InspIRED by Nature: NADPH-Dependent Imine Reductases (IREDs) as Catalysts for the Preparation of Chiral Amines.
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Photometric characterization of the reductive amination scope of the imine reductases from Streptomyces tsukubaensis and Streptomyces ipomoeae.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.A Retrosynthesis Approach for Biocatalysis in Organic Synthesis.Holo Structure and Steady State Kinetics of the Thiazolinyl Imine Reductases for Siderophore Biosynthesis.In vivo plug-and-play: a modular multi-enzyme single-cell catalyst for the asymmetric amination of ketoacids and ketonesEnzymatic and Chemoenzymatic Three-Step Cascades for the Synthesis of Stereochemically Complementary Trisubstituted Tetrahydroisoquinolines.The fourth wave of biocatalysis is approaching.Recent advances in imine reductase-catalyzed reactions.Direct Alkylation of Amines with Primary and Secondary Alcohols through Biocatalytic Hydrogen Borrowing.Biocatalytic Routes to Enantiomerically Enriched Dibenz[c,e]azepines.Asymmetric Ketone Reduction by Imine Reductases.The biochemical characterization of three imine-reducing enzymes from Streptosporangium roseum DSM43021, Streptomyces turgidiscabies and Paenibacillus elgii.Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis.NAD(P)H‐Dependent Dehydrogenases for the Asymmetric Reductive Amination of Ketones: Structure, Mechanism, Evolution and Application.Identification of Novel Bacterial Members of the Imine Reductase Enzyme Family that Perform Reductive AminationKinetic Resolution and Deracemization of Racemic Amines Using a Reductive AminaseBiocatalytic Routes to Enantiomerically Enriched Dibenz[c ,e ]azepinesDirect Alkylation of Amines with Primary and Secondary Alcohols through Biocatalytic Hydrogen BorrowingOne-step process for production of N-methylated amino acids from sugars and methylamine using recombinant Corynebacterium glutamicum as biocatalystA general and atom-efficient continuous-flow approach to prepare amines, amides and imines via reactive -chloramines
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P2860
InspIRED by Nature: NADPH-Dependent Imine Reductases (IREDs) as Catalysts for the Preparation of Chiral Amines.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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name
InspIRED by Nature: NADPH-Depe ...... Preparation of Chiral Amines.
@en
InspIRED by Nature: NADPH-Dependent Imine Reductases
@nl
type
label
InspIRED by Nature: NADPH-Depe ...... Preparation of Chiral Amines.
@en
InspIRED by Nature: NADPH-Dependent Imine Reductases
@nl
prefLabel
InspIRED by Nature: NADPH-Depe ...... Preparation of Chiral Amines.
@en
InspIRED by Nature: NADPH-Dependent Imine Reductases
@nl
P2860
P356
P1476
InspIRED by Nature: NADPH-Depe ...... Preparation of Chiral Amines.
@en
P2093
Gideon Grogan
Nicholas J Turner
P2860
P356
10.1002/CHEM.201503954
P407
P577
2015-12-15T00:00:00Z