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Synthesis of Symmetric 1,4-Diamino-2-Butynes via a Cu(I)-Catalyzed One-Pot A3-Coupling/Decarboxylative Coupling of a Propiolic Acid, an Aldehyde, and an Amine

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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.201100608openalex-snapshot
Synthesis of Oxazolidin‐2‐ones via a Copper(I)‐Catalyzed Tandem Decarboxylative/Carboxylative Cyclization of a Propiolic Acid, a Primary Amine and an Aldehyde
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New Approaches for Decarboxylative Biaryl Coupling
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Carboxylic Acids as Substrates in Homogeneous Catalysis
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Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
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Concise and Diversity‐Oriented Route toward Polysubstituted 2‐Aminoimidazole Alkaloids and Their Analogues
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Synthesis of α‐Aryl Nitriles through Palladium‐Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates
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Carboxylic Acids as Traceless Directing Groups for Formal meta ‐Selective Direct Arylation
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Palladium‐Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
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Synthesis of Enantiomerically Enriched Propargylamines by Copper‐Catalyzed Addition of Alkynes to Enamines
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Dienyne Ring‐Closing Metathesis Approach for the Construction of Taxosteroids
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Rhodium(I)‐Catalysed Intramolecular [2+2+2] Cyclotrimerisations of 15‐, 20‐ and 25‐Membered Azamacrocycles: Experimental and Theoretical Mechanistic Studies
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Synthesis of Aryl Sulfides by Decarboxylative CS Cross‐Couplings
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Chemodivergent Metathesis of Dienynes Catalyzed by Ruthenium–Indenylidene Complexes: An Experimental and Computational Study
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The Aromatic Carbon–Carbon ipso‐Substitution Reaction
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Copper(I)‐Catalyzed Deacetylenative Coupling of Propargylic Amines: An Efficient Synthesis of Symmetric 1,4‐Diamino‐2‐butynes
inferredcites →https://doi.org/10.1016/j.tetlet.2011.02.009openalex-snapshot
One-pot synthesis of 1,4-diarylsubstituted 1,3-diynes from the sequential coupling reactions of aryl iodides and propiolic acid
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Inhibition of bovine plasma amine oxidase by 1,4-diamino-2-butenes and -2-butynes
inferredcites →https://doi.org/10.1021/cr1002744openalex-snapshot
Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions
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Acceleration of Conjugated Dienyne Cycloaromatization
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Reactions of an allylic sulfide, sulfoxide, and sulfone with singlet oxygen. The observation of a remarkable diastereoselective oxidation
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Group-Selective Ring-Closing Enyne Metathesis: Concentration-Dependent Selectivity Profile of Alkynylsilyloxy-Tethered Dienynes
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On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes
inferredcites →https://doi.org/10.1021/ja105245fopenalex-snapshot
Room Temperature Palladium-Catalyzed Decarboxylative ortho-Acylation of Acetanilides with α-Oxocarboxylic Acids
inferredcites →https://doi.org/10.1021/ja107103bopenalex-snapshot
Palladium-Catalyzed Decarboxylative Couplings of 2-(2-Azaaryl)acetates with Aryl Halides and Triflates
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Palladium-Catalyzed Intramolecular Direct Arylation of Benzoic Acids by Tandem Decarboxylation/C−H Activation
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Theoretical Analysis of Factors Controlling Pd-Catalyzed Decarboxylative Coupling of Carboxylic Acids with Olefins
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Nontraditional Reactions of Azomethine Ylides: Decarboxylative Three-Component Couplings of α-Amino Acids
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Bis(methoxycarbonyl)sulfur diimide, a convenient reagent for the allylic amination of alkenes
inferredcites →https://doi.org/10.1021/jo101398aopenalex-snapshot
Synthesis of Symmetrical and Unsymmetrical Diarylalkynes from Propiolic Acid Using Palladium-Catalyzed Decarboxylative Coupling
inferredcites →https://doi.org/10.1021/jo102175fopenalex-snapshot
Pd/PR3-Catalyzed Cross-Coupling of Aromatic Carboxylic Acids with Electron-Deficient Polyfluoroarenes via Combination of Decarboxylation with sp2 C−H Cleavage
inferredcites →https://doi.org/10.1021/jo102218vopenalex-snapshot
Brønsted Acid-Catalyzed Decarboxylative Redox Amination: Formation of N-Alkylindoles from Azomethine Ylides by Isomerization
inferredcites →https://doi.org/10.1021/jo2013725openalex-snapshot
Microwave-Assisted Decarboxylative Three-Component Coupling of a 2-Oxoacetic Acid, an Amine, and an Alkyne
inferredcites →https://doi.org/10.1021/jo802290ropenalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Aryl Halides
inferredcites →https://doi.org/10.1021/jo9519219openalex-snapshot
Highly Enantioselective Intramolecular Cyclopropanation Reactions of N-Allylic-N-methyldiazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxamidates
inferredcites →https://doi.org/10.1021/ol070708jopenalex-snapshot
Synthesis of the Tricyclic Core of Colchicine via a Dienyne Tandem Ring-Closing Metathesis Reaction
inferredcites →https://doi.org/10.1021/ol1004615openalex-snapshot
Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling
inferredcites →https://doi.org/10.1021/ol100752yopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol703130yopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol9002509openalex-snapshot
Chemoselective C−H Bond Activation: Ligand and Solvent Free Iron-Catalyzed Oxidative C−C Cross-Coupling of Tertiary Amines with Terminal Alkynes. Reaction Scope and Mechanism
inferredcites →https://doi.org/10.1021/ol901129vopenalex-snapshot
A Novel Iron-Catalyzed Decarboxylative Csp3−Csp2 Coupling of Proline Derivatives and Naphthol
inferredcites →https://doi.org/10.1038/nature07046openalex-snapshot
The total synthesis of (-)-cyanthiwigin F by means of double catalytic enantioselective alkylation
inferredcites →https://doi.org/10.1039/c0cc03772aopenalex-snapshot
Copper-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with aryl halides
inferredcites →https://doi.org/10.1039/c1cs15093fopenalex-snapshot
Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
inferredcites →https://doi.org/10.1073/pnas.1015268108openalex-snapshot
Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb17333.xopenalex-snapshot
1,4–Diamino‐2‐butyne as the mechanism‐based pea diamine oxidase inhibitor
inferredcites →https://doi.org/10.1126/science.1128684openalex-snapshot
Synthesis of Biaryls via Catalytic Decarboxylative Coupling

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Nhc-Silver Complexes as Effective Catalysts for the Synthesis of Propiolic Acids by Reaction of Alkynes with Co2
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Redox‐Neutral Copper(II) Carboxylate Catalyzed α‐Alkynylation of Amines
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Altering Copper‐Catalyzed A3 Couplings by Mechanochemistry: One‐Pot Synthesis of 1,4‐Diamino‐2‐butynes from Aldehydes, Amines, and Calcium Carbide
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Redox‐Neutral Copper(II) Carboxylate Catalyzed α‐Alkynylation of Amines
inferred← citeshttps://doi.org/10.1002/anie.201805505openalex-snapshot
Altering Copper‐Catalyzed A3 Couplings by Mechanochemistry: One‐Pot Synthesis of 1,4‐Diamino‐2‐butynes from Aldehydes, Amines, and Calcium Carbide
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Double A3‐Coupling of Primary Amines Catalysed by Gold Complexes
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ChemInform Abstract: Synthesis of Symmetric 1,4‐Diamino‐2‐butynes via a Cu(I)‐Catalyzed One‐Pot A3‐Coupling/Decarboxylative Coupling of a Propiolic Acid, an Aldehyde, and an Amine.
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Copper(I)‐Catalyzed Decarboxylative Coupling of Propiolic Acids with Secondary Amines and Aldehydes
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Nano‐Fe3O4@TiO2/Cu2O Core‐shell Composite: A Convenient Magnetic Separable Catalyst for A3 and KA2 Coupling
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Decarboxylative A3 ‐coupling reactions: An overview
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Decarboxylative dipropargylation of primary amines with propiolic acids and formaldehyde via metal-free coupling
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Nickel-catalyzed decarboxylative coupling reaction of alkynyl carboxylic acids and allyl acetates
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Cu-catalyzed decarboxylative coupling of propiolic acids with boronic acids
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Copper-catalyzed decarboxylative coupling reactions for the synthesis of propargyl amines
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CuI/CuBr2-catalyzed decarboxylative/A3 reaction of propiolic acids for the facile synthesis of 1,4-diheterocycle-2-butynes
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