Highly enantioselective reduction of beta,beta-disubstituted aromatic nitroalkenes catalyzed by Clostridium sporogenes.
about
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 HomologuesBiocatalytic Asymmetric Alkene Reduction: Crystal Structure and Characterization of a Double Bond Reductase from Nicotiana tabacumSynthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox CatalysisA General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst.Structure-Based Insight into the Asymmetric Bioreduction of the C=C Double Bond of alpha,beta-Unsaturated Nitroalkenes by Pentaerythritol Tetranitrate Reductase.Asymmetric Reduction of Activated Alkenes by Pentaerythritol Tetranitrate Reductase: Specificity and Control of Stereochemical Outcome by Reaction Optimisation.A short, chemoenzymatic route to chiral beta-aryl-gamma-amino acids using reductases from anaerobic bacteria.Highly enantioselective reduction of α-methylated nitroalkenes.Rh-catalyzed highly enantioselective hydrogenation of nitroalkenes under basic conditions.Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase.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.Enantioselective iridium-catalyzed hydrogenation of β,β-disubstituted nitroalkenes.Asymmetric transfer hydrogenation of 3-nitroquinolines: facile access to cyclic nitro compounds with two contiguous stereocenters.A 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 nitroolefinsEne Reductase-Catalysed Synthesis of (R)-Profen DerivativesChemoenzymatic One-Pot Synthesis of γ-Butyrolactones
P2860
Q27666872-C75F19FE-8093-4A59-BA95-DB984AEB3664Q27677485-C4F97228-1456-49F5-83DC-83352A8FBC86Q28829782-DF5C759C-602A-4D53-97E5-521095E0962CQ36420582-5905CEB5-D8EF-431B-A670-2407245CC327Q39533886-3E1B0160-639A-40F1-B541-897F5389C784Q40024861-3FED6CD7-E4B7-4E93-A101-E8B6DAA2CD60Q40025162-89D2DE06-F4DA-4075-9AE8-F630ABF2B8FCQ43187803-32180AC8-CE8F-4317-AC91-3E74D165E7A3Q44889132-2D64CE7D-19A6-461E-A7DC-63CD47BC2914Q45760624-C5D5F07B-C006-4391-8EAF-8ED6CC3415A9Q46216144-75B117E5-E081-4FCE-8853-95C413D9709EQ47373176-F5318F6A-56C0-44D2-B1B3-3D4D457C0E93Q51019045-DD3DF74F-3B2B-4821-A6F0-6CF4F7DA3D38Q53202859-F5CB96D1-2BBB-455A-81C7-78359A0B44F3Q53748827-2CD47760-EE86-4F38-AD2B-F15DCE3926C0Q57979274-D4028EC1-926C-481D-8BA6-EE32F911C65DQ57979276-C5F0047F-8095-4B38-9580-A1AE2FFFADADQ58072000-316B0216-9D29-4DD2-B768-B5F84342785FQ58072059-4E54D2D8-3B61-45BA-8F8C-A1E43E7B532F
P2860
Highly enantioselective reduction of beta,beta-disubstituted aromatic nitroalkenes catalyzed by Clostridium sporogenes.
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@ast
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@en
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@nl
type
label
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@ast
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@en
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@nl
prefLabel
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@ast
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@en
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@nl
P356
P1476
Highly enantioselective reduct ...... zed by Clostridium sporogenes.
@en
P2093
John M Gardiner
Karl Fisher
P304
P356
10.1021/JO800124V
P407
P577
2008-05-02T00:00:00Z