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On the Mechanism of Thiamine Action. IV.1 Evidence from Studies on Model Systems
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.194402701183openalex-snapshot
Zur Kenntnis der 4‐Methylthiazol‐2‐carbonsäure
inferredcites →https://doi.org/10.1002/hlca.19480310333openalex-snapshot
Beitrag zum Problem der Decarboxylierung. 4. Mitteilung
inferredcites →https://doi.org/10.1007/978-3-642-91872-8openalex-snapshot
Die Organischen Katalysatoren und ihre Beziehungen zu den Fermenten
inferredcites →https://doi.org/10.1016/s0083-6729(08)60825-0openalex-snapshot
The Physiology of Thiamine
inferredcites →https://doi.org/10.1021/ac60065a032openalex-snapshot
Microdetermination of Deuterium in Organic Compounds
inferredcites →https://doi.org/10.1039/ct9038300995openalex-snapshot
XCVI.—Reactions involving the addition of hydrogen cyanide to carbon compounds
inferredcites →https://doi.org/10.1039/tf9433900253openalex-snapshot
Rates and equilibria in the ionisation of C–H bonds
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Redox Landscape of the 2-Oxoacid:Ferredoxin Oxidoreductase Superfamily Reveals Universally Conserved Fe–S Cluster Potentials
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Theoretical studies on the decarboxylation reaction in thiamin catalysis
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GROMOS-MD simulations on the coenzyme thiamin diphosphate in apoenzyme environment
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Synthesis and Crystal Structure of Bis(2,3-dihydro-3-methylbenzothiazole-2-ylidene)palladium(II) Diiodide: The First Palladium Complex with Benzothiazole Carbene Ligands Suitable for Homogeneous Catalysis
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Direkte Beobachtung radikalischer Zwischenstufen bei Untersuchungen zum Redoxverhalten von Modellen des Coenzyms Thiamin
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3-Benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium Chloride
inferred← citeshttps://doi.org/10.1002/047084289x.rb055.pub2openalex-snapshot
3-Benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium Chloride
inferred← citeshttps://doi.org/10.1002/047084289x.rb065openalex-snapshot
3-Benzyl-4-methyl-1,3-thiazolium Chloride
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5-(1,1-Dimethylethyl)-5,6-dihydro-2-phenyl-(5S)-oxazolo[2,3-c]-1,2,4-triazolium tetrafluoroborate
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1,3-Dimethyl-1H-Benzimidazolium Salts
inferred← citeshttps://doi.org/10.1002/047084289x.rn01925openalex-snapshot
1,2-Bis(diethylamino)cyclopropenium Tetraphenylborate
inferred← citeshttps://doi.org/10.1002/0471238961.2008090102211804.a01openalex-snapshot
Thiamine (B1)
inferred← citeshttps://doi.org/10.1002/0471264180.or040.04openalex-snapshot
The Catalyzed NucleophilicAddition of Aldehydes to Electrophilic Double Bonds
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The Catalytic Enantioselective Stetter Reaction
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Acyloin Condensation by Thiazolium Ion Catalysis: Butyroin
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Preparation of Chiral and Achiral Triazolium Salts: Carbene Precursors with Demonstrated Synthetic Utility
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Sustainable Polymers from Biomass‐Derived α‐Methylene‐γ‐Butyrolactones
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Vitamin, 6. Vitamin B 1(Thiamin)
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Asymmetrische Organokatalyse
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Ein effizienter nucleophiler Carben-Katalysator für die asymmetrische Benzoinkondensation
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Enantioselective Organocatalysis
inferred← citeshttps://doi.org/10.1002/1521-3773(20020415)41:8<1290::aid-anie1290>3.0.co;2-yopenalex-snapshot
N-Heterocyclic Carbenes: A New Concept in Organometallic Catalysis
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An Efficient Nucleophilic Carbene Catalyst for the Asymmetric Benzoin Condensation
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Nature: A Model System for Chemists
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Enzymatic C‐C Bond Formation, Asymmetric
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Biochemistry and Chemistry of Lipoic Acids
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Artificial Enzymes and Enzyme Models
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Mechanisms Related to Enzyme Catalysis
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Cyanine Dyes Derived from Thiazolium Salts
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Properties and Reactions of Thiazole
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The Nature of N‐Heterocyclic Carbenes
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A Fifty‐Year Perspective on Chemistry in Water
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Biomimicry in Organic Synthesis
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Asymmetric Protonation of Carbanions and Polar Double Bonds: Application to Total Syntheses
inferred← citeshttps://doi.org/10.1002/9781118604755.ch02openalex-snapshot
Activation Modes In Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781118604755.ch07openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed C–C Bond Formation
inferred← citeshttps://doi.org/10.1002/9781118730379.ch3openalex-snapshot
Acid–Base Chemistry of Carbenes
inferred← citeshttps://doi.org/10.1002/9781118730379.ch9openalex-snapshot
Catalytic Reactions withN‐Mesityl‐SubstitutedN‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/9781118906378.ch6openalex-snapshot
Stereoelectronic Effects with Donor and Acceptor Separated by a Single Bond Bridge
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ASYMMETRIC CARBENE CATALYSIS
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Microwave‐Assisted Solid‐Phase Synthesis
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L ewis Base– L ewis Acid Cooperative Catalysis
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The Principles of and Reasons for Using Water as a Solvent for Green Chemistry
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Synthesis in Green Solvents
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Design of Safer Chemicals – Ionic Liquids
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Designing Safer Organocatalysts – What Lessons Can Be Learned When the Rebirth of an Old Research Area Coincides with the Advent of Green Chemistry?
inferred← citeshttps://doi.org/10.1002/9783527652235.ch10openalex-snapshot
Enantioselective Annulations with Chiral N‐Mesityl N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/9783527654628.ch6openalex-snapshot
Macrocycles: From Reluctant Ring Closure to Reluctant Ring Opening
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From Catalysis to Lewis Base Catalysis with Highlights from 1806 to 1970
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Chiral Lewis Base Activation of Acyl and Related Donors in Enantioselective Transformations ( n ?→?π * )
inferred← citeshttps://doi.org/10.1002/9783527675142.ch27openalex-snapshot
Catalysis with Stable Carbenes ( n ?→?π*)
inferred← citeshttps://doi.org/10.1002/9783527809042.ch3openalex-snapshot
N‐Heterocyclic Carbene‐catalyzed S tetter Reaction and Related Chemistry
inferred← citeshttps://doi.org/10.1002/9783527809042.ch4openalex-snapshot
N‐Heterocyclic Carbene ( NHC )‐Mediated Generation and Reactions of Homoenolates
inferred← citeshttps://doi.org/10.1002/9783527809042.ch5openalex-snapshot
Domino Processes in NHC Catalysis
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Recent Activation Modes in NHC Organocatalysis
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N‐Heterocyclic Carbenes as B rønsted Base Catalysts
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Homologation Reactions with CO 2
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Organocatalytic Umpolung Strategies: Beyond Classical Reactivity Patterns
inferred← citeshttps://doi.org/10.1002/9783527832217.ch19openalex-snapshot
Computational Studies – A Useful Tool in Elucidation of Mechanisms of Organocatalytic Reactions
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Thiazolium Ylide‐Catalyzed Intramolecular Aldehyde$\rm{-}$Ketone Benzoin‐Forming Reactions: Substrate Scope
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Bredereck's Reagent Revisited: Latent Anionic Ring‐Opening Polymerization and Transesterification Reactions
inferred← citeshttps://doi.org/10.1002/adsc.200800051openalex-snapshot
Diastereoselective Synthesis of Trifluoromethylated γ‐Butyrolactones via N‐Heterocyclic Carbene‐Catalyzed Conjugated Umpolung of α,β‐Unsaturated Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.200800371openalex-snapshot
From Mono‐Triazolium Salt to Bis‐Triazolium Salt: Improvement of the Asymmetric Intermolecular Benzoin Condensation
inferred← citeshttps://doi.org/10.1002/adsc.201000240openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Reaction of Alkynyl Aldehydes with 1,3‐Keto Esters or 1,3‐Diketones
inferred← citeshttps://doi.org/10.1002/adsc.201000555openalex-snapshot
Study on the Reactivity of Aldehydes in Electrolyzed Ionic Liquids: Benzoin Condensation – Volatile Organic Compounds (VOCs) vs. Room Temperature Ionic Liquids (RTILs)
inferred← citeshttps://doi.org/10.1002/adsc.201000828openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Intramolecular Hydroacylation of Activated Alkynes: Synthesis of Chromones
inferred← citeshttps://doi.org/10.1002/adsc.201100622openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Enantioselective Annulation of Bromoenal and 1,3‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201200031openalex-snapshot
Exploiting Acyl and Enol Azolium Intermediates via N‐Hetero‐ cyclic Carbene‐Catalyzed Reactions of α‐Reducible Aldehydes
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N‐Heterocyclic Carbene‐Catalyzed Annulations of Enals and Ynals with Indolin‐3‐ones: Synthesis of 3,4‐Dihydropyrano[3,2‐b]indol‐2‐ones
inferred← citeshttps://doi.org/10.1002/adsc.201300219openalex-snapshot
Enantioselective N‐Heterocyclic Carbene‐Catalyzed Annulations of 2‐Bromoenals with 1,3‐Dicarbonyl Compounds and Enamines via Chiral α,β‐Unsaturated Acylazoliums
inferred← citeshttps://doi.org/10.1002/adsc.201300652openalex-snapshot
Methylsulfinyl (Dimsyl) Anion as Umpolung Catalyst for the Chemoselective Cross‐Benzoin Reaction of α‐Diketones with Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201300801openalex-snapshot
On the Involvement of a Spiroepoxide Intermediate in N‐Heterocyclic Carbene (NHC)‐Catalyzed Benzoin Condensations – An Approach by Oxygenation of Deoxy‐Breslow Intermediates
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Electrogenerated N‐Heterocyclic Carbene in Ionic Liquid: An Insight into the Mechanism of the Oxidative Esterification of Aromatic Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201400712openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Benzoin Strategy for Divergent Synthesis of Cyclitol Derivatives from Alditols
inferred← citeshttps://doi.org/10.1002/adsc.201400739openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Oxidative Amidation of Aldehydes with Amines
inferred← citeshttps://doi.org/10.1002/adsc.201401031openalex-snapshot
Tandem Hydroformylation/Acyloin Reaction – The Synergy of Metal Catalysis and Organocatalysis Yielding Acyloins Directly from Olefins
inferred← citeshttps://doi.org/10.1002/adsc.201701269openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Double Michael Addition: Stereoselective Synthesis of Spirofluorenes and Multisubstituted Indanes
inferred← citeshttps://doi.org/10.1002/adsc.201900699openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed β‐Indolylation of α‐Bromoenals with Indoles
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The Chemistry of Azolium‐Carboxylate Zwitterions and Related Compounds: a Survey of the Years 2009–2020
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Electrochemical Generation of N‐Heterocyclic Carbenes for Use in Synthesis and Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.202101354openalex-snapshot
Combined Photoredox and Carbene Catalysis for the Synthesis of γ‐Aryloxy Ketones
inferred← citeshttps://doi.org/10.1002/adsc.202200098openalex-snapshot
Recent Advances of Thiamine in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/adsc.202300095openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Activation of 3‐Membered Rings: Cyclopropanes, Epoxides, Azirines and Aziridines
inferred← citeshttps://doi.org/10.1002/adsc.202301333openalex-snapshot
Synthesis of 1,4‐Dihydropyridines via Addition of Furfural‐Derived Trienolates to Pyridiniums under NHC Catalysis
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NHC‐Catalyzed Synthesis of 2‐Aroylchromones and Their Application in the Synthesis of Wrightiadione Analogues
inferred← citeshttps://doi.org/10.1002/adsc.70087openalex-snapshot
Thiazolium Salts: From Thiamine to Cutting‐Edge Organocatalysts
inferred← citeshttps://doi.org/10.1002/adsc.70218openalex-snapshot
Harnessing Carbenoid Reactivity From Imidazoles and Oxiranes
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Electro‐Driven Multi‐Enzymatic Cascade Conversion of CO2 to Ethylene Glycol in Nano‐Reactor
inferred← citeshttps://doi.org/10.1002/aenm.202302876openalex-snapshot
Designing Polymer Electrolytes via Ring‐Opening Polymerization for Advanced Lithium Batteries
inferred← citeshttps://doi.org/10.1002/ajoc.201500266openalex-snapshot
N‐Heterocyclic‐Carbene‐Catalyzed Stereoselective Annulations: An Efficient Strategy for the Synthesis of Chromeno[4,3‐b]pyrrolidine Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.201700520openalex-snapshot
N‐Heterocyclic‐Carbene‐Catalyzed Reactions of Nitroalkenes: Synthesizing Important Building Blocks
inferred← citeshttps://doi.org/10.1002/ajoc.201700538openalex-snapshot
Enantioselective Reactions Catalyzed by N‐Heterocyclic Carbenes
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Base‐Promoted Metal‐/Oxidant‐Free Three‐Component Tandem Annulation: A Strategy for the Construction of 2,4,5‐Trisubstituted Thiazoles via C−N Bond Cleavage of Amidines
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Synergistic N‐Heterocyclic Carbene/Palladium‐Catalyzed Aldehyde Acylation of Allylic Amines
inferred← citeshttps://doi.org/10.1002/ajoc.201900693openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Activation of Ynals for the Construction of Functional Pyridines
inferred← citeshttps://doi.org/10.1002/ajoc.202000378openalex-snapshot
Recent Advances in Stetter Reaction and Related Chemistry: An update
inferred← citeshttps://doi.org/10.1002/ajoc.202100180openalex-snapshot
Organocatalytic Enantioselective Desymmetrization of Prochiral 2,2‐Disubstituted Cyclic 1,3‐Diones
inferred← citeshttps://doi.org/10.1002/ajoc.202100289openalex-snapshot
Recent Advances in N‐Heterocyclic Carbene Catalyzed Oxidative Cyclization for the Formation of Heterocycles
inferred← citeshttps://doi.org/10.1002/ajoc.202100445openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202300599openalex-snapshot
NHC‐Catalyzed C3‐Acylation of 2‐Oxindoles by Selective Aerobic Oxidation of Aryl Aldehydes
inferred← citeshttps://doi.org/10.1002/ajoc.202400568openalex-snapshot
Green One‐Pot Strategy for the Direct Synthesis of Benzil
inferred← citeshttps://doi.org/10.1002/ajoc.202400761openalex-snapshot
Synthetic Strategy of RITA Drug Enabled by N‐Heterocylic Carbene via 1,4‐Synthon Formation and DFT Studies**
inferred← citeshttps://doi.org/10.1002/ajoc.70243openalex-snapshot
Assessment of the Reducibility of Breslow Enolates Derived From Mesoionic Carbenes
inferred← citeshttps://doi.org/10.1002/ange.19590712406openalex-snapshot
Nachweis und Charakterisierung von Zwischenprodukten der Decarboxylierung und Oxydation von Pyruvat: „aktiviertes Pyruvat” und „aktivierter Acetaldehyd”
inferred← citeshttps://doi.org/10.1002/ange.19600720503openalex-snapshot
Untersuchungen zum Wirkungsmechanismus von Enzymen
inferred← citeshttps://doi.org/10.1002/ange.19610732202openalex-snapshot
Wirkungsmechanismus von Thiaminpyrophosphat
inferred← citeshttps://doi.org/10.1002/ange.19610732310openalex-snapshot
GDCh‐Hauptversammlung Aachen
inferred← citeshttps://doi.org/10.1002/ange.19650771007openalex-snapshot
Protonenaktivität im 1.3-Dithiolium-System
inferred← citeshttps://doi.org/10.1002/ange.19670792303openalex-snapshot
Struktur und Wirkungsweise des aktiven Zentrums der Hefe‐Pyruvat‐Decarboxylase
inferred← citeshttps://doi.org/10.1002/ange.19680802003openalex-snapshot
Reaktionen elektronenreicher Olefine
inferred← citeshttps://doi.org/10.1002/ange.19720842104openalex-snapshot
Umsetzungen von elektronenreichen Olefinen mit protonaktiven Verbindungen
inferred← citeshttps://doi.org/10.1002/ange.19740861606openalex-snapshot
Addition aliphatischer Aldehyde an aktivierte Doppelbindungen
inferred← citeshttps://doi.org/10.1002/ange.19750871704openalex-snapshot
Der Pyruvatdehydrogenase-Multienzymkomplex
inferred← citeshttps://doi.org/10.1002/ange.19760882103openalex-snapshot
Die katalysierte Addition von Aldehyden an aktivierte Doppelbindungen – Ein neues Syntheseprinzip
inferred← citeshttps://doi.org/10.1002/ange.19860981227openalex-snapshot
Synthese eines makrobicyclischen Thiazolium-Wirts und supramolekulare Katalyse der Benzoinkondensation
inferred← citeshttps://doi.org/10.1002/ange.19881000106openalex-snapshot
Vitamin B12: Experimente zur Frage nach dem Ursprung seiner molekularen Struktur
inferred← citeshttps://doi.org/10.1002/ange.19881000307openalex-snapshot
Cyclophane zur Komplexierung von Neutralmolekülen
inferred← citeshttps://doi.org/10.1002/ange.19951070420openalex-snapshot
Struktur des dimeren (4‐tert‐Butyl‐thiazolato)(glyme)lithiums: Carben‐Charakter eines Formyl‐Anion‐Äquivalents
inferred← citeshttps://doi.org/10.1002/ange.19961081218openalex-snapshot
Ein Flavo‐Thiazolio‐Cyclophan als funktionsfähiges Modell für die Pyruvat‐Oxidase
inferred← citeshttps://doi.org/10.1002/ange.200301714openalex-snapshot
N‐heterocyclische Carbene: nicht nur Liganden, auch Reagentien!
inferred← citeshttps://doi.org/10.1002/ange.200461572openalex-snapshot
Organokatalysierte konjugierte Umpolung von α,β‐ungesättigten Aldehyden zur Synthese von γ‐Butyrolactonen
inferred← citeshttps://doi.org/10.1002/ange.200500723openalex-snapshot
Latent, Thermally Activated Organic Catalysts for the On‐Demand Living Polymerization of Lactide
inferred← citeshttps://doi.org/10.1002/ange.200500761openalex-snapshot
Neue Entwicklungen in der asymmetrischen Stetter‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.200502617openalex-snapshot
Erweiterte Reaktionswege im Mechanismus der Heterazolium‐Katalyse – aussichtsreiche Konzepte für vielseitige Synthesemethoden
inferred← citeshttps://doi.org/10.1002/ange.200503885openalex-snapshot
Asymmetric Intramolecular Crossed‐Benzoin Reactions by N‐Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200590041openalex-snapshot
N‐heterocyclische Carbene: nicht nur Liganden, auch Reagentien!
inferred← citeshttps://doi.org/10.1002/ange.200600268openalex-snapshot
Catalytic Enantioselective Crossed Aldehyde–Ketone Benzoin Cyclization
inferred← citeshttps://doi.org/10.1002/ange.200602701openalex-snapshot
Isolation of Cyclopropenylidene–Lithium Adducts: The Weiss–Yoshida Reagent
inferred← citeshttps://doi.org/10.1002/ange.200602836openalex-snapshot
A Ring‐Expansion Methodology Involving Multicomponent Reactions: Highly Efficient Access to Polysubstituted Furan‐Fused 1,4‐Thiazepine Derivatives
inferred← citeshttps://doi.org/10.1002/ange.200603380openalex-snapshot
N‐heterocyclische Carbene als Organokatalysatoren
inferred← citeshttps://doi.org/10.1002/ange.200604943openalex-snapshot
Lewis‐Base‐Katalyse in der organischen Synthese
inferred← citeshttps://doi.org/10.1002/ange.200703883openalex-snapshot
Heterocyclische Carbene – Synthese und Koordinationschemie
inferred← citeshttps://doi.org/10.1002/ange.200802735openalex-snapshot
Biomimetische Carben‐katalysierte Oxidation von Aldehyden mit TEMPO
inferred← citeshttps://doi.org/10.1002/ange.200907275openalex-snapshot
Umpolung von Aldehyden mit N‐heterocyclischen Carbenen: NMR‐Charakterisierung des Breslow‐Intermediats in seiner Ketoform und eines Spirodioxolans als “resting state” des katalytischen Systems
inferred← citeshttps://doi.org/10.1002/ange.201000165openalex-snapshot
Stabile cyclische Carbene und verwandte Spezies jenseits der Diaminocarbene
inferred← citeshttps://doi.org/10.1002/ange.201001658openalex-snapshot
Die Anfänge der N‐heterocyclischen Carbene
inferred← citeshttps://doi.org/10.1002/ange.201001865openalex-snapshot
Das Maß aller Ringe – N‐heterocyclische Carbene
inferred← citeshttps://doi.org/10.1002/ange.201005490openalex-snapshot
Eine intermolekulare, durch N‐heterocyclische Carbene katalysierte Hydroacylierung von Arinen
inferred← citeshttps://doi.org/10.1002/ange.201006548openalex-snapshot
Hoch enantioselektive Synthese von α‐Aminosäurederivaten durch NHC‐katalysierte intermolekulare Stetter‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.201102027openalex-snapshot
Konformative Fluoreffekte in der Organokatalyse: eine neuartige Strategie zum molekularen Design
inferred← citeshttps://doi.org/10.1002/ange.201102435openalex-snapshot
N‐Heterocyclische Carbene: Organokatalysatoren mit mäßiger Nucleophilie, aber außerordentlich hoher Lewis‐Basizität
inferred← citeshttps://doi.org/10.1002/ange.201102920openalex-snapshot
Organokatalytische Hydroacylierung nichtaktivierter Alkene
inferred← citeshttps://doi.org/10.1002/ange.201103360openalex-snapshot
Cyclopropyl Iminium Activation: Reactivity Umpolung in Enantioselective Organocatalytic Reaction Design
inferred← citeshttps://doi.org/10.1002/ange.201103555openalex-snapshot
Durch ein N‐heterocyclisches Carben katalysierte Umpolung von Michael‐Akzeptoren für intermolekulare Reaktionen
inferred← citeshttps://doi.org/10.1002/ange.201106155openalex-snapshot
Entwicklung N‐heterocyclischer Carbene: Gleichzeitige Verbesserung von Reaktivität und Enantioselektivität in der asymmetrischen Hydroacylierung von Cyclopropenen
inferred← citeshttps://doi.org/10.1002/ange.201108019openalex-snapshot
Conjugate‐Addition Organopolymerization: Rapid Production of Acrylic Bioplastics by N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/ange.201202327openalex-snapshot
Nucleophile Reaktivitäten von Desoxy‐Breslow‐Intermediaten: Wie beeinflusst Aromatizität die katalytische Aktivität N‐heterocyclischer Carbene?
inferred← citeshttps://doi.org/10.1002/ange.201204524openalex-snapshot
Struktur und Reaktivität O‐methylierter Breslow‐Intermediate
inferred← citeshttps://doi.org/10.1002/ange.201205878openalex-snapshot
Umpolung mit N‐heterocyclischen Carbenen: Generierung und Reaktivität von Breslow‐Intermediaten (2,2‐Diaminoenole)
inferred← citeshttps://doi.org/10.1002/ange.201206632openalex-snapshot
Accelerated CarbonCarbon Bond‐Forming Reactions in Preparative Electrospray
inferred← citeshttps://doi.org/10.1002/ange.201301304openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalyzed Aza‐Benzoin Reaction of Enals with Activated Ketimines
inferred← citeshttps://doi.org/10.1002/ange.201301849openalex-snapshot
An Efficient Approach to the Securinega Alkaloids Empowered by Cooperative N‐Heterocyclic Carbene/Lewis Acid Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201303107openalex-snapshot
Charakterisierung der Schlüsselintermediate von carbenkatalysierten Umpolungen durch Kristallstrukturanalyse/NMR‐Spektroskopie: Breslow‐Intermediate, Homoenolate und Azoliumenolate
inferred← citeshttps://doi.org/10.1002/ange.201307167openalex-snapshot
Bis(amino)cyclopropenylidenes as Organocatalysts for Acyl Anion and Extended Umpolung Reactions
inferred← citeshttps://doi.org/10.1002/ange.201406630openalex-snapshot
Proton‐Transfer Polymerization (HTP): Converting Methacrylates to Polyesters by an N‐Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1002/ange.201406865openalex-snapshot
Diversity‐Oriented Synthesis of Drug‐Like Macrocyclic Scaffolds Using an Orthogonal Organo‐ and Metal Catalysis Strategy
inferred← citeshttps://doi.org/10.1002/ange.201407469openalex-snapshot
N‐Heterocyclic Carbene Catalyzed Cyclocondensation of α,β‐Unsaturated Carboxylic Acids: Enantioselective Synthesis of Pyrrolidinone and Dihydropyridinone Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201409004openalex-snapshot
Dekonstruktion kovalenter Organokatalyse
inferred← citeshttps://doi.org/10.1002/ange.201501840openalex-snapshot
Rate and Equilibrium Constants for the Addition of N‐Heterocyclic Carbenes into Benzaldehydes: A Remarkable 2‐Substituent Effect
inferred← citeshttps://doi.org/10.1002/ange.201507802openalex-snapshot
Enantioselective Synthesis of Spirocyclohexadienones by NHC‐Catalyzed Formal [3+3] Annulation Reaction of Enals
inferred← citeshttps://doi.org/10.1002/ange.201508368openalex-snapshot
Radical [1,3] Rearrangements of Breslow Intermediates
inferred← citeshttps://doi.org/10.1002/ange.201605319openalex-snapshot
Kooperative Katalyse mit N‐heterocyclischen Carbenen
inferred← citeshttps://doi.org/10.1002/ange.201605979openalex-snapshot
Vermittlung organischer Reaktionen durch nichtbenzoide carbocyclische aromatische Ionen
inferred← citeshttps://doi.org/10.1002/ange.201611268openalex-snapshot
N‐Heterocyclic‐Carbene‐Catalyzed Umpolung of Imines
inferred← citeshttps://doi.org/10.1002/ange.201700059openalex-snapshot
Carbonyls as Latent Alkyl Carbanions for Conjugate Additions
inferred← citeshttps://doi.org/10.1002/ange.201701485openalex-snapshot
Durch N‐heterocyclische Carbene katalysierte oxidative Dearomatisierung von Indolen zu spirocyclischen Indoleninen mit quartärem Stereozentrum
inferred← citeshttps://doi.org/10.1002/ange.201702148openalex-snapshot
Cyclische Alkylaminocarbene (CAACs): Neues von guten Bekannten
inferred← citeshttps://doi.org/10.1002/ange.201708305openalex-snapshot
Treten in der N‐heterozyklischen Carben‐Organokatalyse wirklich Carbene auf?
inferred← citeshttps://doi.org/10.1002/ange.201709684openalex-snapshot
Katalyse durch N‐heterocyclische Carbene über Azoliumdienolate: eine effiziente Strategie für enantioselektive Funktionalisierungen an entfernten Positionen
inferred← citeshttps://doi.org/10.1002/ange.201709802openalex-snapshot
Triazaphospholenium‐tetrafluoroborat: das Phosphoranalogon eines von 1,2,3‐Triazol abgeleiteten Carbens
inferred← citeshttps://doi.org/10.1002/ange.201712732openalex-snapshot
Moderne Aspekte der Elektrochemie zur Synthese hochwertiger organischer Produkte
inferred← citeshttps://doi.org/10.1002/ange.201712785openalex-snapshot
Catalytic Enantioselective Aza‐Benzoin Reactions of Aldehydes with 2H‐Azirines
inferred← citeshttps://doi.org/10.1002/ange.201712811openalex-snapshot
Synergistic N‐Heterocyclic Carbene/Palladium‐Catalyzed Reactions of Aldehyde Acyl Anions with either Diarylmethyl or Allylic Carbonates
inferred← citeshttps://doi.org/10.1002/ange.201801676openalex-snapshot
Breslow‐Intermediate aromatischer N‐heterocyclischer Carbene (Benzimidazolin‐2‐ylidene, Thiazolin‐2‐ylidene)
inferred← citeshttps://doi.org/10.1002/ange.201804271openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalyzed Cyclopentene Synthesis via the β‐Azolium Ylide
inferred← citeshttps://doi.org/10.1002/ange.201806569openalex-snapshot
Umpolung Reactivity of Aldehydes toward Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/ange.201904308openalex-snapshot
Breslow Intermediates from a Thiazolin‐2‐ylidene and Fluorinated Aldehydes: XRD and Solution‐Phase NMR Spectroscopic Characterization
inferred← citeshttps://doi.org/10.1002/ange.201909017openalex-snapshot
Visible‐Light‐Driven N‐Heterocyclic Carbene Catalyzed γ‐ and ϵ‐Alkylation with Alkyl Radicals
inferred← citeshttps://doi.org/10.1002/ange.201910350openalex-snapshot
Cyclic (Aryl)(Amido)Carbenes: NHCs with Triplet‐like Reactivity
inferred← citeshttps://doi.org/10.1002/ange.202001824openalex-snapshot
Combined Photoredox and Carbene Catalysis for the Synthesis of Ketones from Carboxylic Acids**
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