On the public citation graph
Highly Enantioselective Benzoin Condensation Reactions Involving a Bifunctional Protic Pentafluorophenyl-Substituted Triazolium Precatalyst
0 signed · 197 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020517)41:10<1743::aid-anie1743>3.0.co;2-qopenalex-snapshot
An Efficient Nucleophilic Carbene Catalyst for the Asymmetric Benzoin Condensation
inferredcites →https://doi.org/10.1002/adsc.200800371openalex-snapshot
From Mono‐Triazolium Salt to Bis‐Triazolium Salt: Improvement of the Asymmetric Intermolecular Benzoin Condensation
inferredcites →https://doi.org/10.1002/adsc.200800532openalex-snapshot
Asymmetric Dimerization of Disubstituted Ketenes Catalyzed by N‐Heterocyclic Carbenes
inferredcites →https://doi.org/10.1002/anie.200301702openalex-snapshot
Catalyzed Reactions of Acyl Anion Equivalents
inferredcites →https://doi.org/10.1002/anie.200500761openalex-snapshot
New Developments in the Asymmetric Stetter Reaction
inferredcites →https://doi.org/10.1002/anie.200502617openalex-snapshot
Extending Mechanistic Routes in Heterazolium Catalysis–Promising Concepts for Versatile Synthetic Methods
inferredcites →https://doi.org/10.1002/anie.200603380openalex-snapshot
N‐Heterocyclic Carbenes as Organocatalysts
inferredcites →https://doi.org/10.1002/chem.200900532openalex-snapshot
The First Magnetic Nanoparticle‐Supported Chiral DMAP Analogue: Highly Enantioselective Acylation and Excellent Recyclability
inferredcites →https://doi.org/10.1002/ejoc.200300762openalex-snapshot
Preparation of Axially Chiral N,N′‐Diarylimidazolium and N‐Arylthiazolium Salts and Evaluation of Their Catalytic Potential in the Benzoin and in the Intramolecular Stetter Reactions
inferredcites →https://doi.org/10.1002/hlca.19960790427openalex-snapshot
A Novel Asymmetric Benzoin Reaction Catalyzed by a Chiral Triazolium Salt. Preliminary communication
inferredcites →https://doi.org/10.1002/jlac.18320030302openalex-snapshot
Untersuchungen über das Radikal der Benzoesäure
inferredcites →https://doi.org/10.1016/0040-4039(93)85117-fopenalex-snapshot
Introduction to a rational design of chiral thiazolium salts
inferredcites →https://doi.org/10.1016/j.tetasy.2008.05.017openalex-snapshot
Synthesis of enantiopure triazolium salts from pyroglutamic acid and their evaluation in the benzoin condensation
inferredcites →https://doi.org/10.1016/s0040-4039(97)00681-3openalex-snapshot
Synthesis of and asymmetric induction by chiral bicyclic thiazolium salts
inferredcites →https://doi.org/10.1016/s0040-4039(97)00682-5openalex-snapshot
Synthesis of and asymmetric induction by chiral polycyclic thiazolium salts
inferredcites →https://doi.org/10.1016/s0040-4039(98)00439-0openalex-snapshot
Catalysis of benzoin condensation by conformationally-restricted chiral bicyclic thiazolium salts
inferredcites →https://doi.org/10.1021/ar030050jopenalex-snapshot
Nucleophilic Carbenes in Asymmetric Organocatalysis
inferredcites →https://doi.org/10.1021/cr068372zopenalex-snapshot
Organocatalysis by N-Heterocyclic Carbenes
inferredcites →https://doi.org/10.1021/ja039461lopenalex-snapshot
Asymmetric Benzoin Condensation Catalyzed by Chiral Rotaxanes Tethering a Thiazolium Salt Moiety via the Cooperation of the Component: Can Rotaxane Be an Effective Reaction Field?
inferredcites →https://doi.org/10.1021/ja042650zopenalex-snapshot
Thiazolylalanine-Derived Catalysts for Enantioselective Intermolecular Aldehyde−Imine Cross-Couplings
inferredcites →https://doi.org/10.1021/jo00923a006openalex-snapshot
Asymmetric thiazolium salt catalysis of the benzoin condensation
inferredcites →https://doi.org/10.1021/jo050645nopenalex-snapshot
An Efficient Synthesis of Achiral and Chiral 1,2,4-Triazolium Salts: Bench Stable Precursors for N-Heterocyclic Carbenes
inferredcites →https://doi.org/10.1021/jo071223bopenalex-snapshot
Nonenzymatic Acylative Kinetic Resolution of Baylis−Hillman Adducts
inferredcites →https://doi.org/10.1021/ol070929popenalex-snapshot
Modified Chiral Triazolium Salts for Enantioselective Benzoin Cyclization of Enolizable Keto-Aldehydes: Synthesis of (+)-Sappanone B
inferredcites →https://doi.org/10.1021/ol702759bopenalex-snapshot
Chiral N-Heterocyclic Carbene Catalyzed Staudinger Reaction of Ketenes with Imines: Highly Enantioselective Synthesis of N-Boc β-Lactams
inferredcites →https://doi.org/10.1039/a803635gopenalex-snapshot
Comparison of chiral thiazolium and triazolium salts as asymmetric catalysts for the benzoin condensation
inferredcites →https://doi.org/10.1039/b414574gopenalex-snapshot
A peptide-catalyzed asymmetric Stetter reaction
inferredcites →https://doi.org/10.1039/b419335kopenalex-snapshot
Kinetic resolution of sec-alcohols using a new class of readily assembled (S)-proline-derived 4-(pyrrolidino)-pyridine analogues
inferredcites →https://doi.org/10.1039/b604632kopenalex-snapshot
Asymmetric acyl-transfer promoted by readily assembled chiral 4-N,N-dialkylaminopyridine derivatives
inferredcites →https://doi.org/10.1039/b806816jopenalex-snapshot
Tandem multi-step synthesis of C-carboxyazlactones promoted by N-heterocyclic carbenes
inferredcites →https://doi.org/10.1039/b908517copenalex-snapshot
The enantioselective benzoin condensation promoted by chiral triazolium precatalysts: stereochemical control via hydrogen bonding
inferredcites →https://doi.org/10.1246/bcsj.53.478openalex-snapshot
Asymmetric Benzoin Condensation Catalyzed by Optically Active Thiazolium Salts in Micellar Two-phase Media
inferredcites →https://doi.org/10.1246/cl.2008.2openalex-snapshot
Development of Chiral Bicyclic Triazolium Salt Organic Catalysts: The Importance of the N-Aryl Substituent
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4781817openalex-extracted
Enhancing the Hydrophilicity of Covalent Organic Polymers by Self-Condensation for Photocatalytic Hydrogen Generation with Unprecedented Apparent Quantum Yield Up to 500 Nm
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub4openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub5openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub6openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9781118604755.ch07openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed C–C Bond Formation
inferred← citeshttps://doi.org/10.1002/9781118662083.cot08-005openalex-snapshot
Formation of Aldehydes and Ketones by Condensation Reactions
inferred← citeshttps://doi.org/10.1002/9781119972471.ch1openalex-snapshot
Reactions of Aldehydes and Ketones and their Derivatives
inferred← citeshttps://doi.org/10.1002/9783527675142.ch27openalex-snapshot
Catalysis with Stable Carbenes ( n ?→?π*)
inferred← citeshttps://doi.org/10.1002/9783527809042.ch12openalex-snapshot
N‐Heterocyclic Carbene Catalysis in Natural Product and Complex Target Synthesis
inferred← citeshttps://doi.org/10.1002/9783527832217.ch15openalex-snapshot
Organocatalytic Umpolung Strategies: Beyond Classical Reactivity Patterns
inferred← citeshttps://doi.org/10.1002/adsc.201000187openalex-snapshot
Enantioselective Synthesis of Spirocyclic Oxindole‐β‐lactones via N‐Heterocyclic Carbene‐Catalyzed Cycloaddition of Ketenes and Isatins
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.201200499openalex-snapshot
Construction of Contiguous Tetrasubstituted Carbon Stereocenters by Intramolecular Crossed Benzoin Reactions Catalyzed by N‐Heterocyclic Carbene (NHC) Organocatalyst
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.202100186openalex-snapshot
Visible Light Enabled Formal Cross Silyl Benzoin Reaction as an Access to α‐Hydroxyketones
inferred← citeshttps://doi.org/10.1002/adsc.70087openalex-snapshot
Thiazolium Salts: From Thiamine to Cutting‐Edge Organocatalysts
inferred← citeshttps://doi.org/10.1002/ange.201105127openalex-snapshot
Die Diaryl(oxy)methyl‐Gruppe: mehr als ein unbeteiligter Zuschauer in chiralen Auxiliaren, Katalysatoren und Dotierstoffen
inferred← citeshttps://doi.org/10.1002/ange.201203704openalex-snapshot
Anwendungen der Katalyse mit N‐heterocyclischen Carbenen in Totalsynthesen
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.201303903openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [4+3] Annulation of Enals and o‐Quinone Methides: Highly Enantioselective Synthesis of Benzo‐ε‐Lactones
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.201612462openalex-snapshot
Enantioselektive Chemo‐ und Biokatalyse: Partner in der Retrosynthese
inferred← citeshttps://doi.org/10.1002/ange.7124073openalex-snapshot
Cyclobenzoin Macrocycles: Guest Capture and Applications in Energy Technologies
inferred← citeshttps://doi.org/10.1002/anie.201105127openalex-snapshot
The Diaryl(oxy)methyl Group: More than an Innocent Bystander in Chiral Auxiliaries, Catalysts, and Dopants
inferred← citeshttps://doi.org/10.1002/anie.201203704openalex-snapshot
A Continuum of Progress: Applications of N‐Hetereocyclic Carbene Catalysis in Total Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201301304openalex-snapshot
Enantioselective N‐Heterocyclic Carbene Catalyzed Aza‐Benzoin Reaction of Enals with Activated Ketimines
inferred← citeshttps://doi.org/10.1002/anie.201303903openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [4+3] Annulation of Enals and o ‐Quinone Methides: Highly Enantioselective Synthesis of Benzo‐ε‐Lactones
inferred← citeshttps://doi.org/10.1002/anie.201406865openalex-snapshot
Diversity‐Oriented Synthesis of Drug‐Like Macrocyclic Scaffolds Using an Orthogonal Organo‐ and Metal Catalysis Strategy
inferred← citeshttps://doi.org/10.1002/anie.201612462openalex-snapshot
Enantioselective Chemo‐ and Biocatalysis: Partners in Retrosynthesis
inferred← citeshttps://doi.org/10.1002/anie.7124073openalex-snapshot
Cyclobenzoin Macrocycles: Guest Capture and Applications in Energy Technologies
inferred← citeshttps://doi.org/10.1002/asia.201000829openalex-snapshot
Amine‐Linked N‐Heterocyclic Carbenes: The Importance of an Pendant Free‐Amine Auxiliary in Assisting the Catalytic Reaction
inferred← citeshttps://doi.org/10.1002/cctc.201100218openalex-snapshot
Enantiopure Triazolium Salts: Chemoenzymatic Synthesis and Applications in Organocatalysis
inferred← citeshttps://doi.org/10.1002/cctc.202001513openalex-snapshot
Bifunctional N‐Heterocylic Carbene‐Catalyzed Highly Enantioselective Trans‐Cyclopentannulation of Enals and Enones via Homoenolate
inferred← citeshttps://doi.org/10.1002/cctc.202401078openalex-snapshot
Improvement of Asymmetric Reactions via Remote Electronic Tuning of N‐Heterocyclic Carbene Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201201375openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Homoenolate Additions with N‐Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic γ‐Lactam Oxindoles
inferred← citeshttps://doi.org/10.1002/chem.201204386openalex-snapshot
N‐Heterocyclic Carbene (NHC)‐Catalyzed/Lewis Acid Mediated Conjugate Umpolung of Alkynyl Aldehydes for the Synthesis of Butenolides: A Formal [3+2] Annulation
inferred← citeshttps://doi.org/10.1002/chem.201405828openalex-snapshot
Bifunctional N‐Heterocyclic Carbene Catalyzed [3+4] Annulation of Enals and Aurones
inferred← citeshttps://doi.org/10.1002/chem.201503851openalex-snapshot
Cyclotetrabenzoin: Facile Synthesis of a Shape‐Persistent Molecular Square and Its Assembly into Hydrogen‐Bonded Nanotubes
inferred← citeshttps://doi.org/10.1002/chem.202300858openalex-snapshot
Remote Electronic Effect of Chiral N‐Heterocyclic Carbene Catalyst on an Asymmetric Benzoin Reaction
inferred← citeshttps://doi.org/10.1002/chin.201017091openalex-snapshot
ChemInform Abstract: Highly Enantioselective Benzoin Condensation Reactions Involving a Bifunctional Protic Pentafluorophenyl‐Substituted Triazolium Precatalyst.
inferred← citeshttps://doi.org/10.1002/cjoc.202000107openalex-snapshot
N‐Heterocyclic Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates
inferred← citeshttps://doi.org/10.1002/cssc.202102157openalex-snapshot
Mechanochemical Organocatalysis: Do High Enantioselectivities Contradict What We Might Expect?
inferred← citeshttps://doi.org/10.1002/ejoc.201100870openalex-snapshot
A Family of Thiazolium Salt Derived N‐Heterocyclic Carbenes (NHCs) for Organocatalysis: Synthesis, Investigation and Application in Cross‐Benzoin Condensation
inferred← citeshttps://doi.org/10.1002/ejoc.201100937openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Oxidative Esterification Reaction of Aldehydes with Alkyl Halides under Aerobic Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201300830openalex-snapshot
Enantiopure Chiral Concave N‐Heterocyclic Carbene Precursors
inferred← citeshttps://doi.org/10.1002/ejoc.201301366openalex-snapshot
Design, Synthesis, and Organocatalytic Activity of N‐Heterocyclic Carbenes Functionalized with Hydrogen‐Bond Donors in Enantioselective Reactions of Homoenolates
inferred← citeshttps://doi.org/10.1002/ejoc.201600228openalex-snapshot
Thiamine‐Diphosphate‐Dependent Enzymes as Catalytic Tools for the Asymmetric Benzoin‐Type Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201701625openalex-snapshot
Two‐Step One‐Pot Synthesis of Unsymmetrical (Hetero)Aryl 1,2‐Diketones by Addition‐Oxygenation of Potassium Aryltrifluoroborates to (Hetero)Arylacetonitriles
inferred← citeshttps://doi.org/10.1002/ejoc.202200548openalex-snapshot
Enantioselective Dual Catalysis of N‐Heterocyclic Carbene and Hydrogen‐Bond Donor Organocatalysts
inferred← citeshttps://doi.org/10.1002/ejoc.202400753openalex-snapshot
S‐Aryl Substitution Enhances Acidity of the 1,2,4‐Triazolium Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.202500389openalex-snapshot
Synthesis of a Library of Bifunctional N‐Heterocyclic Carbene Ligand Precursors with Hydrogen Bond Donor Subunits
inferred← citeshttps://doi.org/10.1002/hlca.201400076openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed α‐Alkylation of Ketones with Primary Alcohols
inferred← citeshttps://doi.org/10.1002/slct.202303139openalex-snapshot
Mechanistic Evaluation of Benzoin Catalysis Enabled by Triazolium Salt Application in the Preparation of Benzil and Heterocycles
inferred← citeshttps://doi.org/10.1002/slct.202503134openalex-snapshot
An Alternative Method for the Efficient Synthesis of Aminoindane‐Based Chiral Triazolium Salts
inferred← citeshttps://doi.org/10.1002/tcr.202300103openalex-snapshot
Remote Electronic Tuning of Chiral N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/tcr.70254openalex-snapshot
Mimicking Natural Catalytic Systems: Design Inspired Beyond the Traditional Paradigm
inferred← citeshttps://doi.org/10.1007/s10562-020-03417-3openalex-snapshot
N-PEGylated Thiazolium Salt: A Green and Reusable Homogenous Organocatalyst for the Synthesis of Benzoins and Acyloins
inferred← citeshttps://doi.org/10.1007/s10593-013-1230-4openalex-snapshot
Catalysis of Organic Reactions by Carbenes and Carbene Complexes
inferred← citeshttps://doi.org/10.1007/s11237-022-09710-zopenalex-snapshot
Modern Approaches to Synthetic Design of Chiral α-Tertiary Amines Based on Trifluoromethylcontaining Ketimines: A Review
inferred← citeshttps://doi.org/10.1007/s11426-012-4790-8openalex-snapshot
Ru-catalyzed highly enantioselective hydrogenation of α-keto Weinreb amides
inferred← citeshttps://doi.org/10.1007/s11426-023-1578-yopenalex-snapshot
Biomimetic asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00612-1openalex-snapshot
6.12 Benzoin and Stetter Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-096807-0.00008-7openalex-snapshot
Five-Membered Ring Systems: With More than One N Atom
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00118-xopenalex-snapshot
1.13 Benzoin and Aza-benzoin
inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00009-1openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-809270-5.00016-9openalex-snapshot
Application of Green Chemistry in Homogeneous Catalysis
inferred← citeshttps://doi.org/10.1016/b978-0-615-39515-9.50002-3openalex-snapshot
Formation of C-O Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-615-39515-9.50005-9openalex-snapshot
Formation of CC Bonds
inferred← citeshttps://doi.org/10.1016/bs.acat.2023.07.003openalex-snapshot
Boronic acids as additives in organic synthesis and catalysis
inferred← citeshttps://doi.org/10.1016/j.cej.2024.154280openalex-snapshot
Self-condensation for enhancing the hydrophilicity of covalent organic polymers and photocatalytic hydrogen generation with unprecedented apparent quantum yield up to 500 nm
inferred← citeshttps://doi.org/10.1016/j.jscs.2012.05.005openalex-snapshot
An investigation of the catalytic potential of potassium cyanide and imidazolium salts for ultrasound-assisted synthesis of benzoin derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2011.11.028openalex-snapshot
Asymmetric benzoin condensation promoted by chiral triazolium precatalyst bearing a pyridine moiety
inferred← citeshttps://doi.org/10.1016/j.tet.2012.09.095openalex-snapshot
An asymmetric intramolecular Stetter reaction catalyzed by a chiral triazolium precatalyst bearing a pyridine moiety
inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.066openalex-snapshot
Highly efficient synthesis of spirocyclic (1R)-camphor-derived triazolium salts: application in the catalytic asymmetric benzoin condensation
inferred← citeshttps://doi.org/10.1016/j.tet.2016.02.049openalex-snapshot
Enantioselective benzoin condensation catalyzed by spirocyclic terpene-based N-heterocyclic carbenes
inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.001openalex-snapshot
Asymmetric cross-benzoin condensation promoted by a chiral triazolium precatalyst bearing a pyridine moiety
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.06.002openalex-snapshot
Preparation of chiral 1,2,4-triazolium salts as new NHC precatalysts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.05.070openalex-snapshot
N-Heterocyclic carbene catalyzed intramolecular crossed aldehyde–ketone benzoin condensation in the chalcone of o-phthalaldehyde: a facile synthesis of naphthalenones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.019openalex-snapshot
Copper-catalyzed base-accelerated direct oxidation of C–H bond to synthesize benzils, isatins, and quinoxalines with molecular oxygen as terminal oxidant
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22008-7openalex-snapshot
Five Membered Ring Systems
inferred← citeshttps://doi.org/10.1021/acs.accounts.3c00171openalex-snapshot
New Strategies for the Functionalization of Carbonyl Derivatives via α-Umpolung: From Enolates to Enolonium Ions
inferred← citeshttps://doi.org/10.1021/acs.accounts.9b00635openalex-snapshot
Bifunctional N-Heterocyclic Carbenes Derived from l -Pyroglutamic Acid and Their Applications in Enantioselective Organocatalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00060openalex-snapshot
Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c03073openalex-snapshot
The Role of the Fused Ring in Bicyclic Triazolium Organocatalysts: Kinetic, X-ray, and DFT Insights
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00801openalex-snapshot
Accessing Diverse Cross-Benzoin and α-Siloxy Ketone Products via Acyl Substitution Chemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02747openalex-snapshot
Going Full Circle with Organocatalysis and Biocatalysis: The Latent Potential of Cofactor Mimics in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01632openalex-snapshot
Electrochemical Umpolung α-Alkoxylation of Thiophene-Containing Amides
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00301openalex-snapshot
Origin of Chemoselectivity in N-Heterocyclic Carbene Catalyzed Cross-Benzoin Reactions: DFT and Experimental Insights
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02829openalex-snapshot
Asymmetric Desymmetrization of 1,3-Diketones via Intramolecular Benzoin Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01755openalex-snapshot
An Acidity Scale of Triazolium-Based NHC Precursors in DMSO
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01821openalex-snapshot
Theoretical Study of Diastereoselective NHC-Catalyzed Cross-Benzoin Reactions between Furfural and N-Boc-Protected α-Amino Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03408openalex-snapshot
Chiral Benzoins via Asymmetric Transfer Hemihydrogenation of Benzils: The Detail that Matters
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02863openalex-snapshot
An Alternative Method for the Synthesis of N-Pentafluorophenyl Triazolium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00315openalex-snapshot
Bifunctional NHC-Catalyzed Asymmetric Intramolecular Conjugate Addition via Noncovalent Interaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03509openalex-snapshot
Chemoselective Umpolung of Enals for Asymmetric Homoenolate Cross-Annulation of Enals and Aldehydes Catalyzed by N-Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/acscatal.5b02410openalex-snapshot
Metal-Free Perfluoroarylation by Visible Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1021/acsomega.9b03109openalex-snapshot
Catalytic Preparation of 1-Aryl-Substituted 1,2,4-Triazolium Salts
inferred← citeshttps://doi.org/10.1021/am302163popenalex-snapshot
Facile Approach to Preparing Microporous Organic Polymers through Benzoin Condensation
inferred← citeshttps://doi.org/10.1021/ar2000716openalex-snapshot
Extending NHC-Catalysis: Coupling Aldehydes with Unconventional Reaction Partners
inferred← citeshttps://doi.org/10.1021/cs400602vopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Formal [3+2] Annulation of Alkynyl Aldehydes with Nitrosobenzenes: A Highly Regioselective Umpolung Strategy
inferred← citeshttps://doi.org/10.1021/ja308420copenalex-snapshot
Proton Transfer Reactions of Triazol-3-ylidenes: Kinetic Acidities and Carbon Acid p K a Values for Twenty Triazolium Salts in Aqueous Solution
inferred← citeshttps://doi.org/10.1021/ja501772mopenalex-snapshot
Chemoselective N-Heterocyclic Carbene-Catalyzed Cross-Benzoin Reactions: Importance of the Fused Ring in Triazolium Salts
inferred← citeshttps://doi.org/10.1021/ja508521aopenalex-snapshot
Dynamic Kinetic Asymmetric Cross-Benzoin Additions of β-Stereogenic α-Keto Esters
inferred← citeshttps://doi.org/10.1021/jacs.5b13104openalex-snapshot
Chiral Frustrated Lewis Pairs Catalyzed Highly Enantioselective Hydrosilylations of 1,2-Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1021/jacs.6b02929openalex-snapshot
Dynamic Kinetic Resolution Enabled by Intramolecular Benzoin Reaction: Synthetic Applications and Mechanistic Insights
inferred← citeshttps://doi.org/10.1021/jo101318uopenalex-snapshot
Enantioselective Synthesis of Indole-Fused Dihydropyranones via Catalytic Cycloaddition of Ketenes and 3-Alkylenyloxindoles
inferred← citeshttps://doi.org/10.1021/jo101791wopenalex-snapshot
Highly Chemoselective Direct Crossed Aliphatic−Aromatic Acyloin Condensations with Triazolium-Derived Carbene Catalysts
inferred← citeshttps://doi.org/10.1021/jo102582aopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Reaction of Phthalaldehydes: Controllable Stereoselective Synthesis of Polyhydroxylated Spiro- and Fused Indenones Dictated by the Structure of NHC Catalysts
inferred← citeshttps://doi.org/10.1021/jo500194dopenalex-snapshot
DFT Study on the Mechanisms and Stereoselectivities of the [4 + 2] Cycloadditions of Enals and Chalcones Catalyzed by N-Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/ol3018402openalex-snapshot
Biomass Conversion to High Value Chemicals: From Furfural to Chiral Hydrofuroins in Two Steps
inferred← citeshttps://doi.org/10.1021/ol400769topenalex-snapshot
Highly Chemo- and Enantioselective Cross-Benzoin Reaction of Aliphatic Aldehydes and α-Ketoesters
inferred← citeshttps://doi.org/10.1021/ol403762eopenalex-snapshot
Practical Approach for Preparation of Unsymmetric Benzils from β-Ketoaldehydes
inferred← citeshttps://doi.org/10.1021/ol501205vopenalex-snapshot
Bifunctional N-Heterocyclic Carbene-Catalyzed Highly Enantioselective Synthesis of Spirocyclic Oxindolo-β-lactams
inferred← citeshttps://doi.org/10.1021/ol502365ropenalex-snapshot
Chiral Spirooxindole–Butenolide Synthesis through Asymmetric N-Heterocyclic Carbene-Catalyzed Formal (3 + 2) Annulation of 3-Bromoenals and Isatins
inferred← citeshttps://doi.org/10.1021/ol5027415openalex-snapshot
N-Heterocyclic Carbene Organocatalytic Reductive β,β-Coupling Reactions of Nitroalkenes via Radical Intermediates
inferred← citeshttps://doi.org/10.1021/ol9026232openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Intramolecular Aldehyde−Nitrile Cross Coupling: An Easy Access to 3- Aminochromones
inferred← citeshttps://doi.org/10.1038/s41557-019-0258-1openalex-snapshot
Unravelling mechanistic features of organocatalysis with in situ modifications at the secondary sphere
inferred← citeshttps://doi.org/10.1038/srep12431openalex-snapshot
Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups
inferred← citeshttps://doi.org/10.1039/c0cc02013copenalex-snapshot
N-heterocyclic carbene catalysed asymmetric cross-benzoin reactions of heteroaromatic aldehydes with trifluoromethyl ketones
inferred← citeshttps://doi.org/10.1039/c0cc04839aopenalex-snapshot
Enantioselective [4+2] cycloaddition of ketenes and 1-azadienes catalyzed by N-heterocyclic carbenes
inferred← citeshttps://doi.org/10.1039/c0ob00249fopenalex-snapshot
Enantioselective formal [2+2] cycloaddition of ketenes with nitroso compounds catalyzed by N-heterocyclic carbenes
inferred← citeshttps://doi.org/10.1039/c1cc13860jopenalex-snapshot
Highly diastereo- and enantioselective NHC-catalyzed [3+2] annulation of enals and isatins
inferred← citeshttps://doi.org/10.1039/c1ob05854aopenalex-snapshot
N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives
inferred← citeshttps://doi.org/10.1039/c2cs15333eopenalex-snapshot
Organocatalytic umpolung: N-heterocyclic carbenes and beyond
inferred← citeshttps://doi.org/10.1039/c2sc00622gopenalex-snapshot
NHC-catalysed, chemoselective crossed-acyloin reactions
inferred← citeshttps://doi.org/10.1039/c2sc22137copenalex-snapshot
Mechanistic insights into the triazolylidene-catalysed Stetter and benzoin reactions: role of the N-aryl substituent
inferred← citeshttps://doi.org/10.1039/c3cc41588kopenalex-snapshot
The catalytic versatility of low toxicity dialkyltriazolium salts: in situ modification facilitates diametrically opposed catalysis modes in one pot
inferred← citeshttps://doi.org/10.1039/c3cc42597eopenalex-snapshot
Aerobic oxidation of NHC-catalysed aldehyde esterifications with alcohols: benzoin, not the Breslow intermediate, undergoes oxidation
inferred← citeshttps://doi.org/10.1039/c5dt04409jopenalex-snapshot
Catalytically active lead( ii )–imidazolium coordination assemblies with diversified lead( ii ) coordination geometries
inferred← citeshttps://doi.org/10.1039/c5sc00731copenalex-snapshot
Enantioselective annulation of enals with 2-naphthols by triazolium salts derived from l -phenylalanine
inferred← citeshttps://doi.org/10.1039/c7cc05561gopenalex-snapshot
Direct, efficient NHC-catalysed aldehyde oxidative amidation: in situ formed benzils as unconventional acylating agents
inferred← citeshttps://doi.org/10.1039/c7ob03005copenalex-snapshot
Highly chemoselective intermolecular cross-benzoin reactions using an ad hoc designed novel N-heterocyclic carbene catalyst
inferred← citeshttps://doi.org/10.1039/c8cc07407kopenalex-snapshot
Benzoins and cyclobenzoins in supramolecular and polymer chemistry
inferred← citeshttps://doi.org/10.1039/c8ob02192aopenalex-snapshot
An enantioselective assembly of naphthopyran via NHC-catalyzed [3 + 3] annulation of bromoenal with β-tetralone
inferred← citeshttps://doi.org/10.1039/c9cc05906gopenalex-snapshot
Intercepted dehomologation of aldoses by N-heterocyclic carbene catalysis – a novel transformation in carbohydrate chemistry
inferred← citeshttps://doi.org/10.1039/d0ob02017fopenalex-snapshot
Enantioselective N-heterocyclic carbene-catalysed intermolecular crossed benzoin condensations: improved catalyst design and the role of in situ racemisation
inferred← citeshttps://doi.org/10.1039/d1qo00743bopenalex-snapshot
Asymmetric synthesis of γ-lactams under low-loading N-heterocyclic carbene catalysis
inferred← citeshttps://doi.org/10.1055/a-1856-5688openalex-snapshot
Recent Advances in Enantioselective Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes (NHCs) Containing Triazolium Motifs
inferred← citeshttps://doi.org/10.1055/s-0037-1611733openalex-snapshot
Synthetic Approaches to Chiral Non-C 2-symmetric N-Heterocyclic Carbene Precursors
inferred← citeshttps://doi.org/10.1055/s-0040-1707326openalex-snapshot
Designing the Secondary Coordination Sphere in Small-Molecule Catalysis
inferred← citeshttps://doi.org/10.1055/sos-sd-224-00223openalex-snapshot
2.8 Recent Advances in N-Heterocyclic Carbene Organocatalysis
inferred← citeshttps://doi.org/10.1139/v11-157openalex-snapshot
Silicon and silicon oxide surface modification using thiamine-catalyzed benzoin condensations
inferred← citeshttps://doi.org/10.15826/chimtech.2023.10.2.14openalex-snapshot
Advancements in N-heterocyclic carbenes (NHCs) catalysis for benzoin reactions: A comprehensive review from past to present
inferred← citeshttps://doi.org/10.30564/opmr.v4i2.4953openalex-snapshot
N-heterocyclic Carbene Catalysed Polymerisation of 2,5-Diformylfuran
inferred← citeshttps://doi.org/10.33224/rrch.2024.69.7-8.05openalex-snapshot
Microwave-assisted N,N’-dimethylbenzimidazolium iodide as a powerful and efficient catalytic system for the intermolecular Stetter reaction and the synthesis of 1,2-diarylethane-1,2-dione derivatives in the absence of organic solvent
inferred← citeshttps://doi.org/10.3390/catal11091055openalex-snapshot
Triazolium Salt Organocatalysis: Mechanistic Evaluation of Unusual Ortho-Substituent Effects on Deprotonation
inferred← citeshttps://doi.org/10.3390/ma13163574openalex-snapshot
Organocatalytic Name Reactions Enabled by NHCs
inferred← citeshttps://doi.org/10.3762/bjoc.12.47openalex-snapshot
Recent advances in N-heterocyclic carbene (NHC)-catalysed benzoin reactions
inferred← citeshttps://doi.org/10.3762/bjoc.21.200openalex-snapshot
Visible-light-driven NHC and organophotoredox dual catalysis for the synthesis of carbonyl compounds
inferred← citeshttps://doi.org/10.3762/bjoc.8.169openalex-snapshot
N-Heterocyclic carbene-catalyzed direct cross-aza-benzoin reaction: Efficient synthesis of α-amino-β-keto esters
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.12.4408openalex-snapshot
Inverse Enantioselectivity with Catalyst Loading in Enantioselective Self-Benzoin Condensation using Triazolium-based N-Heterocyclic Carbene Catalyst
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.78.338openalex-snapshot
Development of Multi-functional NHC Catalysts bearing Pyridine Moiety: Application to Catalytic Asymmetric Reactions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.222openalex-snapshot
Remote Electronic Tuning for High-performance N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.5772/intechopen.100642openalex-snapshot
N-Heterocyclic Carbene Mediated Organocatalysis Reactions
inferred← citeshttps://doi.org/10.6023/cjoc202205031openalex-snapshot
α-Benzoyloxylation of β-Dicarbonyl Compounds Involving Cyclic Trivalent Iodine Reagents
inferred← citeshttps://doi.org/10.6023/cjoc202401009openalex-snapshot
N-Heterocyclic Carbene Catalyzed the Umpolung of Aldehyde Compounds
inferred← citeshttps://doi.org/10.70675/c3ba7b6dz9fb1z4280z9861zad23ec578f1aopenalex-snapshot
Catalytic asymmetric carbon-carbon bond formation with N-heterocyclic carbene-generated homoenolates
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.