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Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Aryl Halides

https://doi.org/10.1021/jo802290r
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471212466openalex-snapshot
Handbook of Organopalladium Chemistry for Organic Synthesis
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Acetylenic Coupling: A Powerful Tool in Molecular Construction
inferredcites →https://doi.org/10.1002/9783527619535openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions
inferredcites →https://doi.org/10.1002/adsc.200606135openalex-snapshot
Poly(norbornene)‐Supported N‐Heterocyclic Carbenes as Ligands in Catalysis
inferredcites →https://doi.org/10.1002/anie.200390273openalex-snapshot
A Versatile Catalyst for the Sonogashira Coupling of Aryl Chlorides
inferredcites →https://doi.org/10.1002/anie.200500368openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling Reactions in Total Synthesis
inferredcites →https://doi.org/10.1002/anie.200502017openalex-snapshot
General Catalysts for the Suzuki–Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water
inferredcites →https://doi.org/10.1002/anie.200700022openalex-snapshot
PtCl2‐Catalyzed Hydrative Cyclization of Trialkyne Functionalities to Form Bicyclic Spiro Ketones
inferredcites →https://doi.org/10.1002/anie.200701991openalex-snapshot
Live‐Cell‐Permeable Poly(p‐phenylene ethynylene)
inferredcites →https://doi.org/10.1002/anie.200702931openalex-snapshot
Platinum‐Catalyzed Formation of Cyclic‐Ketone‐Fused Indoles from N‐(2‐Alkynylphenyl)lactams
inferredcites →https://doi.org/10.1002/chem.200800301openalex-snapshot
Highly Convenient Amine‐Free Sonogashira Coupling in Air in a Polar Mixed Aqueous Medium by trans‐ and cis‐[(NHC)2PdX2] (X=Cl, Br) Complexes of N/O‐Functionalized N‐Heterocyclic Carbenes
inferredcites →https://doi.org/10.1002/chin.200502088openalex-snapshot
Catalytic Efficiency of a New Tridentate Ferrocenyl Phosphine Auxiliary: Sonogashira Cross‐Coupling Reactions of Alkynes with Aryl Bromides and Chlorides at Low Catalyst Loadings of 10‐1 to 10‐4 mol %.
inferredcites →https://doi.org/10.1016/0040-4020(95)00677-zopenalex-snapshot
Palladium-catalyzed arylation of polar organometallics mediated by 9-methoxy-9-borabicyclo[3.3.1]nonane: Suzuki reactions of extended scope
inferredcites →https://doi.org/10.1016/0040-4039(80)80120-1openalex-snapshot
Carboncarbon bond formation by cross-coupling of enol phosphates with organoaluminium compounds catalyzed by palladium(O) complex
inferredcites →https://doi.org/10.1016/0040-4039(96)00517-5openalex-snapshot
Enantioposition-selective alkynylation of biaryl ditriflates by palladium-catalyzed asymmetric cross-coupling
inferredcites →https://doi.org/10.1016/0957-4166(96)00408-9openalex-snapshot
Synthesis of an optically active poly(aryleneethynylene) containing extended conjugation in the repeat unit
inferredcites →https://doi.org/10.1016/j.bmcl.2007.12.045openalex-snapshot
Photoactivated enediynes as targeted antitumoral agents: Efficient routes to antibody and gold nanoparticle conjugates
inferredcites →https://doi.org/10.1016/j.tet.2004.12.026openalex-snapshot
Amine- and phosphine-free palladium(II)-catalyzed homocoupling reaction of terminal alkynes
inferredcites →https://doi.org/10.1016/j.tet.2006.01.001openalex-snapshot
Copper-free Sonogashira reaction using 7-chloro camptothecins
inferredcites →https://doi.org/10.1016/j.tet.2008.05.100openalex-snapshot
Development of a one-pot sequential Sonogashira coupling for the synthesis of benzofurans
inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.092openalex-snapshot
Sonogashira cross-coupling reactions of aryl chlorides with alkynes catalysed by a tetraphosphine–palladium catalyst
inferredcites →https://doi.org/10.1016/j.tetlet.2005.12.025openalex-snapshot
Microwave enhanced cross-coupling reactions involving alkenyl- and alkynyltrifluoroborates
inferredcites →https://doi.org/10.1016/j.tetlet.2006.03.015openalex-snapshot
A copper-free Sonogashira reaction using a Pd/MgLa mixed oxide
inferredcites →https://doi.org/10.1016/j.tetlet.2006.10.156openalex-snapshot
Facile access to 4-(1-alkynyl)-2(5H)-furanones by Sonogashira coupling of terminal acetylenes with β-tetronic acid bromide: efficient synthesis of cleviolide
inferredcites →https://doi.org/10.1016/j.tetlet.2007.07.207openalex-snapshot
Copper-free PdCl2/PPh3-catalyzed Sonogashira coupling reaction of aryl bromides with terminal alkynes in water
inferredcites →https://doi.org/10.1016/j.tetlet.2007.08.015openalex-snapshot
Copper-free Sonogashira cross-coupling reaction catalyzed by polymer-supported N-heterocyclic carbene palladium complex
inferredcites →https://doi.org/10.1016/j.tetlet.2008.01.080openalex-snapshot
Novel 5-(oligofluorenyl)-1,10-phenanthroline type ligands: synthesis, linear and two-photon absorption properties
inferredcites →https://doi.org/10.1016/s0022-328x(02)01158-0openalex-snapshot
Development of Pd–Cu catalyzed cross-coupling of terminal acetylenes with sp2-carbon halides
inferredcites →https://doi.org/10.1016/s0040-4039(00)01543-4openalex-snapshot
Efficient coupling reactions of lithium alkynyl(triisopropoxy)borates with aryl halides: application to the antifungal terbinafine synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)91094-3openalex-snapshot
A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
inferredcites →https://doi.org/10.1016/s0040-4039(01)00811-5openalex-snapshot
Pd-catalyzed cross-coupling of alkynylsilanols with iodobenzenes
inferredcites →https://doi.org/10.1016/s0040-4039(01)85081-4openalex-snapshot
An efficient stereospecific synthesis of olefins by the palladium-catalyzed reaction of grignard reagents with alkenyl iodides.
inferredcites →https://doi.org/10.1021/cr020377iopenalex-snapshot
Palladium-Catalyzed Alkynylation
inferredcites →https://doi.org/10.1021/ja00241a035openalex-snapshot
Stereospecific palladium-catalyzed coupling reactions of vinyl iodides with acetylenic tin reagents
inferredcites →https://doi.org/10.1021/ja004195mopenalex-snapshot
Atom-Efficient Metal-Catalyzed Cross-Coupling Reaction of Indium Organometallics with Organic Electrophiles
inferredcites →https://doi.org/10.1021/ja049758zopenalex-snapshot
Synthesis and Electronic Properties of Donor−Acceptor π-Conjugated Siloles
inferredcites →https://doi.org/10.1021/ja710564bopenalex-snapshot
Transition-Metal-Free Synthesis of Poly(phenylene Ethynylene)s with Alternating Aryl-Perfluoroaryl Units
inferredcites →https://doi.org/10.1021/jo00098a051openalex-snapshot
A Simple and Economical Synthetic Route to p-Ethynylaniline and Ethynyl-Terminated Substrates
inferredcites →https://doi.org/10.1021/jo00396a046openalex-snapshot
A general synthesis of terminal and internal arylalkynes by the palladium-catalyzed reaction of alkynylzinc reagents with aryl halides
inferredcites →https://doi.org/10.1021/jo0104532openalex-snapshot
First Total Synthesis of (−)-Ichthyothereol and Its Acetate
inferredcites →https://doi.org/10.1021/jo01047a008openalex-snapshot
The Substitution of Aryl Iodides with Cuprous Acetylides. A Synthesis of Tolanes and Heterocyclics 1
inferredcites →https://doi.org/10.1021/jo048066qopenalex-snapshot
Efficient Stille Cross-Coupling Reaction Catalyzed by the Pd(OAc)2/Dabco Catalytic System
inferredcites →https://doi.org/10.1021/jo048599zopenalex-snapshot
Copper-Free Sonogashira Coupling Reaction with PdCl2 in Water under Aerobic Conditions
inferredcites →https://doi.org/10.1021/jo049474xopenalex-snapshot
Palladium Complexes of 1,3,5,7-Tetramethyl-2,4,8-trioxa-6-phenyl-6-phosphaadamantane: Synthesis, Crystal Structure and Use in the Suzuki and Sonogashira Reactions and the α-Arylation of Ketones
inferredcites →https://doi.org/10.1021/jo051882topenalex-snapshot
Modified Palladium-Catalyzed Sonogashira Cross-Coupling Reactions under Copper-, Amine-, and Solvent-Free Conditions
inferredcites →https://doi.org/10.1021/jo0525175openalex-snapshot
Efficient Copper-Free PdCl2(PCy3)2-Catalyzed Sonogashira Coupling of Aryl Chlorides with Terminal Alkynes
inferredcites →https://doi.org/10.1021/jo061959topenalex-snapshot
Highly Emissive π-Conjugated Alkynylpyrene Oligomers: Their Synthesis and Photophysical Properties
inferredcites →https://doi.org/10.1021/jo070607zopenalex-snapshot
Synthesis and Structure-Linear and Structure-Nonlinear Optical Properties of Multi-Dipolar Zigzag Oligoaryleneethynylenes
inferredcites →https://doi.org/10.1021/ma0625915openalex-snapshot
Alkyne-Functional Polymers through Sonogashira Coupling to Poly(4-bromostyrene)
inferredcites →https://doi.org/10.1021/ol0061586openalex-snapshot
Non-Sonogashira-Type Palladium-Catalyzed Coupling Reactions of Terminal Alkynes Assisted by Silver(I) Oxide or Tetrabutylammonium Fluoride
inferredcites →https://doi.org/10.1021/ol006439dopenalex-snapshot
Suzuki−Miyaura Coupling of Alkynylboronic Esters Generated in Situ from Acetylenic Derivatives
inferredcites →https://doi.org/10.1021/ol0257732openalex-snapshot
A Copper-Free Sonogashira Coupling Reaction in Ionic Liquids and Its Application to a Microflow System for Efficient Catalyst Recycling
inferredcites →https://doi.org/10.1021/ol030017xopenalex-snapshot
Highly Selective Synthesis of (E)-3-Methyl-1-trialkylsilyl-3-en-1-ynes via trans-Selective Alkynylation Catalyzed by Cl2Pd(DPEphos) and Stereospecific Methylation with Methylzincs Catalyzed by Pd(tBu3P)2
inferredcites →https://doi.org/10.1021/ol035632fopenalex-snapshot
Efficient and General Protocol for the Copper-Free Sonogashira Coupling of Aryl Bromides at Room Temperature
inferredcites →https://doi.org/10.1021/ol047983fopenalex-snapshot
Tandem Sonogashira Coupling: An Efficient Tool for the Synthesis of Diarylalkynes
inferredcites →https://doi.org/10.1021/ol048870zopenalex-snapshot
Catalytic Efficiency of a New Tridentate Ferrocenyl Phosphine Auxiliary: Sonogashira Cross-Coupling Reactions of Alkynes with Aryl Bromides and Chlorides at Low Catalyst Loadings of 10-1 to 10-4 Mol %
inferredcites →https://doi.org/10.1021/ol703130yopenalex-snapshot
One-Pot Synthesis of Diarylalkynes Using Palladium-Catalyzed Sonogashira Reaction and Decarboxylative Coupling of sp Carbon and sp2 Carbon
inferredcites →https://doi.org/10.1021/ol801025uopenalex-snapshot
Copper-Catalyzed Sonogashira-Type Reactions Under Mild Palladium-Free Conditions
inferredcites →https://doi.org/10.1021/om060636kopenalex-snapshot
A Copper- and Amine-Free Sonogashira Reaction of Aryl Halides Catalyzed by 1,3,5-Triaza-7-phosphaadamantane Palladium Systems
inferredcites →https://doi.org/10.1055/s-1995-5220openalex-snapshot
Aryl- and Heteroaryl-Alkyne Coupling Reactions Catalyzed by Palladium on Carbon and CuI in an Aqueous Medium
inferredcites →https://doi.org/10.1055/s-2001-13390openalex-snapshot
A Highly Effective Pd/Cu-Catalyzed Coupling Reaction of Terminal Alkynes with Organic Halides Promoted by Tetrabutylammonium Fluoride or Hydroxide
inferredcites →https://doi.org/10.1246/cl.1997.1233openalex-snapshot
Cu(I)/Pd(0)-Catalyzed Cross-Coupling Reaction of Alkynylsilanes with Aryl or Alkenyl Triflates: “Sila”-Sonogashira-Hagihara 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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A Half Century of the Sonogashira Reaction
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Palladium( II ) Chloride–Tertiary Phosphine
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Palladium( II ) Chloride – Tertiary Phosphine
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Palladium( II ) Chloride – Tertiary Phosphine
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Palladium( II ) Chloride – Tertiary Phosphine
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Alkylation, Alkenylation, and Arylation of Alkynes and Allenes
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Oxidation
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Reactions Involving Elimination of CO 2 and Ketones
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Synthesis of Biaryls and Aryl Ketones via Microwave‐Assisted Decarboxylative Cross‐Couplings
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Palladium‐Catalyzed Decarboxylative sp‐sp2 Cross‐Coupling Reactions of Aryl and Vinyl Halides and Triflates with α,β‐Ynoic Acids using Silver Oxide
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Synthesis of Propiolic Acids via Copper‐Catalyzed Insertion of Carbon Dioxide into the CH Bond of Terminal Alkynes
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Synthesis of 1,4‐Diarylbuta‐1,3‐dienes through Palladium‐ Catalyzed Decarboxylative Coupling of Unsaturated Carboxylic Acids
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Synthesis of Diarylalkynes by Iron/Copper Co‐Catalyzed Decarboxylative spsp2 Coupling of Alkynyl Carboxylic Acids and Aryl Halides
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Synthesis of Oxazolidin‐2‐ones via a Copper(I)‐Catalyzed Tandem Decarboxylative/Carboxylative Cyclization of a Propiolic Acid, a Primary Amine and an Aldehyde
inferred← citeshttps://doi.org/10.1002/adsc.201100934openalex-snapshot
Carboxylation of Terminal Alkynes with Carbon Dioxide Catalyzed by Poly(N‐Heterocyclic Carbene)‐Supported Silver Nanoparticles
inferred← citeshttps://doi.org/10.1002/adsc.201200876openalex-snapshot
Phosphine‐Free Palladium‐Catalyzed Decarboxylative Coupling of Alkynylcarboxylic Acids with Aryl and Heteroaryl Halides
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Chemoselective Synthesis of Unsymmetrical Internal Alkynes or Vinyl Sulfones via Palladium‐Catalyzed Cross‐Coupling Reaction of Sodium Sulfinates with Alkynes
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Palladium‐Catalyzed Cross‐Coupling of Alkynyl Carboxylic Acids with Isocyanides: Solvent‐Controlled Selective Synthesis of 5‐Iminofuranones and 5‐Iminopyrrolones
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Metal‐Free Decarboxylative Trichlorination of Alkynyl Carboxylic Acids: Synthesis of Trichloromethyl Ketones
inferred← citeshttps://doi.org/10.1002/adsc.201701469openalex-snapshot
Silver‐catalyzed Double Decarboxylative Radical Alkynylation/Annulation of Arylpropiolic Acids with α‐keto Acids: Access to Ynones and Flavones under Mild Conditions
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Visible Light‐Catalyzed Decarboxylative Alkynylation of Arenediazonium Salts with Alkynyl Carboxylic Acids: Direct Access to Aryl Alkynes by Organic Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.70120openalex-snapshot
Palladium‐Catalyzed Denitrative Decarboxylation of Nitroarenes with Alkynyl Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/ajoc.201500227openalex-snapshot
Copper‐Catalyzed Synthesis of Amino‐Substituted Polycyclic Aromatic Hydrocarbons by the Sequential Reaction between Aryl Alkynyl Carboxylic Acids and Amines
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Copper‐Catalyzed Double Decarboxylative Coupling Reactions of Alkynyl Carboxylic Acid and Glyoxylic Acid: Synthesis of Propargyl Amines and Imidazopyridines
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Sequential One‐Pot Coupling Reactions of Diiodobenzenes, Propiolic Acid, and Aryl Halides for the Synthesis of Diarylalkynyl Arenes
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Metal‐Free Doubly Decarboxylative Three‐Component Reaction: Synthesis of Propargyl Amines
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Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
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Palladium‐Catalyzed Cascade Annulation To Construct Functionalized β‐ and γ‐Lactones in Ionic Liquids
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An Efficient Nanoscale Heterogeneous Catalyst for the Capture and Conversion of Carbon Dioxide at Ambient Pressure
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Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
inferred← citeshttps://doi.org/10.1002/anie.201403341openalex-snapshot
Palladium‐Catalyzed Cascade Annulation To Construct Functionalized β‐ and γ‐Lactones in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/anie.201409103openalex-snapshot
An Efficient Nanoscale Heterogeneous Catalyst for the Capture and Conversion of Carbon Dioxide at Ambient Pressure
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Mechanistic study of palladium‐catalyzed decarboxylative coupling of phenylpropiolic acid and aryl iodide
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Xantphos‐coordinated palladium dithiolates: Highly efficient catalyst for decarboxylative Sonogashira reaction into corresponding alkynes
inferred← citeshttps://doi.org/10.1002/bkcs.10706openalex-snapshot
Copper‐catalyzed Decarboxylative Hydroboration: Synthesis of Vinyl Boronic Esters
inferred← citeshttps://doi.org/10.1002/bkcs.12221openalex-snapshot
Palladium‐Catalyzed Decarboxylative Homodimerization of Propiolic Acids: Synthesis of 1, 3‐Enynes
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CH Carboxylation of Terminal Alkynes Catalyzed by Low Loadings of Silver(I)/DMSO at Ambient CO2 Pressure
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Carboxylation of Terminal Alkynes with Carbon Dioxide Catalyzed by an In Situ Ag2O/N‐Heterocyclic Carbene Precursor System
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Palladium‐Catalyzed Intramolecular Self‐Alkylation of Polyfluoroarene via Heck and Decarboxylation Process
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Recent Advances in Nickel‐Catalyzed Synthesis of Allenes: New Insights and Perspectives
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Decarboxylative Cross‐Dehydrogenative Coupling of Tetrahydroisoquinoline and Alkynoic Acids Using Recyclable Carbon Nanotube Supported Copper/Nickel Oxide Catalysts
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A Versatile Catalyst for Intermolecular Direct Arylation of Indoles with Benzoic Acids as Arylating Reagents
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Controlling the Dual‐Emission Character of Aryl‐Modified o‐Carboranes by Intramolecular CH⋅⋅⋅O Interaction Sites
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ChemInform Abstract: Palladium‐Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Aryl Halides.
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One‐Pot Carboboration of Alkynes Using Lithium Borylcyanocuprate and the Subsequent Suzuki–Miyaura Cross‐Coupling of the Resulting Tetrasubstituted Alkenylborane
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Phosphane‐Free Copper‐Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Halides under Aerobic Conditions
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Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides
inferred← citeshttps://doi.org/10.1002/ejoc.201200679openalex-snapshot
Copper‐Catalyzed Decarboxylative Three‐Component Reactions for the Synthesis of Imidazo[1,2‐a]pyridines
inferred← citeshttps://doi.org/10.1002/ejoc.201201606openalex-snapshot
Palladium‐Catalyzed Sonogashira Reaction for the Synthesis of Arylalkynecarboxylic Acids from Aryl Bromides at Low Temperature
inferred← citeshttps://doi.org/10.1002/ejoc.201201608openalex-snapshot
1,5,7‐Triazabicyclo[4.4.0]dec‐1‐ene‐Mediated Acetylene Dicarboxylation and Alkyne Carboxylation Using Carbon Dioxide
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Palladium‐Catalyzed Decarboxylative C–H Alkynylation of Benzoxazoles with α,β‐Ynoic Acids
inferred← citeshttps://doi.org/10.1002/ejoc.201403644openalex-snapshot
Palladium‐Catalyzed Oxidative Aminocarbonylation by Decarboxylative Coupling: Synthesis of Alkynyl Amides
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Peptide Functionalization Through the Generation of Selenocysteine Electrophile
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Decarboxylative Coupling Reactions
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Synthesis of Di‐Substituted Alkynes via Palladium‐Catalyzed Decarboxylative Coupling and C‐H Activation
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Copper‐Catalyzed Decarboxylative Cycloaddition of Alkynyl Carboxylic Acids and Sodium Azide with Epoxides and Ethers
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Decarboxylative Coupling Reactions
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Metal-Catalyzed Cross-Coupling Reactions in the Decoration of Pyridines
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Attachment at Ring Positions
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Zeolite-based copper catalyst for decarboxylative coupling of alkynyl carboxylic acids with aryl iodides
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Catalytic C(sp)-H carboxylation with CO2
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Synthesis, characterization of palladium hydroxysalen complex and its application in the coupling reaction of arylboronic acids: Mizoroki–Heck type reaction and decarboxylative couplings
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Nitrogen-doped mesoporous carbon single crystal-based Ag nanoparticles for boosting mild CO2 conversion with terminal alkynes
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Ligand-free palladium-catalyzed decarboxylative coupling reactions of aryl iodides and alkynyl carboxylic acids
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Palladium-catalyzed cross-coupling reactions of triarylbismuthanes with terminal alkynes under aerobic conditions
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Domino [Pd]-Catalysis: Heck followed by decarboxylative Sonogashira couplings under microwave irradiation in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.mcat.2017.07.015openalex-snapshot
UV-irradiation-mediated palladium nanoparticle catalytic system: Heck and decarboxylative coupling reactions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131788openalex-snapshot
Ultrasound assisted Cu-catalyzed decarbonylative Sonogashira coupling-cyclization strategy: Synthesis and evaluation of 3-heteroarylmethylene isoindolin-1-ones against SIRT1
inferred← citeshttps://doi.org/10.1016/j.solidstatesciences.2012.08.012openalex-snapshot
Ligand-based luminescence in lead-containing complexes: The effect of conjugated organic ligands on fluorescence
inferred← citeshttps://doi.org/10.1016/j.tet.2009.04.047openalex-snapshot
Pd-catalyzed decarboxylative couplings of arenecarboxylic acids with aryl iodides
inferred← citeshttps://doi.org/10.1016/j.tet.2011.06.001openalex-snapshot
Highly selective palladium-catalyzed Suzuki–Miyaura monocoupling reactions of ethene and arene derivatives bearing two or more electrophilic sites
inferred← citeshttps://doi.org/10.1016/j.tet.2012.06.003openalex-snapshot
Copper-catalyzed decarboxylative coupling of aryl halides with alkynyl carboxylic acids performed in water
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.022openalex-snapshot
Synthesis of 1,4-diarylsubstituted 1,3-diynes through ligand-free copper-catalyzed oxidative decarboxylative homocoupling of aryl propiolic acids
inferred← citeshttps://doi.org/10.1016/j.tet.2015.05.017openalex-snapshot
Copper-catalyzed direct synthesis of furans and thiophenes via decarboxylative coupling of alkynyl carboxylic acids with H2O or Na2S
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.036openalex-snapshot
Pd-catalyzed decarboxylative coupling of arylalkynyl carboxylic acids with allyl ethers: regioselective synthesis of branched 1,3-enynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.12.138openalex-snapshot
Copper-catalyzed decarboxylative cross-coupling of propiolic acids and terminal alkynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.054openalex-snapshot
Silver-catalyzed decarboxylative halogenation of carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.110openalex-snapshot
Synthesis of symmetrical diarylalkyne from palladium-catalyzed decarboxylative couplings of propiolic acid and aryl bromides under water
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.05.134openalex-snapshot
Palladium-catalyzed Sonogashira cross-coupling of organic tellurides with alkynes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.07.091openalex-snapshot
Efficient synthesis of unsymmetric diarylalkynes from decarboxylative coupling in a continuous flow reaction system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.117openalex-snapshot
Synthesis of aryl alkynyl carboxylic acids and aryl alkynes from propiolic acid and aryl halides by site selective coupling and decarboxylation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.023openalex-snapshot
Copper catalysed domino decarboxylative cross coupling-cyclisation reactions: synthesis of 2-arylindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.08.076openalex-snapshot
Ligand free palladium catalyzed decarboxylative cross-coupling of aryl halides with oxalate monoester salts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.005openalex-snapshot
Nickel-catalyzed decarboxylative coupling reaction of alkynyl carboxylic acids and allyl acetates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.118openalex-snapshot
Cu-catalyzed decarboxylative coupling of propiolic acids with boronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.05.134openalex-snapshot
Copper-catalyzed decarboxylative coupling reactions for the synthesis of propargyl amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.029openalex-snapshot
Palladium on manganese ferrite: an efficient catalyst for ligand free decarboxylative Sonogashira reaction with arene diazonium tetrafluoroborate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.029openalex-snapshot
Continuous flow reactions in water for the synthesis of propargylamines via a metal-free decarboxylative coupling reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.06.073openalex-snapshot
Palladium and copper catalyzed Sonogashira decarboxylative coupling of aryl iodides and alkynyl carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.09.054openalex-snapshot
Nickel-catalyzed oxidative decarboxylative coupling reactions between alkynyl carboxylic acids and arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.02.073openalex-snapshot
Nickel-catalyzed decarboxylative coupling of an alkynyl carboxylic acid with aryl iodides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.079openalex-snapshot
A novel tandem Pd-catalyzed intramolecular allylic decarboxylative coupling and “diradical conjugated 1,3-dien-5-yne cycloaromatization”: An unusual ortho -selectivity in the cycloaromatization and the mechanistic implications
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151231openalex-snapshot
Recent topics of gold catalyst featuring Z-type ligands
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151415openalex-snapshot
Recent advances of propiolic acids in organic reactions
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b02855openalex-snapshot
Composite System of Ag Nanoparticles and Metal–Organic Frameworks for the Capture and Conversion of Carbon Dioxide under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c02729openalex-snapshot
Metproxybicyclone, a Novel Carbocyclic Aryl-dione Acetyl-CoA Carboxylase-Inhibiting Herbicide for the Management of Sensitive and Resistant Grass Weeds
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01997openalex-snapshot
Discovery of 2-Aminopyrimidines as Potent Agonists for the Bitter Taste Receptor TAS2R14
inferred← citeshttps://doi.org/10.1021/acs.joc.2c03039openalex-snapshot
Decarbonylative Alkynylation of Aryl Anhydrides via Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02689openalex-snapshot
Electromagnetic Mill-Promoted Palladium-Catalyzed Heck-Type Cyclization/Decarboxylative Coupling of (Z)-1-Iodo-1,6-diene with Propiolic Acids
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02361openalex-snapshot
Synthesis of Terminal Allenes via a Copper-Catalyzed Decarboxylative Coupling Reaction of Alkynyl Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00830openalex-snapshot
Decarboxylative Alkynyl Termination of Palladium-Catalyzed Catellani Reaction: A Facile Synthesis of α-Alkynyl Anilines via Ortho C–H Amination and Alkynylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02155openalex-snapshot
Silver-Catalyzed Decarboxylative Azidation of Aliphatic Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01711openalex-snapshot
Palladium-Catalyzed Intramolecular Dearomatization of Indoles via Decarboxylative Alkynyl Termination
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02216openalex-snapshot
Copper-Catalyzed Decarboxylative Atom Transfer Radical Addition of Iododifluoroacetate to Alkynyl Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02919openalex-snapshot
Synthesis of Difluorinated Enynes through Sonogashira-Type Coupling
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00860openalex-snapshot
Selective Synthesis of (E)- and (Z)-Allyl Nitriles via Decarboxylative Reactions of Alkynyl Carboxylic Acids with Azobis(alkylcarbonitriles)
inferred← citeshttps://doi.org/10.1021/acsami.8b08964openalex-snapshot
Novel Covalent Triazine Framework for High-Performance CO2 Capture and Alkyne Carboxylation Reaction
inferred← citeshttps://doi.org/10.1021/acscatal.6b02074openalex-snapshot
Silver-Catalyzed Radical Transformation of Aliphatic Carboxylic Acids to Oxime Ethers
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b02170openalex-snapshot
Sustainable Approach to Waste-Minimized Sonogashira Cross-Coupling Reaction Based on Recoverable/Reusable Heterogeneous Catalytic/Base System and Acetonitrile Azeotrope
inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b05772openalex-snapshot
Ligand Free Heterogeneous Sonogashira Cross-Coupling Reaction over an in Situ Organoiodine Capsulized Palladium Anchored to a Perovskite Catalyst
inferred← citeshttps://doi.org/10.1021/cs300448vopenalex-snapshot
Catalytic C–H Carboxylation of Terminal Alkynes with Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/ja105245fopenalex-snapshot
Room Temperature Palladium-Catalyzed Decarboxylative ortho-Acylation of Acetanilides with α-Oxocarboxylic Acids
inferred← citeshttps://doi.org/10.1021/ja107103bopenalex-snapshot
Palladium-Catalyzed Decarboxylative Couplings of 2-(2-Azaaryl)acetates with Aryl Halides and Triflates
inferred← citeshttps://doi.org/10.1021/ja503295xopenalex-snapshot
Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation
inferred← citeshttps://doi.org/10.1021/ja907448topenalex-snapshot
Theoretical Analysis of Factors Controlling Pd-Catalyzed Decarboxylative Coupling of Carboxylic Acids with Olefins
inferred← citeshttps://doi.org/10.1021/jo1010284openalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Benzyl Halides or Aryl Halides
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/jo1024927openalex-snapshot
Tandem Catalysis: From Alkynoic Acids and Aryl Iodides to 1,2,3-Triazoles in One Pot
inferred← citeshttps://doi.org/10.1021/jo200096xopenalex-snapshot
Pd-Catalyzed Decarboxylative Coupling of Propiolic Acids: One-Pot Synthesis of 1,4-Disubstituted 1,3-Diynes via Sonogashira−Homocoupling Sequence
inferred← citeshttps://doi.org/10.1021/jo300562jopenalex-snapshot
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
inferred← citeshttps://doi.org/10.1021/jo400574dopenalex-snapshot
Palladacycle-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Chlorides under Air
inferred← citeshttps://doi.org/10.1021/jo400716eopenalex-snapshot
Palladium-Catalyzed Decarboxylative Arylation of Benzoylacrylic Acids toward the Synthesis of Chalcones
inferred← citeshttps://doi.org/10.1021/jo4014657openalex-snapshot
Palladacycle-Catalyzed Deacetonative Sonogashira Coupling of Aryl Propargyl Alcohols with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/jo501089kopenalex-snapshot
Copper-Catalyzed Direct Synthesis of Diaryl 1,2-Diketones from Aryl Iodides and Propiolic Acids
inferred← citeshttps://doi.org/10.1021/jo501837popenalex-snapshot
Computational Characterization of the Mechanism for Coinage-Metal-Catalyzed Carboxylation of Terminal Alkynes
inferred← citeshttps://doi.org/10.1021/jo901377bopenalex-snapshot
Catalytic Decarboxylation of 2-Alkynoic Acids
inferred← citeshttps://doi.org/10.1021/jo9022793openalex-snapshot
Palladium-Catalyzed Decarboxylative Cross-Coupling Reaction Between Heteroaromatic Carboxylic Acids and Aryl Halides
inferred← citeshttps://doi.org/10.1021/jp910498yopenalex-snapshot
A Theoretical Study on C−COOH Homolytic Bond Dissociation Enthalpies
inferred← citeshttps://doi.org/10.1021/ol100008qopenalex-snapshot
Pd-Catalyzed Decarboxylative Cross Coupling of Potassium Polyfluorobenzoates with Aryl Bromides, Chlorides, and Triflates
inferred← citeshttps://doi.org/10.1021/ol1004615openalex-snapshot
Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling
inferred← citeshttps://doi.org/10.1021/ol1012857openalex-snapshot
Decarboxylative Acylation of Arenes with α-Oxocarboxylic Acids via Palladium-Catalyzed C−H Activation
inferred← citeshttps://doi.org/10.1021/ol101729kopenalex-snapshot
Synthesis of Vinyl Sulfides by Copper-Catalyzed Decarboxylative C−S Cross-Coupling
inferred← citeshttps://doi.org/10.1021/ol102993yopenalex-snapshot
Pd-Catalyzed Carbonylative Reactions of Aryl Iodides and Alkynyl Carboxylic Acids via Decarboxylative Couplings
inferred← citeshttps://doi.org/10.1021/ol200459vopenalex-snapshot
Pd(II)-Catalyzed Decarboxylative Cross-Coupling of Potassium Aryltrifluoroborates with α-Oxocarboxylic Acids at Room Temperature
inferred← citeshttps://doi.org/10.1021/ol301801ropenalex-snapshot
Decarboxylative Acylation of Cyclic Enamides with α-Oxocarboxylic Acids by Palladium-Catalyzed C–H Activation at Room Temperature
inferred← citeshttps://doi.org/10.1021/ol4004349openalex-snapshot
Pd-Catalyzed Selective Carbonylative and Non-carbonylative Couplings of Propiolic Acid: One-Pot Synthesis of Diarylalkynones
inferred← citeshttps://doi.org/10.1021/ol401358topenalex-snapshot
Metal-Free Decarboxylative Three-Component Coupling Reaction for the Synthesis of Propargylamines
inferred← citeshttps://doi.org/10.1021/ol4037242openalex-snapshot
Copper-Mediated Oxidative Decarboxylative Coupling of Arylpropiolic Acids with Dialkyl H-Phosphonates in Water
inferred← citeshttps://doi.org/10.1039/c002052dopenalex-snapshot
Palladium-catalyzed decarboxylative 1,2-addition of carboxylic acids to aldehydes or imines
inferred← citeshttps://doi.org/10.1039/c0cc00403kopenalex-snapshot
Palladium-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with arylboronic acids
inferred← citeshttps://doi.org/10.1039/c0cc01029dopenalex-snapshot
Pd-catalyzed cross-coupling of carboxylic acids with nitroethane via combination of decarboxylation and dehydrogenation
inferred← citeshttps://doi.org/10.1039/c0cc03772aopenalex-snapshot
Copper-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with aryl halides
inferred← citeshttps://doi.org/10.1039/c0cc04104aopenalex-snapshot
Pd-catalysed decarboxylative Suzuki reactions and orthogonal Cu-based O-arylation of aromatic carboxylic acids
inferred← citeshttps://doi.org/10.1039/c0dt00491jopenalex-snapshot
A DFT study on the Pd-mediated decarboxylation process of aryl carboxylic acids
inferred← citeshttps://doi.org/10.1039/c0dt01234copenalex-snapshot
Pd-catalyzed decarboxylative arylation of silyl enol ester sp3β-C–H bond under aerobic conditions
inferred← citeshttps://doi.org/10.1039/c1cc11635eopenalex-snapshot
Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions
inferred← citeshttps://doi.org/10.1039/c1cs15071eopenalex-snapshot
Recent advances in Sonogashira reactions
inferred← citeshttps://doi.org/10.1039/c1cs15093fopenalex-snapshot
Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
inferred← citeshttps://doi.org/10.1039/c1dt10771bopenalex-snapshot
Mechanism of silver- and copper-catalyzed decarboxylation reactions of aryl carboxylic acids
inferred← citeshttps://doi.org/10.1039/c1ob05969fopenalex-snapshot
Highly effective copper-catalyzed decarboxylative coupling of aryl halides with alkynyl carboxylic acids
inferred← citeshttps://doi.org/10.1039/c1ob06210gopenalex-snapshot
Copper(i)-catalyzed synthesis of 1,3-enynes via coupling between vinyl halides and alkynes or domino coupling of vinyl halides
inferred← citeshttps://doi.org/10.1039/c2ob25643fopenalex-snapshot
Pd-Catalyzed C-3 functionalization of indolizines via C–H bond cleavage
inferred← citeshttps://doi.org/10.1039/c2ra21577bopenalex-snapshot
Copper-catalyzed synthesis of internal alkynesvia domino coupling between 1,1-dihalo-1-alkenes and arylboronic acids
inferred← citeshttps://doi.org/10.1039/c3cc40389kopenalex-snapshot
Copper-promoted decarboxylative direct C3-acylation of N-substituted indoles with α-oxocarboxylic acids
inferred← citeshttps://doi.org/10.1039/c3ob40748aopenalex-snapshot
Bu4NI-catalyzed decarboxylative acyloxylation of an sp3 C–H bond adjacent to a heteroatom with α-oxocarboxylic acids
inferred← citeshttps://doi.org/10.1039/c3ra41442fopenalex-snapshot
Transition metal-catalyzed decarboxylative coupling reactions of alkynyl carboxylic acids
inferred← citeshttps://doi.org/10.1039/c3ra43144dopenalex-snapshot
Cu/Ag-catalyzed double decarboxylative cross-coupling reaction between cinnamic acids and aliphatic acids in aqueous solution
inferred← citeshttps://doi.org/10.1039/c3ra47712fopenalex-snapshot
Synthesis of diarylalkynes via tandem Sonogashira/decarboxylative reaction of aryl chlorides with propiolic acid
inferred← citeshttps://doi.org/10.1039/c4ra12782jopenalex-snapshot
A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one
inferred← citeshttps://doi.org/10.1039/c5dt03794hopenalex-snapshot
1,1′-Bis(di-tert-butylphosphino)ferrocene copper( i ) complex catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c5nj02630jopenalex-snapshot
Metal–organic framework MIL-101 supported bimetallic Pd–Cu nanocrystals as efficient catalysts for chromium reduction and conversion of carbon dioxide at room temperature
inferred← citeshttps://doi.org/10.1039/c5ra06168gopenalex-snapshot
Pd-catalyzed decarboxylative allylic coupling of acetates of Baylis–Hillman alcohols with propiolic acids: a highly regio- and stereoselective synthesis of 1,5-diarylpent-1-en-4-yne derivatives
inferred← citeshttps://doi.org/10.1039/c6ra12046fopenalex-snapshot
Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesis
inferred← citeshttps://doi.org/10.1039/c6ra12916aopenalex-snapshot
Decarboxylative/Sonogashira-type cross-coupling using PdCl 2 (Cy*Phine) 2
inferred← citeshttps://doi.org/10.1039/c6ra23742hopenalex-snapshot
Functionalized α,β-ynones: efficient ligand for Cu catalyzed Sonogashira-type cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/c7cy01126aopenalex-snapshot
Polystyrene supported palladium nanoparticles catalyzed cinnamic acid synthesis using maleic anhydride as a substitute for acrylic acid
inferred← citeshttps://doi.org/10.1039/c7gc00923bopenalex-snapshot
A Schiff base-modified silver catalyst for efficient fixation of CO 2 as carboxylic acid at ambient pressure
inferred← citeshttps://doi.org/10.1039/c7gc02949gopenalex-snapshot
Decarboxylative reactions with and without light – a comparison
inferred← citeshttps://doi.org/10.1039/c7nj00877eopenalex-snapshot
Pd(NHC)PEPPSI-diazonium salts: an efficient blend for the decarboxylative Sonogashira cross coupling reaction
inferred← citeshttps://doi.org/10.1039/c7nj03038jopenalex-snapshot
cis -1,2-Bis(diphenylphosphino)ethylene copper( i ) catalyzed C–H activation and carboxylation of terminal alkynes
inferred← citeshttps://doi.org/10.1039/c7ob01334eopenalex-snapshot
Calcium carbide catalytically activated with tetra-n-butyl ammonium fluoride for Sonogashira cross coupling reactions
inferred← citeshttps://doi.org/10.1039/c7ra02758copenalex-snapshot
Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst
inferred← citeshttps://doi.org/10.1039/c7ra07324kopenalex-snapshot
Alternating magnetic field mediated micro reaction system for palladium-catalyzed coupling reactions
inferred← citeshttps://doi.org/10.1039/c8gc01180jopenalex-snapshot
Visible-light induced copper( i )-catalysed denitrogenative oxidative coupling of hydrazinylpyridines with terminal alkynes
inferred← citeshttps://doi.org/10.1039/c8nj02286kopenalex-snapshot
Flower-like AgNPs@m-MgO as an excellent catalyst for CO 2 fixation and acylation reactions under ambient conditions
inferred← citeshttps://doi.org/10.1039/c8nj02964dopenalex-snapshot
Pd-Catalyzed decarboxylative alkynylation of alkynyl carboxylic acids with arylsulfonyl hydrazides via a desulfinative process
inferred← citeshttps://doi.org/10.1039/c9cs00571dopenalex-snapshot
Metal-catalysed C–Het (F, O, S, N) and C–C bond arylation
inferred← citeshttps://doi.org/10.1039/d0qo01133aopenalex-snapshot
Palladium-catalyzed decarboxylative gem -selective addition of alkynoic acids to terminal alkynes
inferred← citeshttps://doi.org/10.1039/d1ob01435hopenalex-snapshot
Vinyl sulfone synthesis via copper-catalyzed three-component decarboxylative addition
inferred← citeshttps://doi.org/10.1039/d3cy01765fopenalex-snapshot
Supported Pd-catalyzed decarboxylative carbonylation reaction of 2-alkynoic acids and aryl iodides
inferred← citeshttps://doi.org/10.1039/d3na00096fopenalex-snapshot
One-pot synthesis of gamma-graphyne supported Pd nanoparticles with high catalytic activity
inferred← citeshttps://doi.org/10.1039/d3qo01122dopenalex-snapshot
Iron-photocatalyzed double decarboxylative coupling reactions of alkynoic acids and alkyl carboxylic acids: access to alkylated alkynes
inferred← citeshttps://doi.org/10.1039/d5qo00339copenalex-snapshot
Palladium-catalyzed chemoselective decarboxylative coupling of alkynyl carboxylic acids with halogenated aryl triflates
inferred← citeshttps://doi.org/10.1039/d5qo00601eopenalex-snapshot
A general protocol for efficient construction of perfluoro- tert -butyl alkynes with (perfluoro- tert -butyl)propiolic acid
inferred← citeshttps://doi.org/10.1039/d6cc01731bopenalex-snapshot
Preactivation-free direct decarboxylative alkynylation of indoleacetic acids: access to alkynyl-functionalized indoles
inferred← citeshttps://doi.org/10.1039/d6nj01211fopenalex-snapshot
Transition metal complexes of trans -1,2-bis(diphenylphosphino)ethylene: structural insights and carboxylation of terminal alkynes with carbon dioxide
inferred← citeshttps://doi.org/10.1039/d6ra01629dopenalex-snapshot
An account on using bio-renewable solvents in organic synthesis: advances, prospects, and challenges
inferred← citeshttps://doi.org/10.1055/a-1750-3080openalex-snapshot
Dehydrative and Decarboxylative Coupling of Alkynoic Acids with Allylic Alcohols
inferred← citeshttps://doi.org/10.1246/bcsj.20100327openalex-snapshot
2,2′-Diamino-6,6′-dimethylbiphenyl as an Efficient Ligand in the CuI-Catalyzed Sonogashira Reaction of Aryl Iodides and Bromides with Terminal Alkynes
inferred← citeshttps://doi.org/10.1246/cl.180610openalex-snapshot
The Gold-catalyzed Formal Hydration, Decarboxylation, and [4+2] Cycloaddition of Alkyne Derivatives Featuring L2/Z-type Diphosphinoborane Ligands
inferred← citeshttps://doi.org/10.2174/2211544711666220210125547openalex-snapshot
Progress in Catalytic Decarboxylative Oxidative C-H Alkynylation
inferred← citeshttps://doi.org/10.3389/fchem.2021.773855openalex-snapshot
An Efficient and Sustainable Approach to Decarboxylative Cross-Coupling Using Silica Coated Magnetic Copper Nanocatalyst for the Synthesis of Internal Alkynes
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.10.36openalex-snapshot
Practical synthesis of aryl-2-methyl-3-butyn-2-ols from aryl bromides via conventional and decarboxylative copper-free Sonogashira coupling reactions
inferred← citeshttps://doi.org/10.3998/ark.5550190.p009.632openalex-snapshot
Mechanistic studies on the metal-free decarboxylative coupling reaction for synthesis of propargylamines by NMR
inferred← citeshttps://doi.org/10.5012/bkcs.2013.34.7.2099openalex-snapshot
Ligand Effect in Recycled CNT-Pd Heterogeneous Catalyst for Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.78.619openalex-snapshot
Synthesis of Gold Catalyst Featuring Z-Type Ligand and Its Catalyic Reaction
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