An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
about
Organocatalytic Reactions Enabled by N-Heterocyclic CarbenesLanthanum tricyanide-catalyzed acyl silane-ketone benzoin additions and kinetic resolution of resultant alpha-silyloxyketones.Amine-linked N-heterocyclic carbenes: the importance of an pendant free-amine auxiliary in assisting the catalytic reaction.The Catalytic Asymmetric Intramolecular Stetter Reaction.Designing N-heterocyclic carbenes: simultaneous enhancement of reactivity and enantioselectivity in the asymmetric hydroacylation of cyclopropenes.2,5-Diphenyl-2,5,6,8-tetra-hydro-1,2,4-triazolo[3,4-c][1,4]oxazin-4-ium hexa-fluorido-phosphateDiscovering New Reactions with N-Heterocyclic Carbene Catalysis.Dynamic kinetic asymmetric cross-benzoin additions of β-stereogenic α-keto esters.Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes.Carbon-carbon bond activation of cyclobutenones enabled by the addition of chiral organocatalyst to ketoneQuantum mechanical investigations of organocatalysis: mechanisms, reactivities, and selectivities.Late-stage diversification of chiral N-heterocyclic-carbene precatalysts for enantioselective homoenolate additions.Diversity-oriented synthesis of drug-like macrocyclic scaffolds using an orthogonal organo- and metal catalysis strategy.The RuO4-catalysed dihydroxylation, ketohydroxylation and mono oxidation--novel oxidation reactions for the synthesis of diols and alpha-hydroxy ketones.Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: bench stable precursors for N-heterocyclic carbenes.Ligand controlled highly regio- and enantioselective synthesis of alpha-acyloxyketones by palladium-catalyzed allylic alkylation of 1,2-enediol carbonatesCarbene catalystsLanthanum tricyanide-catalyzed acyl silane-ketone benzoin additions.Computational predictions of stereochemistry in asymmetric thiazolium- and triazolium-catalyzed benzoin condensations.A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis.Lithium phosphonate umpolung catalysts: Do fluoro substituents increase the catalytic activity?Hydrazones as Singular Reagents in Asymmetric Organocatalysis.Organocatalytic upgrading of furfural and 5-hydroxymethyl furfural to C10 and C12 furoins with quantitative yield and atom-efficiency.Finding Furfural Hydrogenation Catalysts via Predictive Modelling.Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity.Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups.Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to gamma-lactams.N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones.N-Heterocyclic Carbene-Promoted Rauhut]Currier Reactions between Vinyl Sulfones and α,β-Unsaturated Aldehydes.NHC-catalyzed/titanium(IV)-mediated highly diastereo- and enantioselective dimerization of enals.N-heterocyclic-carbene-catalyzed one-pot synthesis of hydroxamic esters.Asymmetric esterification of ketenes catalyzed by an N-heterocyclic carbene.Galactose oxidase model: biomimetic enantiomer-differentiating oxidation of alcohols by a chiral copper complex.Imidazol-2-and-4-ylidene by decarboxylation. Studies on the cross-conjugated mesomeric betaine-alkaloid norzooanemonine and its pseudo-cross-conjugated isomer.Organocatalytic Highly Regio- and Enantioselective Umpolung Michael Addition Reaction of α-Imino Esters.Cycloadduct formation of α,β-unsaturated esters with azides catalyzed by NHC systems.Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst.Oxidative N-Heterocyclic Carbene-Catalyzed γ-Carbon Addition of Enals to Imines: Mechanistic Studies and Access to Antimicrobial Compounds.A NHC-catalyzed 1,3-dipolar cycloaddition reaction of allyl ketones with azides: direct access to 1,4,5-trisubstituted 1,2,3-triazoles.
P2860
Q28081119-DE3E524F-1F14-4DB2-B93D-87F7A58C607CQ33862899-AADB2D5C-6072-42F9-8970-253C298EEB50Q33875441-4EDD7B2F-3C5D-40B5-9DBE-D5700DE1D338Q33923088-69DA1BFF-7235-4D0E-91F8-5C6B628B6128Q34068393-36519776-1D84-4D88-AD3D-61212E259E90Q34230950-D89C5ACD-6A45-49CF-A1CD-18D535E34346Q34284871-171EE52C-A4EB-4A2D-873F-EC21123F39A3Q34408024-AEFF2EE9-2B08-45BA-8E7E-26A43D008C40Q34463867-F38957C7-20C3-4660-815B-3DDBCC0B631AQ35081968-0E09D644-47D3-42F6-AAAB-F10B27175350Q35159601-7BB14433-4F0B-4985-BD89-8EC958B9D976Q35231395-70A9013D-5830-4327-A425-AF41F5E54BFCQ35278303-9DDF58A0-24AD-461C-83B1-9EF7D75219C5Q35869976-6260180C-9DEE-474A-886E-B5184B6C13E3Q35981088-D8727E90-FCDA-4255-B04B-DC81C50BE3B7Q36856995-CC6705B7-A843-450D-B375-F50B7E4C282AQ37263857-9E3ADBB7-9EE3-441B-9681-31E131EFAC2FQ37286639-9ADA756A-4F2F-49DC-85B7-CEA411497522Q37323678-6E291AE9-F263-4C2D-B332-3AC2E297E512Q37649146-B8B065BA-DCC4-4895-8404-83733A30B9B5Q38052878-29929397-BF93-4D84-95D5-5588FE97BA05Q38586540-ADD1C934-47E6-461F-B009-CB5EB070872EQ38934959-0CED0E68-76A2-4F53-8083-FEB015E3C247Q40455491-474FC277-1371-4371-803D-3F58B81FF2E4Q41518831-887C1EAC-8AE3-49CA-82AF-63B78F9ABC12Q41904191-29004AC6-0AE8-489B-900F-32DB981DCC45Q42292940-A9990AD4-1158-439D-A89C-C053A3A7E234Q42483535-D8E8BB4B-CDC3-4F3C-8D9A-989A5AEAEE52Q42574353-109C98EF-BC2A-4C71-BD08-B33A014F8CE0Q42607555-1927A0BC-D328-49BB-87CD-4B19352A0CA4Q42636978-E8436534-876E-40E5-87D2-012BFBC1DC56Q43835303-8A50DB9C-96A5-43AB-9DC0-C34536960990Q46182875-E5A0C63A-F118-4BDD-857B-758FCB93B843Q46183759-85F0CAB0-59AF-4698-82E2-77F7D1CDC627Q46823456-08912A56-8B8C-4268-9897-B3FD224D4E1AQ47810000-4D396A68-ED01-400E-A701-E855889A60D3Q48618375-09349CAC-66B5-4801-8009-32EC6D5638E3Q50107593-6B573795-9791-4CA4-8B22-5F21573D9083Q50270857-F3928D31-7C78-441C-A161-634ADE420A60Q50645803-D121E23E-6A7A-4DAF-BD95-737E31FF49F2
P2860
An efficient nucleophilic carbene catalyst for the asymmetric 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
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@en
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@nl
type
label
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@en
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@nl
prefLabel
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@en
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@nl
P1433
P1476
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
@en
P2093
Dieter Enders
Ulrike Kallfass
P2860
P304
P356
10.1002/1521-3773(20020517)41:10<1743::AID-ANIE1743>3.0.CO;2-Q
P577
2002-05-01T00:00:00Z