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Advances in C–CN Bond Formation via C–H Bond Activation
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Transition Metal Catalyzed Coupling Reactions under C−H Activation
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Preparation and synthetic applications of cyano compounds
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Comprehensive Organic Transformations
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Iron‐Catalyzed Oxidative Mono‐ and Bis‐Phosphonation of N,N‐Dialkylanilines
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Copper‐Catalyzed Decarboxylative CN Triple Bond Formation: Direct Synthesis of Benzonitriles from Phenylacetic Acids Under O2 Atmosphere
inferredcites →https://doi.org/10.1002/adsc.201401152openalex-snapshot
Rhodium(III)‐Catalyzed Selective CH Cyanation of Indolines and Indoles with an Easily Accessible Cyano Source
inferredcites →https://doi.org/10.1002/anie.200805601openalex-snapshot
Asymmetric Intramolecular Carbocyanation of Alkenes by CC Bond Activation
inferredcites →https://doi.org/10.1002/anie.200903838openalex-snapshot
Direct Transformation of Methyl Arenes to Aryl Nitriles at Room Temperature
inferredcites →https://doi.org/10.1002/anie.201000723openalex-snapshot
Isocyanides in the Synthesis of Nitrogen Heterocycles
inferredcites →https://doi.org/10.1002/anie.201006044openalex-snapshot
A General Rhodium‐Catalyzed Cyanation of Aryl and Alkenyl Boronic Acids
inferredcites →https://doi.org/10.1002/anie.201106628openalex-snapshot
A Fascinating Journey into History: Exploration of the World of Isonitriles En Route to Complex Amides
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Synthesis of Aromatic Nitriles Using Nonmetallic Cyano‐Group Sources
inferredcites →https://doi.org/10.1002/anie.201307778openalex-snapshot
Continuous‐Flow Oxidative Cyanation of Primary and Secondary Amines Using Singlet Oxygen
inferredcites →https://doi.org/10.1002/anie.201309791openalex-snapshot
Iron(II)‐Catalyzed Direct Cyanation of Arenes with Aryl(cyano)iodonium Triflates
inferredcites →https://doi.org/10.1002/anie.201402449openalex-snapshot
Copper‐Catalyzed Regioselective ortho CH Cyanation of Vinylarenes
inferredcites →https://doi.org/10.1002/anie.201409247openalex-snapshot
Cobalt‐Catalyzed CH Cyanation of Arenes and Heteroarenes
inferredcites →https://doi.org/10.1002/anie.201508294openalex-snapshot
Regio‐ and Stereospecific 1,3‐Allyl Group Transfer Triggered by a Copper‐Catalyzed Borylation/ ortho ‐Cyanation Cascade
inferredcites →https://doi.org/10.1002/cber.18840170219openalex-snapshot
Ueber die Ersetzung der Amidgruppe durch Chlor in den aromatischen Substanzen
inferredcites →https://doi.org/10.1002/cber.19190520840openalex-snapshot
Das am Ringkohlenstoff gebundene Halogen und sein Ersatz durch andere Substituenten. I. Mitteilung: Ersatz des Halogens durch die Carboxylgruppe
inferredcites →https://doi.org/10.1002/cctc.201301076openalex-snapshot
Rhodium Catalyzed ortho‐Cyanation of Arylphosphates with N‐cyano‐N‐phenyl‐p‐toluenesulfonamide
inferredcites →https://doi.org/10.1002/chem.201000086openalex-snapshot
A Convenient Synthesis of Benzonitriles via Electrophilic Cyanation with N‐Cyanobenzimidazole
inferredcites →https://doi.org/10.1002/chem.201001363openalex-snapshot
Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium Catalysis
inferredcites →https://doi.org/10.1002/chem.201003388openalex-snapshot
A Novel and Convenient Synthesis of Benzonitriles: Electrophilic Cyanation of Aryl and Heteroaryl Bromides
inferredcites →https://doi.org/10.1002/chem.201303637openalex-snapshot
Copper‐Catalyzed Aromatic CH Bond Cyanation by CCN Bond Cleavage of Inert Acetonitrile
inferredcites →https://doi.org/10.1002/ejoc.201301140openalex-snapshot
Rhenium‐Catalyzed Oxidative Cyanation of Tertiary Amines with TMSCN
inferredcites →https://doi.org/10.1016/0040-4039(94)88476-5openalex-snapshot
Functionalisation including fluorination of caffeine, guanosine tetraacetate, and uridine triacetate using electrochemical oxidation
inferredcites →https://doi.org/10.1016/j.apcata.2015.03.018openalex-snapshot
PEGylated magnetic nanoparticles (PEG@Fe3O4) as cost effective alternative for oxidative cyanation of tertiary amines via C H activation
inferredcites →https://doi.org/10.1016/j.bmc.2009.11.033openalex-snapshot
Identification of triazinoindol-benzimidazolones as nanomolar inhibitors of the Mycobacterium tuberculosis enzyme TDP-6-deoxy-d-xylo-4-hexopyranosid-4-ulose 3,5-epimerase (RmlC)
inferredcites →https://doi.org/10.1016/j.cclet.2012.06.030openalex-snapshot
Indole cyanation via CH bond activation under catalysis of Ru(III)-exchanged NaY zeolite (RuY) as a recyclable catalyst
inferredcites →https://doi.org/10.1016/j.jorganchem.2004.07.034openalex-snapshot
Organometallic alkane CH activation
inferredcites →https://doi.org/10.1016/j.tet.2013.03.089openalex-snapshot
Cyanation of indoles with benzyl cyanide as the cyanide anion surrogate
inferredcites →https://doi.org/10.1016/j.tetlet.2010.04.086openalex-snapshot
Pd(OAc)2-catalyzed C–H activation of indoles: a facile synthesis of 3-cyanoindoles
inferredcites →https://doi.org/10.1016/j.tetlet.2014.01.032openalex-snapshot
Copper-mediated cyanation reactions
inferredcites →https://doi.org/10.1016/j.tetlet.2015.08.058openalex-snapshot
Direct oxidative cyanation of tertiary amines promoted by in situ generated hypervalent iodine(III)-CN intermediate
inferredcites →https://doi.org/10.1016/s0040-4020(01)91791-0openalex-snapshot
Tetrahedron report number 163
inferredcites →https://doi.org/10.1016/s1872-2067(15)60872-5openalex-snapshot
Rh(III)-catalyzed direct C–H cyanation of N-methoxybenzamides using N-cyano-N-phenyl-p-toluenesulfonamide
inferredcites →https://doi.org/10.1021/acs.joc.5b00142openalex-snapshot
Rhodium Catalyzed C2-Selective Cyanation of Indoles and Pyrroles
inferredcites →https://doi.org/10.1021/acs.joc.5b01419openalex-snapshot
Cu-Catalyzed Cyanation of Indoles with Acetonitrile as a Cyano Source
inferredcites →https://doi.org/10.1021/acs.joc.5b01666openalex-snapshot
Rhodium(III)-Catalyzed Direct Cyanation of Aromatic C–H Bond to Form 2‑(Alkylamino)benzonitriles Using N ‑Nitroso As Directing Group
inferredcites →https://doi.org/10.1021/acs.orglett.5b00886openalex-snapshot
Acetonitrile as a Cyanating Reagent: Cu-Catalyzed Cyanation of Arenes
inferredcites →https://doi.org/10.1021/acs.orglett.5b01746openalex-snapshot
Rhodium-Catalyzed Cyanation of C(sp2)–H Bond of Alkenes
inferredcites →https://doi.org/10.1021/acscatal.5b00443openalex-snapshot
Mechanism and Origins of Selectivities in the Copper-Catalyzed Dearomatization-Induced ortho C–H Cyanation of Vinylarenes
inferredcites →https://doi.org/10.1021/ar000209hopenalex-snapshot
Catalytic Functionalization of Arenes and Alkanes via C−H Bond Activation
inferredcites →https://doi.org/10.1021/ar200190gopenalex-snapshot
Rhodium Catalyzed Chelation-Assisted C–H Bond Functionalization Reactions
inferredcites →https://doi.org/10.1021/cr00087a004openalex-snapshot
Radical reactions of arenediazonium ions: An easy entry into the chemistry of the aryl radical
inferredcites →https://doi.org/10.1021/cr0104330openalex-snapshot
Ru-, Rh-, and Pd-Catalyzed C−C Bond Formation Involving C−H Activation and Addition on Unsaturated Substrates: Reactions and Mechanistic Aspects
inferredcites →https://doi.org/10.1021/ja0390303openalex-snapshot
Aerobic Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Sodium Cyanide
inferredcites →https://doi.org/10.1021/ja061715qopenalex-snapshot
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O 2 as an Oxidant
inferredcites →https://doi.org/10.1021/ja104917topenalex-snapshot
A New Combined Source of “CN” from N,N-Dimethylformamide and Ammonia in the Palladium-Catalyzed Cyanation of Aryl C−H Bonds
inferredcites →https://doi.org/10.1021/ja109617yopenalex-snapshot
Tropylium Ion Mediated α-Cyanation of Amines
inferredcites →https://doi.org/10.1021/ja204063zopenalex-snapshot
Direct Transformation of N , N -Dimethylformamide to −CN: Pd-Catalyzed Cyanation of Heteroarenes via C–H Functionalization
inferredcites →https://doi.org/10.1021/ja211389gopenalex-snapshot
Copper-Mediated Sequential Cyanation of Aryl C–B and Arene C–H Bonds Using Ammonium Iodide and DMF
inferredcites →https://doi.org/10.1021/ja405742yopenalex-snapshot
Rhodium-Catalyzed Directed C–H Cyanation of Arenes with N- Cyano- N -phenyl- p -toluenesulfonamide
inferredcites →https://doi.org/10.1021/ja511011mopenalex-snapshot
Co(III)-Catalyzed C–H Activation/Formal S N -Type Reactions: Selective and Efficient Cyanation, Halogenation, and Allylation
inferredcites →https://doi.org/10.1021/ja8017362openalex-snapshot
Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Molecular Oxygen or Hydrogen Peroxide and Sodium Cyanide: sp3 C−H Bond Activation and Carbon−Carbon Bond Formation
inferredcites →https://doi.org/10.1021/jm200587fopenalex-snapshot
Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/jm900251aopenalex-snapshot
Design and Synthesis of Small Molecule Glycerol 3-Phosphate Acyltransferase Inhibitors
inferredcites →https://doi.org/10.1021/jo00360a044openalex-snapshot
[2-(Trimethylsilyl)ethoxy]methyl (SEM) as a novel and effective imidazole and fused aromatic imidazole protecting group
inferredcites →https://doi.org/10.1021/jo061820iopenalex-snapshot
Direct Cyanation of Heteroaromatic Compounds Mediated by Hypervalent Iodine(III) Reagents: In Situ Generation of PhI(III)−CN Species and Their Cyano Transfer
inferredcites →https://doi.org/10.1021/jo4014904openalex-snapshot
Copper-Mediated Direct C2-Cyanation of Indoles Using Acetonitrile as the Cyanide Source
inferredcites →https://doi.org/10.1021/jo500087gopenalex-snapshot
Rhodium-Catalyzed Direct C–H Bond Cyanation of Arenes with Isocyanide
inferredcites →https://doi.org/10.1021/jo901583ropenalex-snapshot
Selective Functionalization of sp3 C−H Bonds Adjacent to Nitrogen Using (Diacetoxyiodo)benzene (DIB)
inferredcites →https://doi.org/10.1021/jo902185copenalex-snapshot
Chelation-Assisted Palladium-Catalyzed Cascade Bromination/Cyanation Reaction of 2-Arylpyridine and 1-Arylpyrazole C−H Bonds
inferredcites →https://doi.org/10.1021/ol0476826openalex-snapshot
Novel and Direct Oxidative Cyanation Reactions of Heteroaromatic Compounds Mediated by A Hypervalent Iodine(III) Reagent
inferredcites →https://doi.org/10.1021/ol1000439openalex-snapshot
Palladium-Catalyzed Direct Cyanation of Indoles with K 4 [Fe(CN) 6 ]
inferredcites →https://doi.org/10.1021/ol100772uopenalex-snapshot
Copper-Catalyzed Cyanation of Heterocycle Carbon−Hydrogen Bonds
inferredcites →https://doi.org/10.1021/ol201376vopenalex-snapshot
Eosin Y Catalyzed Visible Light Oxidative C–C and C–P bond Formation
inferredcites →https://doi.org/10.1021/ol202335popenalex-snapshot
Lewis Acid Catalyzed Direct Cyanation of Indoles and Pyrroles with N -Cyano- N -phenyl- p -toluenesulfonamide (NCTS)
inferredcites →https://doi.org/10.1021/ol202659eopenalex-snapshot
Photochemically Induced Radical Transformation of C(sp3)–H Bonds to C(sp3)–CN Bonds
inferredcites →https://doi.org/10.1021/ol302070topenalex-snapshot
Palladium-Assisted Regioselective C–H Cyanation of Heteroarenes Using Isonitrile as Cyanide Source
inferredcites →https://doi.org/10.1021/ol302372popenalex-snapshot
Palladium-Catalyzed C(sp2)–H Cyanation Using Tertiary Amine Derived Isocyanide as a Cyano Source
inferredcites →https://doi.org/10.1021/ol401404yopenalex-snapshot
Copper-Mediated Direct Aryl C–H Cyanation with Azobisisobutyronitrile via a Free-Radical Pathway
inferredcites →https://doi.org/10.1021/ol402201copenalex-snapshot
Rhodium Catalyzed Cyanation of Chelation Assisted C–H Bonds
inferredcites →https://doi.org/10.1021/ol402863gopenalex-snapshot
Copper-Catalyzed C–H Cyanation of Terminal Alkynes with Cyanogen Iodide
inferredcites →https://doi.org/10.1021/ol503680dopenalex-snapshot
Cobalt-Catalyzed C–H Cyanation of (Hetero)arenes and 6-Arylpurines with N -Cyanosuccinimide as a New Cyanating Agent
inferredcites →https://doi.org/10.1021/ol9017529openalex-snapshot
Chelation-Assisted Palladium-Catalyzed Direct Cyanation of 2-Arylpyridine C−H Bonds
inferredcites →https://doi.org/10.1021/om970842fopenalex-snapshot
Nitrile-Group Transfer from Solvents to Aryl Halides. Novel Carbon−Carbon Bond Formation and Cleavage Mediated by Palladium and Zinc Species
inferredcites →https://doi.org/10.1039/b820402kopenalex-snapshot
An efficient aerobic oxidative cyanation of tertiary amines with sodium cyanide using vanadium based systems as catalysts
inferredcites →https://doi.org/10.1039/b910548dopenalex-snapshot
Iron catalyzed oxidative cyanation of tertiary amines
inferredcites →https://doi.org/10.1039/c0cc03844jopenalex-snapshot
Gold-complexes catalyzed oxidative α-cyanation of tertiary amines
inferredcites →https://doi.org/10.1039/c1cc11603gopenalex-snapshot
The palladium-catalyzed cyanation of indole C–H bonds with the combination of NH4HCO3 and DMSO as a safe cyanide source
inferredcites →https://doi.org/10.1039/c1cs15004aopenalex-snapshot
Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles
inferredcites →https://doi.org/10.1039/c1ob06466eopenalex-snapshot
C–H functionalization of tertiary amines by cross dehydrogenative coupling reactions: solvent-free synthesis of α-aminonitriles and β-nitroamines under aerobic condition
inferredcites →https://doi.org/10.1039/c2cc35046gopenalex-snapshot
Copper-catalyzed cyanation of arenes using benzyl nitrile as a cyanide anion surrogate
inferredcites →https://doi.org/10.1039/c2cs15281aopenalex-snapshot
C–C, C–O and C–N bond formation via rhodium(iii)-catalyzed oxidative C–H activation
inferredcites →https://doi.org/10.1039/c2ob25875gopenalex-snapshot
Synthesis and antitumor activity of α-aminophosphonates containing thiazole[5,4-b]pyridine moiety
inferredcites →https://doi.org/10.1039/c2ra20770bopenalex-snapshot
Palladium-catalyzed cyanide metathesis: utilization of benzyl cyanide as an operator-benign reagent for aryl halide cyanations
inferredcites →https://doi.org/10.1039/c3cc49502gopenalex-snapshot
Versatile ruthenium(ii)-catalyzed C–H cyanations of benzamides
inferredcites →https://doi.org/10.1039/c3ta14783eopenalex-snapshot
A TiO2 immobilized Ru(ii) polyazine complex: a visible-light active photoredox catalyst for oxidative cyanation of tertiary amines
inferredcites →https://doi.org/10.1039/c4cc09790dopenalex-snapshot
Rhodium( iii )-catalyzed cyanation of vinylic C–H bonds: N -cyano- N -phenyl- p -toluenesulfonamide as a cyanation reagent
inferredcites →https://doi.org/10.1039/c4ob01736fopenalex-snapshot
Rhodium-catalyzed ortho-cyanation of symmetrical azobenzenes with N-cyano-N-phenyl-p-toluenesulfonamide
inferredcites →https://doi.org/10.1039/c5cc05895copenalex-snapshot
Magnetic graphitic carbon nitride: its application in the C–H activation of amines
inferredcites →https://doi.org/10.1039/c5nj00585jopenalex-snapshot
A Pd( ii )/Mg–La mixed oxide catalyst for cyanation of aryl C–H bonds and tandem Suzuki–cyanation reactions
inferredcites →https://doi.org/10.1039/jr9490001034openalex-snapshot
221. Cyanamides. Part I. The synthesis of substituted arylsulphonylcyanamides
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638. Cyanamides. Part II. The influence of substituents in the synthesis of arylsulphonylarylcyanamides
inferredcites →https://doi.org/10.1055/s-0031-1289883openalex-snapshot
Iron-Mediated Cyanation of Methoxybenzene, Indole, and 2-Arylpyridine C-H Bonds
inferredcites →https://doi.org/10.1055/s-0032-1317191openalex-snapshot
Copper-Catalyzed Oxidative Cyanation of Aryl Halides with Nitriles Involving Carbon–Carbon Cleavage
inferredcites →https://doi.org/10.1055/s-1988-27609openalex-snapshot
Cyanogen Bromide-Dimethylaminopyridine (CAP): A Convenient Source ofPositive Cyanidefor the Synthesis of 2-Cyanoimidazoles
inferredcites →https://doi.org/10.1055/s-2005-861849openalex-snapshot
Preparation of Cyanopyridines by Direct Cyanation
inferredcites →https://doi.org/10.1246/cl.2011.330openalex-snapshot
Renaissance of Organic Synthesis Using Isocyanides
inferredcites →https://doi.org/10.3998/ark.5550190.p008.682openalex-snapshot
Copper-catalyzed, oxidative sp2 C-H cyanation: facile synthesis of aromatic carbonitriles
inferredcites →https://doi.org/10.6023/cjoc1107281openalex-snapshot
Recent Progress in the Research of the Transition-Metal-Catalyzed C—CN Bonds Coupling Reactions
inferredcites →https://doi.org/10.6023/cjoc201212033openalex-snapshot
Recent Progress in the Research of Transition-Metal-Catalyzed C—CN Bond Cleavage
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Organometallic Chelation‐Assisted C − H Functionalization
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inferred← citeshttps://doi.org/10.1002/anie.201713109openalex-snapshot
Mechanochemical Activation of Iron Cyano Complexes: A Prebiotic Impact Scenario for the Synthesis of α‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201807455openalex-snapshot
Site‐Selective Remote Radical C−H Functionalization of Unactivated C−H Bonds in Amides Using Sulfone Reagents
inferred← citeshttps://doi.org/10.1002/anie.201807735openalex-snapshot
Straightforward α‐Amino Nitrile Synthesis Through Mo(CO)6‐Catalyzed Reductive Functionalization of Carboxamides
inferred← citeshttps://doi.org/10.1002/anie.201809411openalex-snapshot
Catalytic Promiscuity of Galactose Oxidase: A Mild Synthesis of Nitriles from Alcohols, Air, and Ammonia
inferred← citeshttps://doi.org/10.1002/anie.202010735openalex-snapshot
Synthesis of Nitrile Bearing Acyclic Quaternary Centers through Co(III)‐Catalyzed Sequential C−H Bond Addition to Dienes and N‐Cyanosuccinimide
inferred← citeshttps://doi.org/10.1002/anie.202108352openalex-snapshot
Electrochemical Synthesis of Glycine from Oxalic Acid and Nitrate
inferred← citeshttps://doi.org/10.1002/anie.202412552openalex-snapshot
6‐Hydroxy Picolinohydrazides Promoted Cu(I)‐Catalyzed Hydroxylation Reaction in Water: Machine‐Learning Accelerated Ligands Design and Reaction Optimization
inferred← citeshttps://doi.org/10.1002/anie.202414689openalex-snapshot
Nickel‐Catalyzed Reductive Hydrolysis of Nitriles to Alcohols
inferred← citeshttps://doi.org/10.1002/aoc.4107openalex-snapshot
Immobilization of nickel ions onto the magnetic nanocomposite based on cross‐linked melamine groups: Effective heterogeneous catalyst for N ‐Arylation of Arylboronic acids
inferred← citeshttps://doi.org/10.1002/aoc.6340openalex-snapshot
Recent advances in the rhodium‐catalyzed cyanation reactions
inferred← citeshttps://doi.org/10.1002/asia.202001219openalex-snapshot
Co(III), Rh(III) & Ir(III)‐Catalyzed Direct C−H Alkylation/Alkenylation/Arylation with Carbene Precursors
inferred← citeshttps://doi.org/10.1002/asia.70176openalex-snapshot
Recent Advances in the Synthesis of Nitrile Compounds Utilizing K 4 [Fe(CN) 6 ]: Mechanistic Studies and Applications
inferred← citeshttps://doi.org/10.1002/asia.71005openalex-snapshot
Precise Introduction of Small Functional Group (NH 2 , OH, CH 3 , CN, F, CF 3 ) in Organic Molecules via Direct C–H Activation
inferred← citeshttps://doi.org/10.1002/cctc.70947openalex-snapshot
Manganese‐Catalyzed Selective Hydration of Nitriles to Primary Amides: Experimental and Theoretical Studies
inferred← citeshttps://doi.org/10.1002/chem.201604621openalex-snapshot
Synergistic Heterobimetallic Manifold for Expedient Manganese(I)‐Catalyzed C−H Cyanation
inferred← citeshttps://doi.org/10.1002/chem.201703931openalex-snapshot
C−H Cyanation of 6‐Ring N‐Containing Heteroaromatics
inferred← citeshttps://doi.org/10.1002/chem.201704178openalex-snapshot
Pd‐Catalyzed Cyanation of (Hetero)Aryl Halides by Using Biphosphine Ligands
inferred← citeshttps://doi.org/10.1002/chem.201801746openalex-snapshot
C(sp 3 )−H Cyanation Promoted by Visible‐Light Photoredox/Phosphate Hybrid Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202001368openalex-snapshot
Para ‐Selective Cyanation of Arenes by H‐Bonded Template
inferred← citeshttps://doi.org/10.1002/chem.202300217openalex-snapshot
Iron‐Catalyzed Deoxynitrogenation of Carboxylic Acids with Cyanamides to Access Nitriles
inferred← citeshttps://doi.org/10.1002/chem.202302620openalex-snapshot
Late‐Stage C−H Activation of Drug (Derivative) Molecules with Pd(ll) Catalysis
inferred← citeshttps://doi.org/10.1002/chem.202502629openalex-snapshot
Efficient, Functional Group‐Tolerant, and Catalyst‐Free Nitrile Formation from Aldehydes
inferred← citeshttps://doi.org/10.1002/chin.201645215openalex-snapshot
ChemInform Abstract: Advances in C—CN Bond Formation via C—H Bond Activation
inferred← citeshttps://doi.org/10.1002/cjoc.201800334openalex-snapshot
Copper‐Mediated Cyanation of Aryl C—H Bond with Removable Bidenate Auxiliary Using Acetonitrile as the Cyano Source
inferred← citeshttps://doi.org/10.1002/ejoc.201700383openalex-snapshot
SeO2‐Mediated One‐Pot Synthesis of 3‐Cyanofurans from 3‐Oxo‐3‐arylpropanenitriles and Substituted Acetaldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201700546openalex-snapshot
Amides as Weak Coordinating Groups in Proximal C–H Bond Activation
inferred← citeshttps://doi.org/10.1002/ejoc.201701476openalex-snapshot
Rhodium‐Catalyzed ortho‐Cyanation of 2‐Aryl‐1,2,3‐triazole: An Alternative Approach to Suvorexant
inferred← citeshttps://doi.org/10.1002/ejoc.201900909openalex-snapshot
An Insight into Nitromethane as an Organic Nitrile Alternative Source towards the Synthesis of Aryl Nitriles
inferred← citeshttps://doi.org/10.1002/ejoc.201901364openalex-snapshot
Decyanative Cross‐Coupling of Cyanopyrimidines with O‐, S‐, and N‐Nucleophiles: A Route to Alkoxylpyrimidines, Aminopyrimidines and Alkylthiopyrimidines
inferred← citeshttps://doi.org/10.1002/ejoc.202100348openalex-snapshot
Electrochemical Oxidative C−H Cyanation of Quinoxalin‐2(1H)‐ones with TMSCN
inferred← citeshttps://doi.org/10.1002/ejoc.202301135openalex-snapshot
Three‐Component Reactions of 2,2,2‐Trifluoroethyl Ketones, Aryl Azides and Aqueous Ammonia for the Synthesis of 4‐Cyano‐1,2,3‐triazoles
inferred← citeshttps://doi.org/10.1002/jlcr.3630openalex-snapshot
New trends and applications in cyanation isotope chemistry
inferred← citeshttps://doi.org/10.1002/slct.202500936openalex-snapshot
NiFeB Hydroxide with Modulated Active Sites for Electrocatalytic Benzylamine Oxidation
inferred← citeshttps://doi.org/10.1002/smll.202411523openalex-snapshot
Unlocking Efficient Electrosynthesis of α‐Amino Acids: Adsorption Geometry Modulation and Electronic Structure Reconstruction in the Ag/Cu Bimetallic System
inferred← citeshttps://doi.org/10.1002/smll.73507openalex-snapshot
Synergistic Defect and Hole Engineering in K–Doped Cyano–Rich Porous Graphitic Carbon Nitride to Boost Photocatalytic Hydrogen Peroxide Production
inferred← citeshttps://doi.org/10.1002/tcr.202000066openalex-snapshot
‐Aminonitriles: From Sustainable Preparation to Applications in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/tcr.202200228openalex-snapshot
1,3‐Diynes: A Versatile Precursor in Transition‐Metal Catalyzed (Mediated) C−H Functionalizations
inferred← citeshttps://doi.org/10.1007/s10562-021-03779-2openalex-snapshot
Zinc Oxide/Graphene Oxide as a Robust Active Catalyst for Direct Oxidative Synthesis of Nitriles from Alcohols in Water
inferred← citeshttps://doi.org/10.1007/s11426-023-1653-3openalex-snapshot
Dual ligands relay-promoted transformation of unstrained ketones to polyfluoroarenes and nitriles
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.04.018openalex-snapshot
Transition-metal-switchable divergent synthesis of nitrile-containing pyrazolo[1,5-a]pyridines and indolizines
inferred← citeshttps://doi.org/10.1016/j.chempr.2018.09.027openalex-snapshot
Palladium-Catalyzed Late-Stage Direct Arene Cyanation
inferred← citeshttps://doi.org/10.1016/j.jcat.2021.01.003openalex-snapshot
Iron-catalyzed reductive strecker reaction
inferred← citeshttps://doi.org/10.1016/j.jechem.2022.02.054openalex-snapshot
Recent developments in electrosynthesis of nitriles and electrocatalytic cyanations
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111313openalex-snapshot
Facile dehydration of primary amides to nitriles catalyzed by lead salts: The anionic ligand matters
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112576openalex-snapshot
Hemin-catalyzed controlled oxidative cyanation of secondary amine for the synthesis of α-aminonitriles and α-iminonitriles
inferred← citeshttps://doi.org/10.1016/j.molliq.2019.112157openalex-snapshot
Metal-based surface active ionic liquids: Self-assembling characteristics and C C bond functionalization of tertiary amines with TMSCN in aqueous micellar solutions
inferred← citeshttps://doi.org/10.1016/j.tet.2018.01.005openalex-snapshot
Strecker reaction and α-amino nitriles: Recent advances in their chemistry, synthesis, and biological properties
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131388openalex-snapshot
RETRACTED: Metal-catalyzed cyanation of aromatic hydrocarbon with less toxic nitriles as a cyano source
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132313openalex-snapshot
Primary amides: Sustainable weakly coordinating groups in transition metal-catalyzed C–H bond functionalization reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.07.030openalex-snapshot
Redox-neutral C–H cyanation of tetrahydroisoquinolines under photoredox catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153062openalex-snapshot
KSeCN as an efficient cyanide source for the one-step synthesis of imino-1-oxoisoindolines via copper-promoted C–H activation
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00507openalex-snapshot
3d Transition Metals for C–H Activation
inferred← citeshttps://doi.org/10.1021/acs.jcim.4c02136openalex-snapshot
Mechanisms of C(sp3)-H Functionalization of Acetonitrile or Acetone with Alkynes: A DFT Investigation
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01386openalex-snapshot
Rh(III)-Catalyzed C–H Cyanation of 2H-Indazole with N-Cyano-N-phenyl-p-toluenesulfonamide
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02642openalex-snapshot
Iron-Catalyzed α-C–H Cyanation of Simple and Complex Tertiary Amines
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03026openalex-snapshot
Electrochemical Oxidative Regioselective C–H Cyanation of Imidazo[1,2- a ]pyridines
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01631openalex-snapshot
Construction of CF3-Functionalized Fully Substituted Benzonitriles through Rauhut–Currier Reaction Initiated [3 + 3] Benzannulation
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02498openalex-snapshot
Synthesis of Unsymmetrical Diarylfumaronitriles via Tandem Michael Addition and Oxidation under K3Fe(CN)6/O2 System
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02835openalex-snapshot
KOtBu-Mediated Reductive Cyanation of Tertiary Amides for Synthesis of α-Aminonitriles
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01703openalex-snapshot
Intermolecular C–H Aminocyanation of Indoles via Copper–iodine Cocatalyzed Tandem C–N/C–C Bond Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02050openalex-snapshot
Chemoselective α-Alkylation and α-Olefination of Arylacetonitriles with Alcohols via Iron-Catalyzed Borrowing Hydrogen and Dehydrogenative Coupling
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01431openalex-snapshot
Palladium-Catalyzed Direct C(sp2)–H Cyanomethylation of Arylamides using Chloroacetonitrile
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02085openalex-snapshot
Visible Light-Enhanced [3 + 2] Cycloaddition of N,N-Disubstituted Hydrazines with Organo-Cyanamides: Access to Polysubstituted 1,2,4-Triazol-3-amines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00281openalex-snapshot
Metal-Free Cyanation of gem-Difluoroalkenes via Azide-Mediated C–C Double Bond Fragmentation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02945openalex-snapshot
An Acetic Acid-Promoted Strecker Type Reaction of N,N-Disubstituted Aminomalononitriles: An Efficient Way for the Construction of α-Aminonitriles
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02731openalex-snapshot
Palladium-Catalyzed, ortho-Selective C–H Halogenation of Benzyl Nitriles, Aryl Weinreb Amides, and Anilides
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03036openalex-snapshot
Rhodium-Catalyzed Direct Bis-cyanation of Arylimidazo[1,2-α]pyridine via Double C–H Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00578openalex-snapshot
Pd-Catalyzed Cyclization and Cyanation of Alkynone O -Methyloximes with tert -Butyl Isocyanide
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01169openalex-snapshot
Photoinduced Nickel-Catalyzed Cascade Cyclization and Cyanation of Functionalized Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02021openalex-snapshot
Metal-Free Aerobic Oxidative Cyanation of Tertiary Amines: Azobis(isobutyronitrile) (AIBN) as a Sole Cyanide Source
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02133openalex-snapshot
Access to Cyano-Containing Isoxazolines via Copper-Catalyzed Domino Cyclization/Cyanation of Alkenyl Oximes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01763openalex-snapshot
Nickel-Catalyzed Cyanation of Benzylic and Allylic Pivalate Esters
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02191openalex-snapshot
Metal-Free Regioselective Monocyanation of Hydroxy-, Alkoxy-, and Benzyloxyarenes by Potassium Thiocyanate and Silica Sulfuric Acid as a Cyanating Agent
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01194openalex-snapshot
Synthesis of 2-Arylbenzothiazole and 2-Arylthiazole Derivatives via a Ru-Catalyzed meta-Selective C–H Nitration Reaction
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b02529openalex-snapshot
Mechanistic Investigations of Aluminum Nitrite Assisted Aryl Nitrile Synthesis through C(sp3)–C(sp2) Bond Cleavage of Aryl Ketones
inferred← citeshttps://doi.org/10.1021/acs.oprd.7b00285openalex-snapshot
Copper-Mediated C–X Functionalization of Aryl Halides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03138openalex-snapshot
Combined Cyanoborylation, C–H Activation Strategy for Styrene Functionalization
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00468openalex-snapshot
Ni-Catalyzed C–H Cyanation of (Hetero)arenes with 2-Cyanoisothiazolidine 1,1-Dioxide as a Cyanation Reagent
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01867openalex-snapshot
Synthesis of Diverse γ-Lactams via Rh-Catalyzed C(sp 2 )–H Addition to Aliphatic Nitriles
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01897openalex-snapshot
Paired Electrolysis for Decarboxylative Cyanation: 4-CN-Pyridine, a Versatile Nitrile Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c04185openalex-snapshot
Fe-Catalyzed Direct Synthesis of Nitriles from Carboxylic Acids with Electron-Deficient N -Cyano- N -aryl–arylsulfonamide
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02256openalex-snapshot
Ag-Catalyzed Cyanomethylation of Amines Using Nitromethane as a C1 Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00429openalex-snapshot
Palladium-Catalyzed Directed Carbon–Carbon Bond Activation of Aryl Nitriles for Cyano Transfer
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02552openalex-snapshot
Electrochemically Driven Denitrative Cyanation of Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03901openalex-snapshot
Formal 1,1-Hydrocyanation Reaction of Alkynyl Halides with Isocyanides Enabled by Dual Nickel/Base Catalysis Relay
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02286openalex-snapshot
Rh(III)-Catalyzed Atroposelective C–H Cyanation of 1-Aryl benzo[ h ]isoquinolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04508openalex-snapshot
Co(III)-Catalyzed Three-Component Cascade for the Synthesis of α-Quaternary Acyclic Nitriles via C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00892openalex-snapshot
Chemodivergent C–H Activation and C–C Coupling between Indoles and Alkyne-Tethered N -Cyanosulfonamides via Substrate-Controlled Group Migration
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02869openalex-snapshot
Electrochemical One- or Two-Electron Oxidation Enables Chemoselective α-Amino C(sp3)–H Arylation and Cyanation
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00826openalex-snapshot
Iminoxyl Radical-Promoted Oxycyanation and Aminocyanation of Unactivated Alkenes: Synthesis of Cyano-Featured Isoxazolines and Cyclic Nitrones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01199openalex-snapshot
Decarbonylative Cyanation of Amides by Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01710openalex-snapshot
Deoxycyanamidation of Alcohols with N -Cyano- N -phenyl- p -methylbenzenesulfonamide (NCTS)
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01756openalex-snapshot
Catalytic Asymmetric Electrophilic Cyanation of 3-Substituted Oxindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03858openalex-snapshot
Oxycyanation of Vinyl Ethers with 2,2,6,6-Tetramethyl-N-oxopiperidinium Enabled by Electron Donor–Acceptor Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02225openalex-snapshot
Synthesis and Reactivity of N -Allenyl Cyanamides
inferred← citeshttps://doi.org/10.1021/acscatal.1c00733openalex-snapshot
A Molecular Iron-Based System for Divergent Bond Activation: Controlling the Reactivity of Aldehydes
inferred← citeshttps://doi.org/10.1021/acscatal.2c01029openalex-snapshot
Nickel-Catalyzed Synthesis of an Aryl Nitrile via Aryl Exchange between an Aromatic Amide and a Simple Nitrile
inferred← citeshttps://doi.org/10.1021/acscatal.5c03331openalex-snapshot
Pd-Catalyzed Late-Stage Installation of Nitrile and Carbamoyl Groups via a Cross-Coupling Approach of Thianthrenium Salts with Isonitriles
inferred← citeshttps://doi.org/10.1021/acscatal.7b03583openalex-snapshot
Advances in Direct Metal-Catalyzed Functionalization of Azobenzenes
inferred← citeshttps://doi.org/10.1021/acscatal.8b00021openalex-snapshot
Direct Synthesis of N,N-Dimethylated and β-Methyl N,N-Dimethylated Amines from Nitriles Using Methanol: Experimental and Computational Studies
inferred← citeshttps://doi.org/10.1021/acscatal.8b05111openalex-snapshot
Ni-Mediated Generation of “CN” Unit from Formamide and Its Catalysis in the Cyanation Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.9b03916openalex-snapshot
Atom-Economical and Tandem Conversion of Nitriles to N -Methylated Amides Using Methanol and Water
inferred← citeshttps://doi.org/10.1021/acscatal.9b04586openalex-snapshot
Nickel-Catalyzed Cyanation of Aryl Halides and Hydrocyanation of Alkynes via C–CN Bond Cleavage and Cyano Transfer
inferred← citeshttps://doi.org/10.1021/jacs.4c00885openalex-snapshot
Highly Stable 72-Nuclearity Nanocages for Efficient Synthesis of Aryl Nitriles via Ni/Cu Synergistic Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.5c11876openalex-snapshot
Electrophilic Cyanation with Carbon Isotopes: A Versatile Access to 13 C, 14 C, and 11 C Aryl Nitriles from Labeled NCTS
inferred← citeshttps://doi.org/10.1021/jacs.8b00643openalex-snapshot
Mechanistic Insight Facilitates Discovery of a Mild and Efficient Copper-Catalyzed Dehydration of Primary Amides to Nitriles Using Hydrosilanes
inferred← citeshttps://doi.org/10.1021/jacs.8b01330openalex-snapshot
Palladium and Lewis-Acid-Catalyzed Intramolecular Aminocyanation of Alkenes: Scope, Mechanism, and Stereoselective Alkene Difunctionalizations
inferred← citeshttps://doi.org/10.1021/jacsau.2c00030openalex-snapshot
Late-Stage Carbon-14 Labeling and Isotope Exchange: Emerging Opportunities and Future Challenges
inferred← citeshttps://doi.org/10.1021/jacsau.5c00633openalex-snapshot
Enantioselective Radical Hydrocyanoalkylation of Alkenes via Photoenzymatic Catalysis
inferred← citeshttps://doi.org/10.1039/c6cc08601bopenalex-snapshot
CuI-Catalyzed intramolecular aminocyanation of terminal alkynes in N-(2-ethynylphenyl)-N-sulfonylcyanamides via Cu–vinylidene intermediates
inferred← citeshttps://doi.org/10.1039/c6sc04907aopenalex-snapshot
Room temperature decarboxylative cyanation of carboxylic acids using photoredox catalysis and cyanobenziodoxolones: a divergent mechanism compared to alkynylation
inferred← citeshttps://doi.org/10.1039/c7ra02574bopenalex-snapshot
Palladium( ii )-catalyzed ortho-C–H olefination of phenylalanine and phenylethylamine derivatives directed by removable picolinamide group
inferred← citeshttps://doi.org/10.1039/c8cc08930bopenalex-snapshot
Rhodium( iii )-catalyzed aromatic C–H cyanation with dimethylmalononitrile as a cyanating agent
inferred← citeshttps://doi.org/10.1039/c8ob01770kopenalex-snapshot
Recent developments and applications of cyanamides in electrophilic cyanation
inferred← citeshttps://doi.org/10.1039/c8ob02140fopenalex-snapshot
Non-toxic cyanide sources and cyanating agents
inferred← citeshttps://doi.org/10.1039/c8ob02186dopenalex-snapshot
A facile tandem decyanation/cyanation reaction of α-iminonitriles toward cyano-substituted amides
inferred← citeshttps://doi.org/10.1039/c8qo01143eopenalex-snapshot
Cyanofluorination of vinyl ethers enabled by electron donor–acceptor complexes
inferred← citeshttps://doi.org/10.1039/c9cy01170fopenalex-snapshot
Application of metal oxide semiconductors in light-driven organic transformations
inferred← citeshttps://doi.org/10.1039/c9gc00720bopenalex-snapshot
Strecker reactions with hexacyanoferrates as non-toxic cyanide sources
inferred← citeshttps://doi.org/10.1039/c9nj00776hopenalex-snapshot
Cu(OAc) 2 -Mediated benzimidazole-directed C–H cyanation using 2-(4-methylpiperazin-1-yl)acetonitrile as the cyano source
inferred← citeshttps://doi.org/10.1039/c9ob02760bopenalex-snapshot
Tandem transformations and multicomponent reactions utilizing alcohols following dehydrogenation strategy
inferred← citeshttps://doi.org/10.1039/c9qo00235aopenalex-snapshot
Copper-catalysed C(sp 3 )–N coupling initiated by selective C–C bond cleavage of cyclobutanone oxime esters
inferred← citeshttps://doi.org/10.1039/c9qo01055fopenalex-snapshot
Transition-metal-free direct C-3 cyanation of quinoxalin-2(1 H )-ones with ammonium thiocyanate as the “CN” source
inferred← citeshttps://doi.org/10.1039/c9ra02979fopenalex-snapshot
One-pot regioselective C–H activation iodination–cyanation of 2,4-diarylquinazolines using malononitrile as a cyano source
inferred← citeshttps://doi.org/10.1039/c9ra06120gopenalex-snapshot
Oxidative cyanation of N -aryltetrahydroisoquinoline induced by visible light for the synthesis of α-aminonitrile using potassium thiocyanate as a “CN” agent
inferred← citeshttps://doi.org/10.1039/d0cs00535eopenalex-snapshot
Beyond classical sulfone chemistry: metal- and photocatalytic approaches for C–S bond functionalization of sulfones
inferred← citeshttps://doi.org/10.1039/d0cy02087gopenalex-snapshot
Recent advances and perspectives in manganese-catalyzed C–H activation
inferred← citeshttps://doi.org/10.1039/d0gc00608dopenalex-snapshot
Base-mediated benzannulation of α-cyanocrotonates with ynones: facile synthesis of benzonitriles and fluorenes
inferred← citeshttps://doi.org/10.1039/d0nj01996hopenalex-snapshot
Recent advances in C–CN and C–H bond activation of green nitrile (MeCN) for organo-complexation, cyanation and cyanomethylation
inferred← citeshttps://doi.org/10.1039/d0ob00485eopenalex-snapshot
The palladium-catalyzed direct C3-cyanation of indoles using acetonitrile as the cyanide source
inferred← citeshttps://doi.org/10.1039/d0ob01928copenalex-snapshot
An aerobic and green C–H cyanation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/d0ob02309dopenalex-snapshot
Recent advances in Rh( iii )/Ir( iii )-catalyzed C–H functionalization/annulation via carbene migratory insertion
inferred← citeshttps://doi.org/10.1039/d0qo00282hopenalex-snapshot
Access to cyano-substituted pyrazolines through copper-catalyzed cascade cyanation/cyclization of unactivated olefins
inferred← citeshttps://doi.org/10.1039/d0qo01182gopenalex-snapshot
Visible light-mediated applications of methylene blue in organic synthesis
inferred← citeshttps://doi.org/10.1039/d0ra01286fopenalex-snapshot
Direct cyanation, hydrocyanation, dicyanation and cyanofunctionalization of alkynes
inferred← citeshttps://doi.org/10.1039/d1cy00241dopenalex-snapshot
Directing group strategies in catalytic sp 2 C–H cyanations: scope, mechanism and limitations
inferred← citeshttps://doi.org/10.1039/d1ob00192bopenalex-snapshot
Cyanoalkylation/alkynylation of allylic alcohol through intramolecular radical 1,2-alkynyl migration
inferred← citeshttps://doi.org/10.1039/d1ob00675dopenalex-snapshot
Recent developments in decarboxylative C(aryl)–X bond formation from (hetero)aryl carboxylic acids
inferred← citeshttps://doi.org/10.1039/d1ob01086gopenalex-snapshot
An expedient route to tricyanovinylindoles and indolylmaleimides from o -alkynylanilines utilising DMSO as a one-carbon synthon
inferred← citeshttps://doi.org/10.1039/d1ob02143eopenalex-snapshot
Metal-free three-component cyanoalkylation of quinoxalin-2(1 H )-ones with vinylarenes and azobis(alkylcarbonitrile)s
inferred← citeshttps://doi.org/10.1039/d1qo01858bopenalex-snapshot
Cyanation and cyanomethylation of trimethylammonium salts via electrochemical cleavage of C–N bonds
inferred← citeshttps://doi.org/10.1039/d2cc00342bopenalex-snapshot
Palladium-catalyzed synthesis of nitriles from N -phthaloyl hydrazones
inferred← citeshttps://doi.org/10.1039/d2cc05826jopenalex-snapshot
Organo-cyanamides: convenient reagents for catalytic amidation of carboxylic acids
inferred← citeshttps://doi.org/10.1039/d2cs00012aopenalex-snapshot
C–H bond activation and sequential addition to two different coupling partners: a versatile approach to molecular complexity
inferred← citeshttps://doi.org/10.1039/d2nj06338gopenalex-snapshot
Metal-free synthesis of ketonitriles via C–F bond cleavage
inferred← citeshttps://doi.org/10.1039/d2ob01199aopenalex-snapshot
Iron( iii )-catalyzed α-cyanation and carbonylation with 2-pyridylacetonitrile: divergent synthesis of α-amino nitriles and tetrahydroisoquinolinones
inferred← citeshttps://doi.org/10.1039/d2ob01644copenalex-snapshot
Iodonium ylides: an emerging and alternative carbene precursor for C–H functionalizations
inferred← citeshttps://doi.org/10.1039/d2qo00486kopenalex-snapshot
Copper-catalyzed regioselective 1,4-sulfonylcyanation of 1,3-enynes with sulfonyl chlorides and TMSCN
inferred← citeshttps://doi.org/10.1039/d3cc03075jopenalex-snapshot
Weakly coordinating tert -amide assisted Rh( iii )-catalyzed C4-cyanation of indoles: application in photophysical studies
inferred← citeshttps://doi.org/10.1039/d3cc05880hopenalex-snapshot
Cyanation with isocyanides: recent advances and perspectives
inferred← citeshttps://doi.org/10.1039/d3ob01528aopenalex-snapshot
tert -Butylhydroperoxide mediated radical cyanoalkylation/cyanoalkenylation of 2-anilino-1,4-naphthoquinones with vinylarenes/arylalkynes and azobis(alkylcarbonitrile)s
inferred← citeshttps://doi.org/10.1039/d4cc04539dopenalex-snapshot
Deacetylative cyanation: a cyanide-free route to thiocyanates and cyanamides
inferred← citeshttps://doi.org/10.1039/d4ce00950aopenalex-snapshot
Bridging linker installation strategy in the engineering of copper( ii ) complexes: activation of nitriles, efficient catalysts for the cyanosilylation of aldehydes
inferred← citeshttps://doi.org/10.1039/d4ob01849dopenalex-snapshot
TFA-catalyzed solvent-free dearomative cyanidation of isoquinoline using (Boc) 2 O as an acylation agent
inferred← citeshttps://doi.org/10.1039/d5ob00012bopenalex-snapshot
Catalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile: access to isobutyronitrile containing diarylmethanes
inferred← citeshttps://doi.org/10.1039/d5qo01254fopenalex-snapshot
Copper-catalyzed radical aminocyanation of allenes
inferred← citeshttps://doi.org/10.1039/d6cc00754fopenalex-snapshot
Desulfonylcyanamidation of α,β-unsaturated sulfones with N -tosyl N -aryl cyanamides (NCTS): access to N -cyanoenaminones
inferred← citeshttps://doi.org/10.1055/a-1704-4822openalex-snapshot
Synthesis of C3-Cyanomethylated Imidazo[1,2-a]pyridines via Ultrasound-Promoted Three-Component Reaction under Catalyst- and Oxidant-Free Conditions
inferred← citeshttps://doi.org/10.1055/a-1965-3028openalex-snapshot
Recent Advances on Radical-Mediated Cyanoalkylation/Cyanation using AIBN and Analogues as the Radical Sources
inferred← citeshttps://doi.org/10.1055/a-2053-1750openalex-snapshot
Silver-Catalyzed Synthesis of Nitriles from Carboxylic Acids and Cyanamides
inferred← citeshttps://doi.org/10.1055/s-0037-1610795openalex-snapshot
Copper-Mediated Direct Aromatic ortho-C–H Cyanation by AIBN
inferred← citeshttps://doi.org/10.1080/00268976.2022.2105271openalex-snapshot
DFT investigates the mechanisms of cross-dehydrogenative coupling between heterocycles and acetonitrile
inferred← citeshttps://doi.org/10.1080/00397911.2019.1655765openalex-snapshot
Cp*Co(III) catalyzed annulation of N-Cbz hydrazones for the redox-neutral synthesis of isoquinolines via C–H/N–N bond activation
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