about
Recent Advances in Dynamic Kinetic Resolution by Chiral Bifunctional (Thio)urea- and Squaramide-Based OrganocatalystsContinuous Reusability using Immobilized HasApf in Chemoenzymatic Deracemization: A New Heterogeneous Enzyme CatalysisAcidic lipase Lip I.3 from a Pseudomonas fluorescens-like strain displays unusual properties and shows activity on secondary alcohols.Catalytic Stereoinversion of L-Alanine to Deuterated D-Alanine.Recent biocatalytic oxidation-reduction cascades.Features and technical applications of ω-transaminases.Inverting hydrolases and their use in enantioconvergent biotransformations.Biocatalytic Friedel-Crafts Acylation and Fries Reaction.Deracemization by simultaneous bio-oxidative kinetic resolution and stereoinversion.One-Pot Deracemization of sec-Alcohols: Enantioconvergent Enzymatic Hydrolysis of Alkyl Sulfates Using Stereocomplementary Sulfatases.Demonstration of redox potential of Metschnikowia koreensis for stereoinversion of secondary alcohols/1,2-diols.Stereochemistry and Mechanism of Enzymatic and Non-Enzymatic Hydrolysis of Benzylic sec-Sulfate Esters.Single-operation deracemization of 3H-indolines and tetrahydroquinolines enabled by phase separation.One-pot deracemization of sec-alcohols: enantioconvergent enzymatic hydrolysis of alkyl sulfates using stereocomplementary sulfatases.Asymmetric synthesis of chiral cyclic amine from cyclic imine by bacterial whole-cell catalyst of enantioselective imine reductase.The role of biocatalysis in the asymmetric synthesis of alkaloids.Asymmetric Preparation of prim-, sec-, and tert-Amines Employing Selected Biocatalysts.Coupling biocatalysis and click chemistry: one-pot two-step convergent synthesis of enantioenriched 1,2,3-triazole-derived diols.Expanding dynamic kinetic protocols: transaminase-catalyzed synthesis of α-substituted β-amino ester derivatives.Highly stereoselective recognition and deracemization of amino acids by supramolecular self-assembly.A NADPH-dependent (S)-imine reductase (SIR) from Streptomyces sp. GF3546 for asymmetric synthesis of optically active amines: purification, characterization, gene cloning, and expression.Artificial multi-enzyme networks for the asymmetric amination of sec-alcohols.A computational study of the CO dissociation in cyclopentadienyl ruthenium complexes relevant to the racemization of alcohols.Enzymatic cascades for the stereo-complementary epimerisation of in situ generated epoxy alcohols.Organocatalytic Redox Deracemization of Cyclic Benzylic Ethers Enabled by An Acetal Pool Strategy.Combination of enzyme- and Lewis acid-catalyzed reactions: a new method for the synthesis of 6,7-dihydrobenzofuran-4(5H)-ones starting from 2,5-dimethylfuran and 1,3-cyclohexanediones.Biocatalytic oxidation reactions - a Chemist's perspective.Amination of Ketones by Employing Two New (S)-Selective ω-Transaminases and the His-Tagged ω-TA from Vibrio fluvialisThe Substrate Spectrum of the Inverting sec-Alkylsulfatase Pisa1Kinetic Resolution and Deracemization of Racemic Amines Using a Reductive AminaseDeracemisation of benzylisoquinoline alkaloids employing monoamine oxidase variantsMonoamine Oxidase-ω-Transaminase Cascade for the Deracemisation and Dealkylation of Amines
P2860
Q28067071-47F05D11-137B-479D-9774-7D07FA0F020FQ28818437-87573F29-203D-4B4E-9FDA-EE3F35494247Q30578796-F138A576-2F6F-4028-986B-57D0D1600EDCQ30977173-FDE96803-C63B-4003-8861-13EB626A33C6Q37815710-E75D60D4-B542-478D-B3FC-FAE241F10651Q38007391-E21E4719-F03B-4B63-BBBC-16E29E3B777DQ38117861-0F032FA2-ABE4-4B07-A26D-96B7C01D97BEQ41019843-86CCBFF0-5995-4C47-A933-71DCDB6CDEA8Q41125445-73FCFFF4-0FC3-4B92-9911-04D12FECD6A9Q41142703-5976FBD3-03E0-4047-BCF7-0CE34364DB5DQ41886381-3E4C7EC2-EBA6-4BE7-8A76-DDC04CAAC11AQ41895855-41CF3815-5A5A-4B94-A959-9D6E1E40B780Q42234666-F901F746-BAE6-47E4-9FDF-D091657AA738Q42554148-8A576A4D-3EAF-4E60-ABE2-3E1D67F26FFBQ42915981-6310E89C-705A-422F-99F6-B0C9B7020864Q43092724-BE24EACA-1C64-4F66-BB07-60D8FFF4F7FEQ43120278-C531EF47-E8D1-4032-AB5D-8D0F5BACC4DBQ44244306-FCD9E98D-72F9-4878-BF9E-F93EA33931DCQ45344485-B09599DF-F22D-4034-AD1F-02129D63E163Q45735776-B33749DC-C7C5-4C5B-9EC2-CA7A2D57F0EBQ45972232-52791171-F192-4214-90E1-D67DE34A7570Q46177883-A99EB67E-734C-419C-BB58-928150A71CD7Q46377187-FB95B1C7-1241-4883-B52E-A43D0AFB54F4Q48156261-0E3DD41E-A21C-4E95-AB53-56CCD769111BQ50664212-67B6F99C-1668-4F69-BF1D-9C35670D57E4Q53097210-14849A5A-58C4-440D-92EF-79B49E682C3CQ53835321-6298353E-A548-4588-8222-3468AED30FF0Q57260225-AA287154-AB47-4B2A-B2B6-636105715408Q57978246-D71AA1BE-44AE-4A81-A5A2-7674A3B7CD53Q58048461-4AB1A8D0-C83C-4DD0-89C9-C6B9BB8B3878Q58048616-63F13FF8-C86F-4F3B-B82C-4E982FE3C179Q58048653-DDE411F2-47DE-42D9-9725-1C1203FBDBBA
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 13 January 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Deracemisation methods.
@en
Deracemisation methods.
@nl
type
label
Deracemisation methods.
@en
Deracemisation methods.
@nl
prefLabel
Deracemisation methods.
@en
Deracemisation methods.
@nl
P1476
Deracemisation methods.
@en
P304
P356
10.1016/J.CBPA.2009.11.027
P577
2010-01-13T00:00:00Z