Highly enantioselective catalytic acyl-pictet-spengler reactions.
about
Resolution of praziquantelEnantioselective thiourea-catalyzed cationic polycyclizationsStrictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzymeAttractive noncovalent interactions in asymmetric catalysis: links between enzymes and small molecule catalystsFrom Heteroaromatic Acids and Imines to Azaspirocycles: Stereoselective Synthesis and 3D Shape AnalysisInfluence of the substitution and conformation of C--H-bond-based bis-triazole acceptors in anion-binding catalysis.Structural optimization of thiourea-based bifunctional organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones.Total synthesis of enantiopure phalarine via a stereospecific Pictet-Spengler reaction: traceless transfer of chirality from L-tryptophan.Monitoring on-chip Pictet-Spengler reactions by integrated analytical separation and label-free time-resolved fluorescence.Asymmetric Mannich synthesis of α-amino esters by anion-binding catalysis.Electronically Rich N-Substituted Tetrahydroisoquinoline 3-Carboxylic Acid Esters: Concise Synthesis and Conformational StudiesEnantioselective thiourea-catalyzed additions to oxocarbenium ions.Ruthenium-catalyzed γ-carbolinium ion formation from aryl azides; synthesis of dimebolin.Mechanism of amido-thiourea catalyzed enantioselective imine hydrocyanation: transition state stabilization via multiple non-covalent interactions.Asymmetric Friedel-crafts reaction of indoles with imines by an organic catalyst.Enantioselective Pictet-Spengler Reactions of Isatins for the Synthesis of SpiroindolonesDiastereoselective and enantioselective synthesis of tertiary alpha-hydroxy phosphonates through hydrogen-bond catalysis.Rh(II)2-catalyzed synthesis of α-, β-, or δ-carbolines from aryl azides.Catalytic stereoselective synthesis of diverse oxindoles and spirooxindoles from isatins.Acid-promoted cyclization reactions of tetrahydroindolinones. Model studies for possible application in a synthesis of selaginoidine.Mild and efficient cyanuric chloride catalyzed Pictet-Spengler reactionBroader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation.Natural products as inspiration for the development of asymmetric catalysis.Direct modification of the proinflammatory cytokine macrophage migration inhibitory factor by dietary isothiocyanatesAsymmetric ion-pairing catalysis.Asymmetric counteranion-directed catalysis: concept, definition, and applications.Enantioselective reactions of N-acyliminium ions using chiral organocatalysts.Thiourea-catalyzed enantioselective cyanosilylation of ketones.Mg(II) -Catalyzed Desymmetrization Reaction of meso-Aziridines with Hydroxylamines: Synthesis of Novel Chiral 1,2-Diamine Skeletons.Thiourea-catalyzed enantioselective iso-Pictet-Spengler reactions.1,2,3,-Triazole-Based Catalysts: From Metal- to Supramolecular Organic Catalysis.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.Tertiary aminourea-catalyzed enantioselective iodolactonization.Enantioselective catalytic alpha-alkylation of aldehydes via an SN1 pathway.Biocatalytic production of tetrahydroisoquinolines.Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis.Weak Brønsted acid-thiourea co-catalysis: enantioselective, catalytic protio-Pictet-Spengler reactions.Study of the cis to trans isomerization of 1-phenyl-2,3-disubstituted tetrahydro-beta-carbolines at C(1). Evidence for the carbocation-mediated mechanism.Biocatalytic asymmetric formation of tetrahydro-β-carbolines.Mechanistic studies on the cis to trans epimerization of trisubstituted 1,2,3,4-tetrahydro-beta-carbolines.
P2860
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P2860
Highly enantioselective catalytic acyl-pictet-spengler reactions.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@en
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@nl
type
label
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@en
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@nl
prefLabel
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@en
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@nl
P356
P1476
Highly enantioselective catalytic acyl-pictet-spengler reactions.
@en
P2093
Eric N Jacobsen
Mark S Taylor
P304
10558-10559
P356
10.1021/JA046259P
P407
P577
2004-09-01T00:00:00Z