by Pentaerythritol Tetranitrate Reductase: Specificity and Control of Stereochemical Outcome by Reaction Optimisation.
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A site-saturated mutagenesis study of pentaerythritol tetranitrate reductase reveals that residues 181 and 184 influence ligand binding, stereochemistry and reactivityThe Structure of Glycerol Trinitrate Reductase NerA fromAgrobacterium radiobacterReveals the Molecular Reason for Nitro- and Ene-Reductase Activity in OYE HomologuesCrystal structure determination and mutagenesis analysis of the ene reductase NCRBiocatalytic Asymmetric Alkene Reduction: Crystal Structure and Characterization of a Double Bond Reductase from Nicotiana tabacumSTRUCTURAL AND FUNCTIONAL CONSEQUENCES OF CIRCULAR PERMUTATION ON THE ACTIVE SITE OF OLD YELLOW ENZYMEIsolation and characterization of a thermotolerant ene reductase from Geobacillus sp. 30 and its heterologous expression in Rhodococcus opacus.Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.Carbon-carbon double-bond reductases in nature.Structural insights into the ene-reductase synthesis of profens.Light-driven biocatalytic reduction of α,β-unsaturated compounds by ene reductases employing transition metal complexes as photosensitizers.Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductasesNAD(P)H-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor.Nitrile as Activating Group in the Asymmetric Bioreduction of β-Cyanoacrylic Acids Catalyzed by Ene-ReductasesFunctional characterization and stability improvement of a 'thermophilic-like' ene-reductase from Rhodococcus opacus 1CPNanofibrillar Peptide hydrogels for the immobilization of biocatalysts for chemical transformations.Excited state dynamics can be used to probe donor-acceptor distances for H-tunneling reactions catalyzed by flavoproteins.Better than Nature: Nicotinamide Biomimetics That Outperform Natural CoenzymesA short, chemoenzymatic route to chiral beta-aryl-gamma-amino acids using reductases from anaerobic bacteria.Rh-catalyzed highly enantioselective hydrogenation of nitroalkenes under basic conditions.Formation of δ-Lactones with anti-Baeyer-Villiger Regiochemistry: Investigations into the Mechanism of the Cerium-Catalyzed Aerobic Coupling of β-Oxoesters with Enol Acetates.Production of flavours and fragrances via bioreduction of (4R)-(-)-carvone and (1R)-(-)-myrtenal by non-conventional yeast whole-cells.Recombinant expression and characterisation of the oxygen-sensitive 2-enoate reductase from Clostridium sporogenes.An enoate reductase Achr-OYE4 from Achromobacter sp. JA81: characterization and application in asymmetric bioreduction of C=C bonds.Systematic methodology for the development of biocatalytic hydrogen-borrowing cascades: application to the synthesis of chiral α-substituted carboxylic acids from α-substituted α,β-unsaturated aldehydes.Comparative characterization of novel ene-reductases from cyanobacteria.Rhodococcus strains as source for ene-reductase activity.Enzyme engineering toolbox – a ‘catalyst’ for changeA surprising observation that oxygen can affect the product enantiopurity of an enzyme-catalysed reactionActive site modifications in pentaerythritol tetranitrate reductase can lead to improved product enantiopurity, decreased by-product formation and altered stereochemical outcome in reactions with α,β-unsaturated nitroolefinsCatalytic Performance of a Class III Old Yellow Enzyme and Its Cysteine Variants
P2860
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P2860
Asymmetric Reduction of Activated Alkenes by Pentaerythritol Tetranitrate Reductase: Specificity and Control of Stereochemical Outcome by Reaction Optimisation.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Asymmetric Reduction of Activa ...... come by Reaction Optimisation.
@en
type
label
Asymmetric Reduction of Activa ...... come by Reaction Optimisation.
@en
prefLabel
Asymmetric Reduction of Activa ...... come by Reaction Optimisation.
@en
P2093
P2860
P50
P1476
Asymmetric Reduction of Activa ...... tcome by Reaction Optimisation
@en
P2093
John M Gardiner
Michiyo Sakuma
Nigel S Scrutton
P2860
P304
P356
10.1002/ADSC.200900574
10.1002/ADSC.200900603
P577
2009-11-01T00:00:00Z