Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: the first asymmetric cross-benzoin condensation.
about
Building Bridges: Biocatalytic C–C-Bond Formation toward Multifunctional ProductsSnapshot of a Reaction Intermediate: Analysis of Benzoylformate Decarboxylase in Complex with a Benzoylphosphonate Inhibitor †Organocatalytic Reactions Enabled by N-Heterocyclic CarbenesLanthanum tricyanide-catalyzed acyl silane-ketone benzoin additions and kinetic resolution of resultant alpha-silyloxyketones.The Catalytic Asymmetric Intramolecular Stetter Reaction.Dynamic kinetic asymmetric cross-benzoin additions of β-stereogenic α-keto esters.A standard numbering scheme for thiamine diphosphate-dependent decarboxylases.The RuO4-catalysed dihydroxylation, ketohydroxylation and mono oxidation--novel oxidation reactions for the synthesis of diols and alpha-hydroxy ketones.Stereocontrolled synthesis of α-amino-α'-alkoxy ketones by a copper-catalyzed cross-coupling of peptidic thiol esters and α-alkoxyalkylstannanes.Carbene catalystsLanthanum tricyanide-catalyzed acyl silane-ketone benzoin additions.A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis.Using site-saturation mutagenesis to explore mechanism and substrate specificity in thiamin diphosphate-dependent enzymes.Functional diversity of organic molecule enzyme cofactors.Engineering stereoselectivity of ThDP-dependent enzymes.Influence of Organic Solvents on Enzymatic Asymmetric CarboligationsRate and equilibrium constants for the addition of N-heterocyclic carbenes into benzaldehydes: a remarkable 2-substituent effect.Catalytic asymmetric cross-aza-benzoin reactions of aliphatic aldehydes with N-Boc-protected imines.Rate and Equilibrium Constants for the Addition of N-Heterocyclic Carbenes into Benzaldehydes: A Remarkable 2-Substituent Effect.N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis.N-heterocyclic-carbene-catalyzed one-pot synthesis of hydroxamic esters.Galactose oxidase model: biomimetic enantiomer-differentiating oxidation of alcohols by a chiral copper complex.Exchanging the substrate specificities of pyruvate decarboxylase from Zymomonas mobilis and benzoylformate decarboxylase from Pseudomonas putida.Theoretical investigation on the chemoselective N-heterocyclic carbene-catalyzed cross-benzoin reactions.Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst.Advances in chemoselective intermolecular cross-benzoin-type condensation reactions.Factors mediating activity, selectivity, and substrate specificity for the thiamin diphosphate-dependent enzymes benzaldehyde lyase and benzoylformate decarboxylase.Expedient synthesis of C-aryl carbohydrates by consecutive biocatalytic benzoin and aldol reactions.A Family of Thiazolium Salt Derived N-Heterocyclic Carbenes (NHCs) for Organocatalysis: Synthesis, Investigation and Application in Cross-Benzoin CondensationRegio- and Stereoselective Aliphatic-Aromatic Cross-Benzoin Reaction: Enzymatic Divergent CatalysisA Tailor-Made Chimeric Thiamine Diphosphate Dependent Enzyme for the Direct Asymmetric Synthesis of (S)-BenzoinsEin maßgeschneidertes chimäres Thiamindiphosphat-abhängiges Enzym zur direkten asymmetrischen Synthese von (S)-BenzoinenTailoring theS-Selectivity of 2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate Synthase (MenD) fromEscherichia coliS-Selective Mixed Carboligation by Structure-Based Design of the Pyruvate Decarboxylase from Acetobacter pasteurianus
P2860
Q26741385-5993F287-3ECA-4E0E-9257-0B5BDCC03298Q27654357-1DA34DFE-6FB6-4668-BB93-40991130E8F6Q28081119-B186B392-64D4-4A28-9FE8-FAE5EA116336Q33862899-5C114FD3-BE9A-45C1-BC27-C0E4D59AB631Q33923088-F612604E-8E34-47D9-9EF9-E043A8581A53Q34408024-079CFBA5-9157-4F54-B8BE-03F977137584Q34479601-BB473103-8C5A-468E-BD9B-6150ACCC66EDQ35869976-2A2F00CF-8E42-41E3-BF63-400D5CA3462EQ36403879-31CB31D4-94E1-4A30-9AEC-3D00BC9B2400Q37286639-F60E9D20-2F6B-4DA5-A329-533BE2171628Q37323678-A9E82B6A-B586-45ED-A5C6-E450788D94E5Q38052878-802257FC-3454-4B32-B76B-8337E8E65497Q38124949-7F02F0FE-9899-4C56-BAFA-DA607922454BQ38128203-3B4ACA75-E96B-4526-A67B-00D438D5DF65Q38137348-D2778102-5648-4636-BAB9-FBF510792524Q41818967-CB663CDA-E9A4-459F-AC2D-51FEA3F459CBQ42037810-D15B55ED-2F07-423B-B5D9-201484816230Q42285130-E4DE6256-589E-490F-9E35-B682DA459465Q42409810-1616B4EA-38C8-4925-A0A7-6BAD6DD9CF4EQ42850708-328DC712-F6EF-404A-A1D8-859714950649Q43835303-A7DFC532-517D-468F-8247-B5D6B72A410EQ46183759-C21C1C07-6D0A-4F78-A99C-1FCA694E8117Q46522364-CF54DDFD-3513-4E70-8BE9-FF6092B7659BQ46774135-786F7AF1-A493-41E7-89FD-108BDEC6AD90Q50107593-1A19CC15-7E64-4B5F-AC4A-73AA0ACA92BDQ53111213-115705AF-12FE-43E6-886F-1428806A7D7AQ53592679-74A55614-2084-43C2-86ED-6E5816C6C4E5Q54274348-612233BF-D797-4801-AB85-21222CFCB534Q57657296-9D56B641-F0F0-4ED5-B220-DF35C77E0C99Q58942531-155DC61B-0DBB-4DAB-AE96-963E3089CD0DQ58942645-B5199589-D42C-440F-8E7F-9CB8036655F7Q58942741-1B6A7D20-A2C6-43CD-8248-A66A10AA8572Q58942946-177843E9-3DE1-412A-BE35-859BC894A3A5Q58943216-537B4CF5-5F41-4309-920A-5A571AADB399
P2860
Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: the first asymmetric cross-benzoin condensation.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Development of a donor-accepto ...... ic cross-benzoin condensation.
@en
Development of a donor-accepto ...... ic cross-benzoin condensation.
@nl
type
label
Development of a donor-accepto ...... ic cross-benzoin condensation.
@en
Development of a donor-accepto ...... ic cross-benzoin condensation.
@nl
prefLabel
Development of a donor-accepto ...... ic cross-benzoin condensation.
@en
Development of a donor-accepto ...... ic cross-benzoin condensation.
@nl
P2093
P356
P1476
Development of a donor-accepto ...... ic cross-benzoin condensation.
@en
P2093
Adam Nitsche
Ayhan S Demir
Bettina Lingen
Doris Kolter-Jung
Martin Baumann
Martina Pohl
Michael Müller
Pascal Dünkelmann
Petra Siegert
P304
12084-12085
P356
10.1021/JA0271476
P407
P577
2002-10-01T00:00:00Z