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Activation of TMSCN by N-Heterocyclic Carbenes for Facile Cyanosilylation of Carbonyl Compounds
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://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
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/10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-uopenalex-snapshot
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
inferredcites →https://doi.org/10.1002/anie.200301714openalex-snapshot
N‐Heterocyclic Carbenes: Reagents, Not Just Ligands!
inferredcites →https://doi.org/10.1002/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferredcites →https://doi.org/10.1002/anie.200461572openalex-snapshot
Organocatalyzed Conjugate Umpolung of α,β‐Unsaturated Aldehydes for the Synthesis of γ‐Butyrolactones
inferredcites →https://doi.org/10.1002/hlca.19960790108openalex-snapshot
The Chemistry of Stable Carbenes. Part 2. Benzoin‐type condensations of formaldehyde catalyzed by stable carbenes
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/hlca.19960790712openalex-snapshot
The First Asymmetric Intramolecular Stetter Reaction. Preliminary Communication
inferredcites →https://doi.org/10.1016/j.jorganchem.2003.07.028openalex-snapshot
Phospha-palladacycles and N-heterocyclic carbene palladium complexes: efficient catalysts for CC-coupling reactions
inferredcites →https://doi.org/10.1016/j.tet.2004.08.081openalex-snapshot
Catalytic asymmetric synthesis of (S)-oxybutynin and a versatile intermediate for antimuscarinic agents
inferredcites →https://doi.org/10.1016/s0022-1139(03)00104-0openalex-snapshot
Preparation of TMS protected trifluoromethylated alcohols using trimethylamine N-oxide and trifluoromethyltrimethylsilane (TMSCF3)
inferredcites →https://doi.org/10.1016/s0040-4020(01)88595-1openalex-snapshot
Cyanotrimethylsilane as a versatile reagent for introducing cyanide functionality
inferredcites →https://doi.org/10.1016/s0040-4039(00)71375-xopenalex-snapshot
Synthesis of α-hydroxyamides via the cyanosilylation of aromatic ketones
inferredcites →https://doi.org/10.1021/cr020038popenalex-snapshot
Catalytic Enantioselective Strecker Reactions and Analogous Syntheses
inferredcites →https://doi.org/10.1021/cr980414zopenalex-snapshot
Catalytic Enantioselective Addition to Imines
inferredcites →https://doi.org/10.1021/ja00094a020openalex-snapshot
Photoelectron Spectroscopy of a Carbene/Silylene/Germylene Series
inferredcites →https://doi.org/10.1021/ja0173324openalex-snapshot
First Example of N-Heterocyclic Carbenes as Catalysts for Living Polymerization: Organocatalytic Ring-Opening Polymerization of Cyclic Esters
inferredcites →https://doi.org/10.1021/ja021084+openalex-snapshot
In Situ Generation of Carbenes: A General and Versatile Platform for Organocatalytic Living Polymerization
inferredcites →https://doi.org/10.1021/ja027411vopenalex-snapshot
A Highly Enantioselective Catalytic Intramolecular Stetter Reaction
inferredcites →https://doi.org/10.1021/ja038631ropenalex-snapshot
A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature
inferredcites →https://doi.org/10.1021/ja040021jopenalex-snapshot
Kinetic Resolution of Chiral α-Olefins Using Optically Active ansa-Zirconocene Polymerization Catalysts
inferredcites →https://doi.org/10.1021/ja044714bopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates: γ-Butyrolactones by Direct Annulations of Enals and Aldehydes
inferredcites →https://doi.org/10.1021/ja046991oopenalex-snapshot
Conversion of α-Haloaldehydes into Acylating Agents by an Internal Redox Reaction Catalyzed by Nucleophilic Carbenes
inferredcites →https://doi.org/10.1021/ja0520161openalex-snapshot
Catalytic Conjugate Additions of Carbonyl Anions under Neutral Aqueous Conditions
inferredcites →https://doi.org/10.1021/jo00088a068openalex-snapshot
Catalytic Aldol Reaction with Sm(HMDS)3 and Its Application for the Introduction of a Carbon-Carbon Triple Bond at C-13 in Prostaglandin Synthesis
inferredcites →https://doi.org/10.1021/jo00269a052openalex-snapshot
Alkylsilyl isoselenocyanate. A new silicon pseudohalide. Synthesis, characterization, and reaction with carbonyl compounds
inferredcites →https://doi.org/10.1021/jo0267551openalex-snapshot
Efficient Transesterification/Acylation Reactions Mediated byN-Heterocyclic Carbene Catalysts
inferredcites →https://doi.org/10.1021/jo035431popenalex-snapshot
Transesterification/Acylation of Secondary Alcohols Mediated by N -Heterocyclic Carbene Catalysts
inferredcites →https://doi.org/10.1021/ol0264760openalex-snapshot
N-Heterocyclic Carbenes as Versatile Nucleophilic Catalysts for Transesterification/Acylation Reactions
inferredcites →https://doi.org/10.1021/ol0267228openalex-snapshot
Expanding the Catalytic Activity of Nucleophilic N-Heterocyclic Carbenes for Transesterification Reactions
inferredcites →https://doi.org/10.1021/ol048211mopenalex-snapshot
N-Heterocyclic Carbenes as Highly Efficient Catalysts for the Cyclotrimerization of Isocyanates
inferredcites →https://doi.org/10.1021/ol050100fopenalex-snapshot
Conversion of α,β-Unsaturated Aldehydes into Saturated Esters: An Umpolung Reaction Catalyzed by Nucleophilic Carbenes
inferredcites →https://doi.org/10.1021/ol050174ropenalex-snapshot
Enantioselective Acylation of Secondary Alcohols Catalyzed by Chiral N-Heterocyclic Carbenes
inferredcites →https://doi.org/10.1021/ol050568iopenalex-snapshot
N-Heterocyclic Carbene Catalyzed Trifluoromethylation of Carbonyl Compounds
inferredcites →https://doi.org/10.1021/ol050773yopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Amidation of Unactivated Esters with Amino Alcohols
inferredcites →https://doi.org/10.1039/b302062bopenalex-snapshot
Nucleophilic acylation of arylfluorides catalyzed by imidazolidenyl carbene
inferredcites →https://doi.org/10.1248/cpb.46.390openalex-snapshot
Catalytic Action of Azolium Salts. IX. Synthesis of 6-Aroyl-9H-purines and Their Analogues by Nucleophilic Aroylation Catalyzed by Imidazolium or Benzimidazolium Salt.
inferredcites →https://doi.org/10.3987/com-98-s54openalex-snapshot
Synthesis of 2-Aroylquinoxalines, 1-Aroylphthalazines, and 4-Aroylcinnolines; an Aroylation Method Using Arenecarbaldehydes Catalyzed by Azolium Salt
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.4647549openalex-extracted
B(C6f5)3-Catalyzed Regio- and Stereoselective Cyanation of Isatogens and Their Derivatives
inferred← citeshttps://doi.org/10.1002/047084289x.rn00916openalex-snapshot
1,3-Di-tert-butylimidazol-2-ylidene
inferred← citeshttps://doi.org/10.1002/9780470669587.ch1openalex-snapshot
Reactions of Aldehydes and Ketones and their Derivatives
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11447openalex-snapshot
Trimethylsilyl cyanide
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Trimethylsilyl Cyanide
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Trimethylsilyl cyanide
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Trimethylsilyl cyanide
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N‐Heterocyclic Carbene‐Catalyzed C–C Bond Formation
inferred← citeshttps://doi.org/10.1002/9781118662083.cot07-009openalex-snapshot
Formation of Alcohols and Phenols by Alkylation of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/9783527675142.ch27openalex-snapshot
Catalysis with Stable Carbenes ( n ?→?π*)
inferred← citeshttps://doi.org/10.1002/9783527675142.ch8openalex-snapshot
Mechanism of C – Si Bond Cleavage Using Lewis Bases ( n → σ*)
inferred← citeshttps://doi.org/10.1002/adsc.200800673openalex-snapshot
Highly Efficient Cyanosilylation of Sterically Bulky Ketones Catalyzed by Tin Ion‐Exchanged Montmorillonite
inferred← citeshttps://doi.org/10.1002/adsc.200800815openalex-snapshot
Hydrosilylation of Ketone and Imine over Poly‐N‐Heterocyclic Carbene Particles
inferred← citeshttps://doi.org/10.1002/adsc.200900538openalex-snapshot
N‐Heterocyclic Carbene‐Mediated Enantioselective Addition of Phenols to Unsymmetrical Alkylarylketenes
inferred← citeshttps://doi.org/10.1002/adsc.200900658openalex-snapshot
Polymer‐Supported, Carbon Dioxide‐Protected N‐Heterocyclic Carbenes: Synthesis and Application in Organo‐ and Organometallic Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.200900816openalex-snapshot
N‐Heterocyclic Carbene‐Mediated Organocatalytic Transfer of Tin onto Aldehydes: New Access to α‐Silyloxyalkylstannanes and γ‐Silyloxyallylstannanes
inferred← citeshttps://doi.org/10.1002/adsc.201200063openalex-snapshot
N‐Heterocyclic Carbene‐Mediated Organocatalytic Transfer of Tin onto Aldehydes: An Easy Access to syn‐Diols and Mechanistic Studies
inferred← citeshttps://doi.org/10.1002/ajoc.201500348openalex-snapshot
N‐Heterocyclic‐Carbene‐Catalysed Diastereoselective Vinylogous Mukaiyama/Michael Reaction of 2‐(Trimethylsilyloxy)furan and Enones
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Well‐Defined Binuclear Co(II) Complexes: Synthesis, Structure, Characterizations and Catalytic Applications in Cyanosilylation of Various Aldehydes under Solvent‐Free Conditions
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.200702288openalex-snapshot
Encapsulated N‐Heterocyclic Carbenes in Silicones without Reactivity Modification
inferred← citeshttps://doi.org/10.1002/ange.200800490openalex-snapshot
Harnessing the Potential of N‐Heterocyclic Carbenes for the Rejuvenation of Group‐Transfer Polymerization of (Meth)Acrylics
inferred← citeshttps://doi.org/10.1002/ange.200806058openalex-snapshot
Conversion of Carbon Dioxide into Methanol with Silanes over N‐Heterocyclic Carbene Catalysts
inferred← citeshttps://doi.org/10.1002/anie.200603380openalex-snapshot
N‐Heterocyclic Carbenes as Organocatalysts
inferred← citeshttps://doi.org/10.1002/anie.200604943openalex-snapshot
Lewis Base Catalysis in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200702288openalex-snapshot
Encapsulated N‐Heterocyclic Carbenes in Silicones without Reactivity Modification
inferred← citeshttps://doi.org/10.1002/anie.200800490openalex-snapshot
Harnessing the Potential of N‐Heterocyclic Carbenes for the Rejuvenation of Group‐Transfer Polymerization of (Meth)Acrylics
inferred← citeshttps://doi.org/10.1002/anie.200806058openalex-snapshot
Conversion of Carbon Dioxide into Methanol with Silanes over N‐Heterocyclic Carbene Catalysts
inferred← citeshttps://doi.org/10.1002/aoc.1189openalex-snapshot
Aluminum phthalocyanine: an active and simple catalyst for cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1002/aoc.1204openalex-snapshot
Solvent‐free cyanosilylation of ketones with (CH3)3SiCN (TMSCN) catalyzed by NbF5
inferred← citeshttps://doi.org/10.1002/aoc.1324openalex-snapshot
Solvent‐free cyanosilylation of aldehydes catalyzed by SmI2
inferred← citeshttps://doi.org/10.1002/aoc.1416openalex-snapshot
Copper perchlorate hexahydrate: a highly efficient catalyst for the cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1002/aoc.1600openalex-snapshot
Organocatalytic synthesis of cyanohydrin trimethylsilyl ethers by potassium 4‐benzylpiperidinedithiocarbamate under solvent‐free conditions
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Comparison of Superparamagnetic Fe 3 O 4 ‐Supported N‐Heterocyclic Carbene‐Based Catalysts for Enantioselective Allylation
inferred← citeshttps://doi.org/10.1002/cctc.201200721openalex-snapshot
Mechanistic Insights into the Reduction of Carbon Dioxide with Silanes over N‐Heterocyclic Carbene Catalysts
inferred← citeshttps://doi.org/10.1002/chem.200701013openalex-snapshot
Synthesis and Characterization of [Cu(NHC) 2 ]X Complexes: Catalytic and Mechanistic Studies of Hydrosilylation Reactions
inferred← citeshttps://doi.org/10.1002/chem.201001120openalex-snapshot
N‐Heterocyclic Carbene Mediated Activation of Tetravalent Silicon Compounds: A Critical Evaluation
inferred← citeshttps://doi.org/10.1002/chem.201101195openalex-snapshot
Mild and Efficient Trimethylsilylcyanation of Ketones Catalysed by PNP Chloride
inferred← citeshttps://doi.org/10.1002/chem.201204539openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [4+2] Cycloaddition of Nitroalkenes with Oxodienes
inferred← citeshttps://doi.org/10.1002/chem.201404204openalex-snapshot
Germylene Cyanide Complex: A Reagent for the Activation of Aldehydes with Catalytic Significance
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inferred← citeshttps://doi.org/10.1002/chin.200625094openalex-snapshot
Activation of TMSCN by N‐Heterocyclic Carbenes for Facile Cyanosilylation of Carbonyl Compounds.
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N‐Heterocyclic Carbene‐Catalysed Direct Synthesis of Cyano Esters via Cyanation‐Esterification Reaction of α‐Keto Esters
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Recent Advances in Carbon Dioxide Capture, Fixation, and Activation by using N‐Heterocyclic Carbenes
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N‐Heterocyclic Carbene: An Efficient Catalyst for the Ring‐Opening Reaction of Aziridine with Acid Anhydride
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inferred← citeshttps://doi.org/10.1002/ejoc.200800297openalex-snapshot
Uncatalyzed Strecker‐Type Reaction of N,N‐Dialkylhydrazones in Pure Water
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Stereoselective Synthesis of (2E,4Z)‐Dienamides Employing (Triphenylphosphoranylidene)ketene
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Asymmetric Cyanosilylation of α‐Keto Esters Catalyzed by the [Ru(phgly)2(binap)]–C6H5OLi System
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inferred← citeshttps://doi.org/10.1002/slct.201700946openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/2789_2008_079openalex-snapshot
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Insertion of CO2 into E–X Bonds
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inferred← citeshttps://doi.org/10.1007/s13738-014-0582-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00124-5openalex-snapshot
1.18 CN Addition to CO and CN Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00094-1openalex-snapshot
Nitriles: General Methods and Aliphatic Nitriles
inferred← citeshttps://doi.org/10.1016/j.apcata.2010.06.019openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.apcata.2014.09.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.catcom.2007.11.030openalex-snapshot
N-Iodosuccinimide (NIS) a novel and effective catalyst for the cyanosilylation of aldehydes under mild reaction conditions
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.11.032openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.catcom.2008.10.036openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cclet.2011.06.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cclet.2013.11.034openalex-snapshot
N-Heterocyclic carbene-catalyzed synthesis of acetyltributylcitrate via a transesterification reaction
inferred← citeshttps://doi.org/10.1016/j.ica.2007.11.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ica.2017.07.004openalex-snapshot
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Solvent-free cyanosilylation of aromatic and heteroaryl aldehydes catalyzed by a cationic iron N-heterocyclic carbene complex at ambient temperature under UV irradiation
inferred← citeshttps://doi.org/10.1016/j.ica.2020.120006openalex-snapshot
Cyanosilylation of carbonyl compounds catalyzed by half-sandwich (η6-p-cymene) Ruthenium(II) complexes bearing heterocyclic hydrazone derivatives
inferred← citeshttps://doi.org/10.1016/j.ica.2023.121801openalex-snapshot
Biphenol-based tetradentate N2O2 donor scaffold binuclear Zn(II) and trinuclear Cu(II) Complexes: Synthesis, Structure, Characterizations, and catalytic cyanosilylation of aldehydes at room temperature
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2011.09.012openalex-snapshot
NHC-catalyzed generation of difluorocarbene and its application to difluoromethylation of oxygen nucleophiles
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2006.10.006openalex-snapshot
Catalytic activity of N-heterocyclic carbenes in ring opening polymerization of cyclic siloxanes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.05.005openalex-snapshot
New N-heterocyclic carbene silver(I) and mercury(II) 2-D supramolecular layers by the π–π stacking interactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.07.011openalex-snapshot
Fe(Cp)2PF6: An efficient catalyst for cyanosilylation of carbonyl compounds under solvent free condition
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2007.09.027openalex-snapshot
New mercury(II) and silver(I) complexes containing NHC metallacrown ethers with the π–π stacking interactions
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.01.058openalex-snapshot
Activation of trimethylsilyl cyanide by potassium phthalimide for facile synthesis of TMS-protected cyanohydrins
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.08.009openalex-snapshot
Highly efficient chemo- and regioselective silylation of –OH groups and cyanosilylation of aldehydes promoted by TiCl2(OTf)–SiO2 as a new recyclable catalyst
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.07.030openalex-snapshot
Cyanosilylation of aldehydes catalyzed by arylhydrazone di- and triorganotin(IV) complexes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.08.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121171openalex-snapshot
Multinuclear Zn(II)-arylhydrazone complexes as catalysts for cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.jscs.2014.03.003openalex-snapshot
N-heterocyclic carbene catalyzed synthesis of dimethyl carbonate via transesterification of ethylene carbonate with methanol
inferred← citeshttps://doi.org/10.1016/j.molcata.2007.12.007openalex-snapshot
Potassium phthalimide-N-oxyl: An efficient catalyst for cyanosilylation of carbonyl compounds under mild conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2016.11.036openalex-snapshot
Effective cyanosilylation of aldehydes with copper(II)-based polymeric catalysts
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.08.051openalex-snapshot
Synthesis, structural characterization and properties of new N-heterocyclic carbene Ag(I) complexes
inferred← citeshttps://doi.org/10.1016/j.poly.2007.08.046openalex-snapshot
New N-heterocyclic carbene mercury(II) and silver(I) complexes
inferred← citeshttps://doi.org/10.1016/j.poly.2018.07.036openalex-snapshot
Acidic and basic sites of M2DEBDC (M = Mg or Mn and E = O or S) acting as catalysts for cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.009openalex-snapshot
Kinetics and mechanism of base catalysed ethyl cyanoformate addition to aldehydes
inferred← citeshttps://doi.org/10.1016/j.tet.2015.11.044openalex-snapshot
N-heterocyclic carbene-catalysed Peterson olefination reaction
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.03.020openalex-snapshot
Experimental and theoretical studies on the asymmetric cyanosilylation of C2-symmetric hydrazones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.03.001openalex-snapshot
Chiral relay in NHC-mediated asymmetric β-lactam synthesis I; substituent effects in NHCs derived from (1R,2R)-cyclohexane-1,2-diamine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.05.030openalex-snapshot
Bis-TADDOLs as bifunctional organocatalysts for trifluoromethylation of aldehydes and ring-opening of cyclohexene oxide with p-toluidine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.04.106openalex-snapshot
Iron(III) triflate-catalyzed one-pot synthesis of acetal-type protected cyanohydrins from carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.10.157openalex-snapshot
Synthesis of optically active imidazopyridinium salts and the corresponding NHCs
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.132openalex-snapshot
Catalytic cyanosilylation of ketones with simple phosphonium salt
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.090openalex-snapshot
An expeditious synthesis of cyanohydrin trimethylsilyl ethers using tetraethylammonium 2-(carbamoyl)benzoate as a bifunctional organocatalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.06.138openalex-snapshot
A tricyclic aluminum alkoxide catalyst for aldehyde trimethylsilylcyanation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.02.063openalex-snapshot
α,β-Unsaturated acyl cyanide synthesis via triethylamine catalyzed redox cyanation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.10.119openalex-snapshot
N-heterocyclic carbene catalyzed cyanation reaction of carbonyl compounds with ethyl cyanoformate and acetyl cyanide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.070openalex-snapshot
Polystyrene-supported TBD as an efficient and reusable organocatalyst for cyanosilylation of aldehydes, ketones, and imines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.02.026openalex-snapshot
Rapid additions of bulky tert-butyldimethylsilyl cyanide to hindered ketones promoted by heterogeneous tin ion-exchanged montmorillonite catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.02.080openalex-snapshot
N-Heterocyclic carbene-catalyzed cyanomethylation of aldehydes with TMSAN
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.034openalex-snapshot
Asymmetric induction by helical poly(amino acid)s in cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.034openalex-snapshot
N-heterocyclic carbene-mediated transformations of silicon reagents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.006openalex-snapshot
Synthesis of magnetically recoverable imidazolium hydrogen carbonate and its application as an N-heterocyclic carbene catalyst to cyanosilylation of aldehydes and ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154909openalex-snapshot
B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
inferred← citeshttps://doi.org/10.1016/j.theochem.2008.05.016openalex-snapshot
Computational study on 1,1,3,3-tetramethylguanidine-catalyzed cyanosilylation mechanism of hypnone
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c00819openalex-snapshot
Half-Sandwich Ruthenium Complexes with Hydrazone Ligands: Preparation, Structure, and Catalytic Activity in Cyanosilylether Synthesis under an Air Atmosphere
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01242openalex-snapshot
Application of an Electrochemical Microflow Reactor for Cyanosilylation: Machine Learning-Assisted Exploration of Suitable Reaction Conditions for Semi-Large-Scale Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00716openalex-snapshot
Targeted and Systematic Approach to the Study of pKa Values of Imidazolium Salts in Dimethyl Sulfoxide
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03347openalex-snapshot
Carbonyl-Stabilized Phosphorus Ylide as an Organocatalyst for Cyanosilylation Reactions Using TMSCN
inferred← citeshttps://doi.org/10.1021/acs.jpca.5b08676openalex-snapshot
Theoretical Insights on the Interaction of N-Heterocyclic Carbenes with Tetravalent Silicon Reagents
inferred← citeshttps://doi.org/10.1021/acs.organomet.2c00242openalex-snapshot
Theoretical Insights into Aluminum-Catalyzed Cyanosilylation of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03677openalex-snapshot
Fluoride-Mediated Nucleophilic Aromatic Amination of Chloro-1H-1,2,3-triazolium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00508openalex-snapshot
N-Heterocyclic Carbene Catalyzed 1,6-Conjugate Addition of Me3Si-CN to para-Quinone Methides and Fuchsones: Access to α-Arylated Nitriles
inferred← citeshttps://doi.org/10.1021/acsomega.0c06270openalex-snapshot
Cu(II)-Containing Metal–Organic Framework with 1D Hexagonal Channels for Cyanosilylation Reaction and Anticancer Activity on Osteosarcoma Cells
inferred← citeshttps://doi.org/10.1021/acsomega.7b02090openalex-snapshot
Cyanosilylation of Aromatic Aldehydes by Cationic Ruthenium(II) Complexes of Benzimidazole-Derived O-Functionalized N-Heterocyclic Carbenes at Ambient Temperature under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1021/cr068372zopenalex-snapshot
Organocatalysis by N-Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1021/cr800421copenalex-snapshot
Recent Progress in Lewis Base Activation and Control of Stereoselectivity in the Additions of Trimethylsilyl Nucleophiles
inferred← citeshttps://doi.org/10.1021/ja103531zopenalex-snapshot
The Catalytic Role of N-Heterocyclic Carbene in a Metal-Free Conversion of Carbon Dioxide into Methanol: A Computational Mechanism Study
inferred← citeshttps://doi.org/10.1021/ja809246fopenalex-snapshot
N-Heterocyclic Carbene-Induced Zwitterionic Ring-Opening Polymerization of Ethylene Oxide and Direct Synthesis of α,ω-Difunctionalized Poly(ethylene oxide)s and Poly(ethylene oxide)- b -poly(ε-caprolactone) Block Copolymers
inferred← citeshttps://doi.org/10.1021/jo301597hopenalex-snapshot
Imidazolium Hydrogen Carbonates versus Imidazolium Carboxylates as Organic Precatalysts for N-Heterocyclic Carbene Catalyzed Reactions
inferred← citeshttps://doi.org/10.1021/jo502155jopenalex-snapshot
On the Reaction of Diaminocarbenes with Aroylimines
inferred← citeshttps://doi.org/10.1021/jo702720aopenalex-snapshot
Probing the Efficiency of N-Heterocyclic Carbene Promoted O- to C-Carboxyl Transfer of Oxazolyl Carbonates
inferred← citeshttps://doi.org/10.1021/ma900679popenalex-snapshot
Group Transfer Polymerization of (Meth)acrylic Monomers Catalyzed by N-Heterocyclic Carbenes and Synthesis of All Acrylic Block Copolymers: Evidence for an Associative Mechanism
inferred← citeshttps://doi.org/10.1021/ma902676ropenalex-snapshot
N-Heterocyclic Carbene-Organocatalyzed Ring-Opening Polymerization of Ethylene Oxide in the Presence of Alcohols or Trimethylsilyl Nucleophiles as Chain Moderators for the Synthesis of α,ω-Heterodifunctionalized Poly(ethylene oxide)s
inferred← citeshttps://doi.org/10.1021/ol0630494openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Mukaiyama Aldol Reactions
inferred← citeshttps://doi.org/10.1021/ol0710515openalex-snapshot
N-Heterocyclic Carbene-Initiated α-Acylvinyl Anion Reactivity: Additions of α-Hydroxypropargylsilanes to Aldehydes
inferred← citeshttps://doi.org/10.1021/ol703025bopenalex-snapshot
N-Heterocyclic Carbene-Catalyzed Silyl Enol Ether Formation
inferred← citeshttps://doi.org/10.1021/om400791ropenalex-snapshot
Carbene-Bound Borane and Silane Adducts: A Comprehensive DFT Study on Their Stability and Propensity for Hydride-Mediated Ring Expansion
inferred← citeshttps://doi.org/10.1021/om500924qopenalex-snapshot
Synthesis, Characterization, and Reactivity of Lanthanide Amides Incorporating Neutral Pyrrole Ligand. Isolation and Characterization of Active Catalyst for Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.1038/srep42699openalex-snapshot
1-Ethyl-3-methylimidazolium acetate as a highly efficient organocatalyst for cyanosilylation of carbonyl compounds with trimethylsilyl cyanide
inferred← citeshttps://doi.org/10.1039/9781849732161-00399openalex-snapshot
N-Heterocyclic Carbenes as Organic Catalysts
inferred← citeshttps://doi.org/10.1039/b515102nopenalex-snapshot
N-Heterocyclic carbenes: Advances in transition metal and organic catalysis
inferred← citeshttps://doi.org/10.1039/b614412hopenalex-snapshot
N-Heterocyclic carbenes: advances in transition metal-mediated transformations and organocatalysis
inferred← citeshttps://doi.org/10.1039/b718462jopenalex-snapshot
Remarkable acceleration of cyanosilylation by the mesoporous Al-MCM-41 catalyst
inferred← citeshttps://doi.org/10.1039/b815139copenalex-snapshot
Asymmetric esterification of ketenes catalyzed by an N-heterocyclic carbene
inferred← citeshttps://doi.org/10.1039/c1ob05695fopenalex-snapshot
Unsymmetric salen ligands bearing a Lewis base: intramolecularly cooperative catalysis for cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1039/c2cy20037fopenalex-snapshot
Tetraethylammonium 2-(N-hydroxycarbamoyl)benzoate: a powerful bifunctional metal-free catalyst for efficient and rapid cyanosilylation of carbonyl compounds under mild conditions
inferred← citeshttps://doi.org/10.1039/c2gc36442eopenalex-snapshot
Efficient synthesis of cyanohydrin trimethylsilyl ethers via 1,2-chemoselective cyanosilylation of carbonyls
inferred← citeshttps://doi.org/10.1039/c2ob25188dopenalex-snapshot
Kinetics and mechanism of the racemic addition of trimethylsilyl cyanide to aldehydes catalysed by Lewis bases
inferred← citeshttps://doi.org/10.1039/c3dt32983fopenalex-snapshot
N-Heterocyclic carbene-initiated hydrosilylation of styryl alcohols with dihydrosilanes: a mechanistic investigation
inferred← citeshttps://doi.org/10.1039/c4ra08727eopenalex-snapshot
NHC catalysed trimethylsilylation of terminal alkynes and indoles with Ruppert's reagent under solvent free conditions
inferred← citeshttps://doi.org/10.1039/c5ra05487gopenalex-snapshot
N-heterocyclic carbene-catalysed pentafluorophenylation of aldehydes
inferred← citeshttps://doi.org/10.1039/c6ra14894hopenalex-snapshot
Syntheses, structures and catalytic properties of organic–inorganic hybrid materials constructed from Evans–Showell-type polyoxometalates and zinc–organic coordination units
inferred← citeshttps://doi.org/10.1039/c7cc03948dopenalex-snapshot
Metal free mild and selective aldehyde cyanosilylation by a neutral penta-coordinate silicon compound
inferred← citeshttps://doi.org/10.1039/c8gc03391aopenalex-snapshot
Design of high-performance heterogeneous catalysts using hydrotalcite for selective organic transformations
inferred← citeshttps://doi.org/10.1039/c9cc08975fopenalex-snapshot
The direct trifluoromethylsilylation and cyanosilylation of aldehydes via an electrochemically induced intramolecular pathway
inferred← citeshttps://doi.org/10.1039/d1ob00065aopenalex-snapshot
An N-heterocyclic carbene-catalyzed switchable reaction of 9-(trimethylsilyl)fluorene and aldehydes: chemoselective synthesis of dibenzofulvenes and fluorenyl alcohols
inferred← citeshttps://doi.org/10.1039/d3dt01617jopenalex-snapshot
Half-sandwich iridium complexes with hydrazone ligands: preparation, structure, and catalytic synthesis of cyanosilylethers under air
inferred← citeshttps://doi.org/10.1039/d5nj01256bopenalex-snapshot
Uncovering a solvent-free eco-friendly cyanosilylation of aldehydes through a well-defined gold( i )-NHC heterogeneous catalyst
inferred← citeshttps://doi.org/10.1039/d5qi01569copenalex-snapshot
Mesoionic imines: strong N-donors, electronic ambivalence and applications in catalysis
inferred← citeshttps://doi.org/10.1055/sos-sd-119-00082openalex-snapshot
19.5.14.15 Synthesis from Nitriles with Retention of the Cyano Group (Update 2013)
inferred← citeshttps://doi.org/10.1071/ch16566openalex-snapshot
N-Heterocyclic Carbene-Catalysed Mukaiyama–Michael Reaction and Mukaiyama Aldol/Mukaiyama–Michael Three-Component Coupling Reaction*
inferred← citeshttps://doi.org/10.1071/ch17595openalex-snapshot
Cyanosilylation of Aldehydes Catalyzed by Iron(iii) Arylhydrazone-ß-Diketone Complexes
inferred← citeshttps://doi.org/10.1073/pnas.0611309104openalex-snapshot
Effect of carbonates/phosphates as nucleophilic catalysts in dimethylformamide for efficient cyanosilylation of aldehydes and ketones
inferred← citeshttps://doi.org/10.1080/00304940809458105openalex-snapshot
IMPROVED THREE-COMPONENT LEWIS ACID-FREE APPROACH FOR THE SYNTHESIS OF PROTECTED RACEMIC CYANOHYDRINS
inferred← citeshttps://doi.org/10.1080/00397910701226897openalex-snapshot
Novel Uncatalyzed Hydrocyanation of Ketones utlizing Tetrachlorosilane–Potassium Cyanide Reagent
inferred← citeshttps://doi.org/10.1080/00397910802238791openalex-snapshot
Cyanosilylation of Aldehydes and Ketones Catalyzed by Nanocrystalline Magnesium Oxide
inferred← citeshttps://doi.org/10.1080/00397911.2016.1241884openalex-snapshot
TBD-catalyzed cyanosilylation of aldehydes and ketones
inferred← citeshttps://doi.org/10.1080/17458080.2020.1729356openalex-snapshot
A new heterometallic MOF with 1D nano-sized channels for cyanosilylation reaction and prevention effect against arrhythmia by reducing the sympathetic excitability
inferred← citeshttps://doi.org/10.1139/v2012-013openalex-snapshot
Citric acid as a trifunctional organocatalyst for thiocyanation of aromatic and heteroaromatic compounds in aqueous media
inferred← citeshttps://doi.org/10.1246/bcsj.20190260openalex-snapshot
[Retracted] A New Heterometallic MOF in Cyanosilylation Reaction, Treatment and Care Management Value in Stroke by Reducing Oxidative Stress Damage
inferred← citeshttps://doi.org/10.1246/cl.2011.1189openalex-snapshot
N -Heterocyclic Carbene-catalyzed Difluorocarbene Generation and its Application to Aryl Difluoromethyl Ether Synthesis
inferred← citeshttps://doi.org/10.1248/cpb.54.1653openalex-snapshot
Synthesis of Heterocyclic Compounds via Nucleophilic Aroylation Catalyzed by Imidazolidenyl Carbene
inferred← citeshttps://doi.org/10.1248/cpb.56.57openalex-snapshot
N-Heterocyclic Carbene Ligands in Copper-Catalyzed Addition of Diethylzinc to N-Sulfonylimines
inferred← citeshttps://doi.org/10.1248/yakushi.128.1179openalex-snapshot
Development of C-C Bond Formation and Asymmetric Reactions Catalyzed by N-Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.2174/1570179415666181114111939openalex-snapshot
The Hydrosilylation and Cyanosilylation of Ketones Catalyzed using Metal Borohydrides
inferred← citeshttps://doi.org/10.3390/catal6090128openalex-snapshot
Organocatalysis: Fundamentals and Comparisons to Metal and Enzyme Catalysis
inferred← citeshttps://doi.org/10.3390/catal7090260openalex-snapshot
Polyoxometalate (POM)-Layered Double Hydroxides (LDH) Composite Materials: Design and Catalytic Applications
inferred← citeshttps://doi.org/10.3390/catal9030284openalex-snapshot
Cyanosilylation of Aldehydes Catalyzed by Ag(I)- and Cu(II)-Arylhydrazone Coordination Polymers in Conventional and in Ionic Liquid Media
inferred← citeshttps://doi.org/10.3390/molecules31071108openalex-snapshot
The Progress in NHC-Catalyzed Synthesis of Organosilicon Derivatives
inferred← citeshttps://doi.org/10.5012/bkcs.2006.27.11.1907openalex-snapshot
Aluminium Phthalocyanine: An Active and Simple Catalyst for Cyanosilylation of Ketones
inferred← citeshttps://doi.org/10.5012/bkcs.2008.29.7.1320openalex-snapshot
Phosphomolybdic Acid Supported on Silica Gel as an Efficient and Reusable Catalyst for Cyanosilylation of Aldehydes
inferred← citeshttps://doi.org/10.6023/cjoc202303002openalex-snapshot
Recent Advances in the Synthesis of Cyanides Enabled by N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.6023/cjoc202306014openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Synthesis of Pentafluorophenyl Sulfides
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