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Cu-Catalyzed Aerobic Oxidative Three-Component Coupling Route to N -Sulfonyl Amidines via an Ynamine Intermediate
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.200900004openalex-snapshot
Copper‐Catalyzed N‐Arylation/Hydroamin(d)ation Domino Synthesis of Indoles and its Application to the Preparation of a Chek1/KDR Kinase Inhibitor Pharmacophore
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Practical Synthesis of Amides from In Situ Generated Copper( I ) Acetylides and Sulfonyl Azides
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Domino Cu‐Catalyzed CN Coupling/Hydroamidation: A Highly Efficient Synthesis of Nitrogen Heterocycles
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CH Functionalization/CN Bond Formation: Copper‐Catalyzed Synthesis of Benzimidazoles from Amidines
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Copper‐Mediated Coupling of 1,1‐Dibromo‐1‐alkenes with Nitrogen Nucleophiles: A General Method for the Synthesis of Ynamides
inferredcites →https://doi.org/10.1002/anie.200905817openalex-snapshot
Ynamides: Versatile Tools in Organic Synthesis
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Copper‐Catalyzed Oxidative Cross‐Coupling of Sulfoximines and Alkynes
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Amine‐Free Approach toward N‐Toluenesulfonyl Amidine Construction: A Phosphite‐Mediated Beckmann‐Like Coupling of Oximes and p‐Toluenesulfonyl Azide
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Gold(I)‐Catalyzed Aminohalogenation of Fluorinated N′‐Aryl‐N‐Propargyl Amidines for the Synthesis of Imidazole Derivatives under Mild Conditions
inferredcites →https://doi.org/10.1002/ejoc.200900143openalex-snapshot
Catalyzed Imidation of Tertiary Amines by Simple Copper Salts
inferredcites →https://doi.org/10.1002/ejoc.201200383openalex-snapshot
Recent Highlights in Ketenimine Chemistry
inferredcites →https://doi.org/10.1016/0010-8545(94)80059-6openalex-snapshot
The coordination chemistry of the amidine ligand
inferredcites →https://doi.org/10.1016/j.bmcl.2009.11.104openalex-snapshot
Synthesis and SAR of sulfonyl- and phosphoryl amidine compounds as anti-resorptive agents
inferredcites →https://doi.org/10.1016/j.tetlet.2010.11.135openalex-snapshot
Formation of N-sulfonylamidines by copper-catalyzed coupling of sulfonyl azides, terminal alkynes, and trialkylamines
inferredcites →https://doi.org/10.1016/s0040-4039(00)75383-4openalex-snapshot
A novel synthesis of ynamines. Copper catalyzed oxidation of phenylacetylene in the presence of secondary amines
inferredcites →https://doi.org/10.1016/s0079-6468(08)70378-3openalex-snapshot
5 Amidines and Guanidines in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/cr100003sopenalex-snapshot
Ynamides: A Modern Functional Group for the New Millennium
inferredcites →https://doi.org/10.1021/ic4012229openalex-snapshot
Porous Metal–Organic Framework Catalyzing the Three-Component Coupling of Sulfonyl Azide, Alkyne, and Amine
inferredcites →https://doi.org/10.1021/ja0432968openalex-snapshot
Highly Efficient One-Pot Synthesis of N -Sulfonylamidines by Cu-Catalyzed Three-Component Coupling of Sulfonyl Azide, Alkyne, and Amine
inferredcites →https://doi.org/10.1021/ja056399eopenalex-snapshot
Copper-Catalyzed Hydrative Amide Synthesis with Terminal Alkyne, Sulfonyl Azide, and Water
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Anti-Markovnikov Addition of Both Primary and Secondary Amines to Terminal Alkynes Catalyzed by the TpRh(C2H4)2/PPh3 System
inferredcites →https://doi.org/10.1021/ja077406xopenalex-snapshot
Copper-Catalyzed Aerobic Oxidative Amidation of Terminal Alkynes: Efficient Synthesis of Ynamides
inferredcites →https://doi.org/10.1021/ja2120629openalex-snapshot
Copper-Catalyzed Aerobic [3+2]-Annulation of N-Alkenyl Amidines
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Copper-Catalyzed Aerobic Aliphatic C–H Oxygenation Directed by an Amidine Moiety
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An Unexpected Diethyl Azodicarboxylate-Promoted Dehydrogenation of Tertiaryamine and Tandem Reaction with Sulfonyl Azide
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Discovery of Novel STAT3 Small Molecule Inhibitors via in Silico Site-Directed Fragment-Based Drug Design
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N-Allyl-N-sulfonyl Ynamides as Synthetic Precursors to Amidines and Vinylogous Amidines. An Unexpected N-to-C 1,3-Sulfonyl Shift in Nitrile Synthesis
inferredcites →https://doi.org/10.1021/jo800733popenalex-snapshot
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
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Synthetic Utility of Ammonium Salts in a Cu-Catalyzed Three-Component Reaction as a Facile Coupling Partner
inferredcites →https://doi.org/10.1021/ol060056jopenalex-snapshot
A Facile Access to N -Sulfonylimidates and Their Synthetic Utility for the Transformation to Amidines and Amides
inferredcites →https://doi.org/10.1021/ol1000236openalex-snapshot
CuCl/CCl4-Promoted Convenient Synthesis of Sulfonyl Amidines from Tertiary Amines and Sulfonyl Azides
inferredcites →https://doi.org/10.1021/ol1004615openalex-snapshot
Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling
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Copper-Catalyzed Synthesis of Quinoxalines with o-Phenylenediamine and Terminal Alkyne in the Presence of Bases
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Direct Condensation of Sulfonamide and Formamide: NaI-Catalyzed Synthesis ofN-Sulfonyl Formamidine Using TBHP as Oxidant
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Copper-Catalyzed Oxidative Alkynylation of Diaryl Imines with Terminal Alkynes: A Facile Synthesis of Ynimines
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Total Synthesis of an Oxepine Natural Product, (±)-Janoxepin
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Palladium-Catalyzed N-Monoarylation of Amidines and a One-Pot Synthesis of Quinazoline Derivatives
inferredcites →https://doi.org/10.1021/ol303023yopenalex-snapshot
Three-Component Reaction of Propargyl Amines, Sulfonyl Azides, and Alkynes: One-Pot Synthesis of Tetrasubstituted Imidazoles
inferredcites →https://doi.org/10.1021/ol400099hopenalex-snapshot
Palladium-Catalyzed Trifluoroethylation of Terminal Alkynes with 1,1,1-Trifluoro-2-iodoethane
inferredcites →https://doi.org/10.1021/ol400560mopenalex-snapshot
Copper-Catalyzed Oxidative Diamination of Terminal Alkynes by Amidines: Synthesis of 1,2,4-Trisubstituted Imidazoles
inferredcites →https://doi.org/10.1021/ol802844zopenalex-snapshot
Synthesis of Amidines Using N-Allyl Ynamides. A Palladium-Catalyzed Allyl Transfer through an Ynamido−π-Allyl Complex
inferredcites →https://doi.org/10.1021/ol901831sopenalex-snapshot
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inferredcites →https://doi.org/10.1039/b314707jopenalex-snapshot
Structural diversity in the coordination of amidines and guanidines to monovalent metal halides
inferredcites →https://doi.org/10.1039/b910009aopenalex-snapshot
Facile synthesis of sulfonyl amidines via carbon–nitrogen bond formation mediated by FeCl3
inferredcites →https://doi.org/10.1039/c1cc14640hopenalex-snapshot
Direct use of dioxygen as an oxygen source: catalytic oxidative synthesis of amides
inferredcites →https://doi.org/10.1039/c3gc40797gopenalex-snapshot
Metal- and solvent-free synthesis of N-sulfonylformamidines
inferredcites →https://doi.org/10.1055/s-0033-1340287openalex-snapshot
Synthesis of N-Sulfonylamidines by Catalyst-Free Hydroamination of Ynamides and Amines
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The C=C Bond Decomposition Initiated by Enamine‐Azide Cycloaddition for Catalyst‐ and Additive‐Free Synthesis of N‐Sulfonyl Amidines
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Mechanochemical Metal‐free N‐Sulfonyl Transfer Reaction: Expedient Synthesis of N‐Sulfonyl Amidines
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A Comprehensive Review of Recent Synthetic Strategies and Functionalization of Amidines
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Tandem Coupling of Azide with Isonitrile and Boronic Acid: Facile Access to Functionalized Amidines
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Tandem Coupling of Azide with Isonitrile and Boronic Acid: Facile Access to Functionalized Amidines
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Cu(I)@Fe3O4 nanoparticles supported on imidazolium‐based ionic liquid‐grafted cellulose: Green and efficient nanocatalyst for multicomponent synthesis of N‐sulfonylamidines and N‐sulfonylacrylamidines
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ChemInform Abstract: Cu‐Catalyzed Aerobic Oxidative Three‐Component Coupling Route to N‐Sulfonyl Amidines via an Ynamine Intermediate.
inferred← citeshttps://doi.org/10.1002/ejoc.201501092openalex-snapshot
Base‐Induced One‐Pot Preparation of N‐ or P‐Substituted Alkynes
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Air‐Assisted 2‐Oxo‐Driven Dehydrogenative α,α‐Diamination of 2‐Oxo Aldehydes to 2‐Oxo Acetamidines
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Air‐Induced One‐Pot Synthesis of N‐Sulfonylformamidines from Sulfonyl Chlorides, NaN3, and Tertiary/Secondary Amines
inferred← citeshttps://doi.org/10.1002/ejoc.202400776openalex-snapshot
Metal‐Free Direct Synthesis of N‐Sulfonyl Amidines from Thioamides and Electron Deficient N‐Sulfonylamides
inferred← citeshttps://doi.org/10.1002/ejoc.202500400openalex-snapshot
Amidine Syntheses from Classic to Contemporary for Medicinal Lead Compounds and Natural Products
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Supported NHC-Benzimi@Cu Complex as a Magnetically Separable and Reusable Catalyst for the Multicomponent and Click Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via Huisgen 1,3-Dipolar Cycloaddition
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One-pot multicomponent synthesis of N-sulfonyl amidines using magnetic separable nanoparticles-decorated N-heterocyclic carbene complex with copper
inferred← citeshttps://doi.org/10.1007/s11426-023-1739-yopenalex-snapshot
Copper-catalyzed C(sp)–H aryl amination enables modular synthesis of quinolines and 2-quinolinones
inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00070-2openalex-snapshot
Guanidinate, Amidinate, and Formamidinate Ligands
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Recent Advances in Amidines and Their Modern Synthetic Methodologies
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Catalytic C(sp)-H carboxylation with CO2
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Iron oxide (Fe3O4) magnetic nanoparticles supported on wrinkled fibrous nanosilica (WFNS) functionalized by biimidazole ionic liquid as an effective and reusable heterogeneous magnetic nanocatalyst for the efficient synthesis of N-sulfonylamidines
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Antimicrobial activity of new benzazolyl N-sulfonyl amidines
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An inexpensive, metal-free and one-pot approach towards N-sulfonyl amidines: Identification of a chorismate mutase inhibitor with activities against S. aureus
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Mukaiyama reagent-promoted metal-free preparation of alkynyl sulfones and phosphonates under mild conditions
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Recent trends in the chemistry of triflamides
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Copper-catalyzed the coupling reaction of sulfonylazides with formamides for the synthesis of N-sulfonyl amidines
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TCT promoted efficient synthesis of N-sulfonyl (form)amidines from sulfonamides and (form)amides
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N-Sulfonyl amidine synthesis via three-component coupling reaction using heterogeneous copper catalyst derived from metal-organic frameworks
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Three-component synthesis of N-sulfonylformamidines in the presence of magnetic cellulose supported N-heterocyclic carbene-copper complex, as an efficient heterogeneous nanocatalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.10.027openalex-snapshot
Three component reaction of aryl diazonium salt with sulfonamide & actonitrile to synthesize N-sulfonyl amidine
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Isoquinoline Kelch-like ECH-Associated Protein 1-Nuclear Factor (Erythroid-Derived 2)-like 2 (KEAP1-NRF2) Inhibitors with High Metabolic Stability
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Synthesis of (Z)-β-Chloro-enamides via a Base-Promoted trans-Hydroamidation of Alkynyl Chlorides Using 1,1-Dichloroalkenes as Precursor
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Metal-Free Direct Access toN-Sulfonyl Amidines from Sulfonamides and Secondary Amines Involving Tandem C–N Bond Formations
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Amine-Induced Selective C–C Bond Cleavage of 2,2,2-Trifluoroethyl Carbonyls for the Synthesis of Ureas and Amides
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Microwave-Assisted Copper-Catalyzed Four-Component Tandem Synthesis of 3-N-Sulfonylamidine Coumarins
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Peptidines: glycine-amidine-based oligomers for solution- and solid-phase synthesis
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Potentially antibreast cancer enamidines via azide–alkyne–amine coupling and their molecular docking studies
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Copper-catalyzed aerobic oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines: direct access to construct quinoxalines
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N -Sulfonyl acetylketenimine as a highly reactive intermediate for the synthesis of N -sulfonyl amidines
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Electrochemically generated N -iodoaminium species as key intermediates for selective methyl sulphonylimination of tertiary amines
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Visible-light enabled room-temperature dealkylative imidation of secondary and tertiary amines promoted by aerobic ruthenium catalysis
inferred← citeshttps://doi.org/10.1039/d1qo00063bopenalex-snapshot
Catalytic synthesis of functionalized amidines via cobalt-carbene radical coupling with isocyanides and amines
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Metal-free synthesis of N -sulfonylformamidines via skeletal reconstruction of sulfonyl oximonitriles
inferred← citeshttps://doi.org/10.1039/d1ra00772fopenalex-snapshot
Catalyst-free one-pot, four-component approach for the synthesis of di- and tri-substituted N -sulfonyl formamidines
inferred← citeshttps://doi.org/10.1039/d3cc05977dopenalex-snapshot
Olefin skeletal rearrangement enabling access to multiarylated N -sulfonyl amidines
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Radical revelations: the pnictogen effect in linear acetylenes
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Green synthesis of N -sulfonyl amidine using a CuI-incorporated CoFe 2 O 4 nano-catalyst in aqueous medium
inferred← citeshttps://doi.org/10.1039/d4nj02051kopenalex-snapshot
Vicinal difunctionalization of nitriles: modular construction of N -alkyl amidines and late-stage modification
inferred← citeshttps://doi.org/10.1039/d4ob00804aopenalex-snapshot
Reactions of alkynes with C–S bond formation: recent developments
inferred← citeshttps://doi.org/10.1039/d5ob01072aopenalex-snapshot
Synthesis of N -sulfonyl acetamidines using calcium carbide as an alkyne source
inferred← citeshttps://doi.org/10.1039/d5qo01010aopenalex-snapshot
Highly stereoselective synthesis of N -sulfonyl amidines with calcium carbide as an acetylene source
inferred← citeshttps://doi.org/10.1134/s107042801902009xopenalex-snapshot
Three-Component Reaction of Sulfonamides with Acetylene and Amines
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One-pot synthesis of propynoates and propynenitriles
inferred← citeshttps://doi.org/10.3390/inorganics12110283openalex-snapshot
Catalytic Behavior of NHC–Silver Complexes in the Carboxylation of Terminal Alkynes with CO2
inferred← citeshttps://doi.org/10.3762/bjoc.16.243openalex-snapshot
Regioselective synthesis of heterocyclic N-sulfonyl amidines from heteroaromatic thioamides and sulfonyl azides
inferred← citeshttps://doi.org/10.3987/com-15-13307openalex-snapshot
Facile One-Pot Synthesis of Cyclic N-Sulfonylamidines from Lactam and Sulfonamide
inferred← citeshttps://doi.org/10.6023/cjoc202106035openalex-snapshot
Copper-Catalyzed Regioselective C(sp3)—H Sulfonimidization of Aliphatic Cyclic Tertiary Amines
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Réactions de transfert de nitrènes catalysées par des complexes de fer : de la compréhension des mécanismes au développement de réactions multi-séquentielles
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Développement de ligands anticlastogéniques des prohibitines
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