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One-Pot Synthesis of Diarylalkynes Using Palladium-Catalyzed Sonogashira Reaction and Decarboxylative Coupling of sp Carbon and sp2 Carbon
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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.200505095openalex-snapshot
A Convenient High Activity Catalyst for the Sonogashira Coupling of Aryl Bromides
inferredcites →https://doi.org/10.1002/anie.200353015openalex-snapshot
Efficient Palladium‐Catalyzed Coupling of Aryl Chlorides and Tosylates with Terminal Alkynes: Use of a Copper Cocatalyst Inhibits the Reaction
inferredcites →https://doi.org/10.1002/anie.200600721openalex-snapshot
A Versatile Hexadiene Synthesis by Decarboxylative sp3–sp3 Coupling/Cope Rearrangement
inferredcites →https://doi.org/10.1002/anie.200602761openalex-snapshot
Palladium‐Based Catalytic Systems for the Synthesis of Conjugated Enynes by Sonogashira Reactions and Related Alkynylations
inferredcites →https://doi.org/10.1016/j.tetlet.2005.01.044openalex-snapshot
Sonogashira cross-coupling reactions with heteroaryl halides in the presence of a tetraphosphine–palladium catalyst
inferredcites →https://doi.org/10.1021/jo026877topenalex-snapshot
Pd Nanoparticles Catalyzed Stereospecific Synthesis of β-Aryl Cinnamic Esters in Ionic Liquids
inferredcites →https://doi.org/10.1021/jo052423vopenalex-snapshot
Solvent and Base Dependence of Copper-Free Palladium-Catalyzed Cross-Couplings between Terminal Alkynes and Arylic Iodides: Development of Efficient Conditions for the Construction of Gold(III)/Free-Base Porphyrin Dimers
inferredcites →https://doi.org/10.5860/choice.43-0331openalex-snapshot
Metal-catalyzed cross-coupling reactions
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
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11451.pub2openalex-snapshot
Tris(dibenzylideneacetone)dipalladium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11451.pub3openalex-snapshot
Tris(dibenzylideneacetone)dipalladium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11451.pub4openalex-snapshot
Tris(dibenzylideneacetone)dipalladium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11451.pub5openalex-snapshot
Tris(dibenzylideneacetone)dipalladium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11451.pub6openalex-snapshot
Tris(dibenzylideneacetone)dipalladium
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Alkylation, Alkenylation, and Arylation of Alkynes and Allenes
inferred← citeshttps://doi.org/10.1002/9783527680092.ch4openalex-snapshot
Reactions Involving Elimination of CO 2 and Ketones
inferred← citeshttps://doi.org/10.1002/adsc.200900337openalex-snapshot
Synthesis of Biaryls and Aryl Ketones via Microwave‐Assisted Decarboxylative Cross‐Couplings
inferred← citeshttps://doi.org/10.1002/adsc.200900502openalex-snapshot
Palladium‐Catalyzed Decarboxylative sp‐sp2 Cross‐Coupling Reactions of Aryl and Vinyl Halides and Triflates with α,β‐Ynoic Acids using Silver Oxide
inferred← citeshttps://doi.org/10.1002/adsc.200900886openalex-snapshot
Sulfonated N‐Heterocyclic Carbenes for Pd‐Catalyzed Sonogashira and Suzuki–Miyaura Coupling in Aqueous Solvents
inferred← citeshttps://doi.org/10.1002/adsc.201000564openalex-snapshot
Synthesis of Propiolic Acids via Copper‐Catalyzed Insertion of Carbon Dioxide into the CH Bond of Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/adsc.201000897openalex-snapshot
Synthesis of 1,4‐Diarylbuta‐1,3‐dienes through Palladium‐ Catalyzed Decarboxylative Coupling of Unsaturated Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/adsc.201100238openalex-snapshot
Synthesis of Diarylalkynes by Iron/Copper Co‐Catalyzed Decarboxylative spsp2 Coupling of Alkynyl Carboxylic Acids and Aryl Halides
inferred← citeshttps://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
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.201200383openalex-snapshot
β‐Aryl Nitrile Construction via Palladium‐Catalyzed Decarboxylative Benzylation of α‐Cyano Aliphatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/adsc.201200876openalex-snapshot
Phosphine‐Free Palladium‐Catalyzed Decarboxylative Coupling of Alkynylcarboxylic Acids with Aryl and Heteroaryl Halides
inferred← citeshttps://doi.org/10.1002/adsc.201201106openalex-snapshot
Palladium‐Catalyzed Synthesis of (Z)‐3‐Arylthioacrylic Acids and Thiochromenones
inferred← citeshttps://doi.org/10.1002/adsc.201300078openalex-snapshot
Palladium‐Catalyzed Decarboxylative Coupling of α‐ Oxocarboxylic Acids with C(sp2)H of 2‐Aryloxypyridines
inferred← citeshttps://doi.org/10.1002/adsc.201300945openalex-snapshot
Chemoselective Synthesis of Unsymmetrical Internal Alkynes or Vinyl Sulfones via Palladium‐Catalyzed Cross‐Coupling Reaction of Sodium Sulfinates with Alkynes
inferred← citeshttps://doi.org/10.1002/adsc.201500686openalex-snapshot
Palladium‐Catalyzed Domino Process: Synthesis of Symmetrical Diarylalkynes, cis‐ and trans‐Alkenes using Lithium Acetylide as a Synthon
inferred← citeshttps://doi.org/10.1002/adsc.201500803openalex-snapshot
Regioselective Copper‐Catalyzed Oxidative Cross‐Coupling of Imidazo[1,2‐ a ]pyridines with Methyl Ketones: An Efficient Route for Synthesis of 1,2‐Diketones
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Rhodium(III)‐Catalyzed Regioselective Decarboxylative Cyclization for the Synthesis of 4 H ‐Furo[3,2‐ c ]chromen‐4‐one Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201701128openalex-snapshot
One‐Pot Domino Synthesis of Diarylalkynes/1,4‐Diaryl‐1,3‐diynes by [9,9‐Dimethyl‐4,5‐bis(diphenylphosphino)xanthene] (Xantphos)–Copper(I) Iodide–Palladium(II) Acetate‐Catalyzed Double Sonogashira‐Type Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201701406openalex-snapshot
Cobalt(III)−Catalyzed C−H Activation: A Secondary Amide Directed Decarboxylative Functionalization of Alkynyl Carboxylic Acids Wherein Amide NH‐group Remains Unreactive
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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
inferred← citeshttps://doi.org/10.1002/ajoc.201600109openalex-snapshot
Copper‐Catalyzed Double Decarboxylative Coupling Reactions of Alkynyl Carboxylic Acid and Glyoxylic Acid: Synthesis of Propargyl Amines and Imidazopyridines
inferred← citeshttps://doi.org/10.1002/ajoc.201600524openalex-snapshot
Highly Selective Synergistic Copper(I/II)‐Catalyzed A3 Cross Coupling/Decarboxylative A3 Domino Reactions in Water
inferred← citeshttps://doi.org/10.1002/ajoc.202000449openalex-snapshot
Sequential One‐Pot Coupling Reactions of Diiodobenzenes, Propiolic Acid, and Aryl Halides for the Synthesis of Diarylalkynyl Arenes
inferred← citeshttps://doi.org/10.1002/ajoc.202100454openalex-snapshot
Metal‐Free Doubly Decarboxylative Three‐Component Reaction: Synthesis of Propargyl Amines
inferred← citeshttps://doi.org/10.1002/ajoc.202100650openalex-snapshot
Benzils: A Review on their Synthesis
inferred← citeshttps://doi.org/10.1002/ange.200904916openalex-snapshot
Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
inferred← citeshttps://doi.org/10.1002/ange.200905953openalex-snapshot
Decarboxylative Cross‐Coupling of Aryl Tosylates with Aromatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/ange.201100378openalex-snapshot
A Colorimetric High‐Throughput Screening Method for Palladium‐Catalyzed Coupling Reactions of Aryl Iodides Using a Gold Nanoparticle‐Based Iodide‐Selective Probe
inferred← citeshttps://doi.org/10.1002/ange.201100765openalex-snapshot
Migratory Decarboxylative Coupling of Coumarins: Synthetic and Mechanistic Aspects
inferred← citeshttps://doi.org/10.1002/ange.201208025openalex-snapshot
Decarboxylierende Kreuzkupplung von Mesylaten katalysiert durch ein Kupfer/Palladium‐System mit maßgeschneiderten Imidazolylphosphanliganden
inferred← citeshttps://doi.org/10.1002/ange.201409103openalex-snapshot
An Efficient Nanoscale Heterogeneous Catalyst for the Capture and Conversion of Carbon Dioxide at Ambient Pressure
inferred← citeshttps://doi.org/10.1002/ange.201504559openalex-snapshot
Decarboxylative Alkynylation and Carbonylative Alkynylation of Carboxylic Acids Enabled by Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ange.201505843openalex-snapshot
Katalytische decarboxylierende Kreuzkupplung von Arylchloriden mit Benzoaten ohne aktivierende ortho‐Substituenten
inferred← citeshttps://doi.org/10.1002/anie.200904916openalex-snapshot
Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
inferred← citeshttps://doi.org/10.1002/anie.200905953openalex-snapshot
Decarboxylative Cross‐Coupling of Aryl Tosylates with Aromatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/anie.201100378openalex-snapshot
A Colorimetric High‐Throughput Screening Method for Palladium‐Catalyzed Coupling Reactions of Aryl Iodides Using a Gold Nanoparticle‐Based Iodide‐Selective Probe
inferred← citeshttps://doi.org/10.1002/anie.201100765openalex-snapshot
Migratory Decarboxylative Coupling of Coumarins: Synthetic and Mechanistic Aspects
inferred← citeshttps://doi.org/10.1002/anie.201208025openalex-snapshot
Decarboxylative Cross‐Coupling of Mesylates Catalyzed by Copper/Palladium Systems with Customized Imidazolyl Phosphine Ligands
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
inferred← citeshttps://doi.org/10.1002/anie.201504559openalex-snapshot
Decarboxylative Alkynylation and Carbonylative Alkynylation of Carboxylic Acids Enabled by Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201505843openalex-snapshot
Catalytic Decarboxylative Cross‐Coupling of Aryl Chlorides and Benzoates without Activating ortho Substituents
inferred← citeshttps://doi.org/10.1002/aoc.2921openalex-snapshot
Mechanistic study of palladium‐catalyzed decarboxylative coupling of phenylpropiolic acid and aryl iodide
inferred← citeshttps://doi.org/10.1002/aoc.4914openalex-snapshot
Palladium‐catalyzed decarboxylative coupling of α,β‐unsaturated carboxylic acids with aryl tosylates
inferred← citeshttps://doi.org/10.1002/aoc.6328openalex-snapshot
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.11298openalex-snapshot
Aryl Chlorides as Coupling Partners in the Palladium‐catalyzed Decarboxylative Coupling Reactions of Propiolic Acids
inferred← citeshttps://doi.org/10.1002/bkcs.12221openalex-snapshot
Palladium‐Catalyzed Decarboxylative Homodimerization of Propiolic Acids: Synthesis of 1, 3‐Enynes
inferred← citeshttps://doi.org/10.1002/cctc.200900277openalex-snapshot
Comparative Study of Copper‐ and Silver‐Catalyzed Protodecarboxylations of Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/cctc.201200047openalex-snapshot
CH Carboxylation of Terminal Alkynes Catalyzed by Low Loadings of Silver(I)/DMSO at Ambient CO2 Pressure
inferred← citeshttps://doi.org/10.1002/cctc.202300601openalex-snapshot
Recent Advances in Nickel‐Catalyzed Synthesis of Allenes: New Insights and Perspectives
inferred← citeshttps://doi.org/10.1002/cctc.202401821openalex-snapshot
Decarboxylative Cross‐Dehydrogenative Coupling of Tetrahydroisoquinoline and Alkynoic Acids Using Recyclable Carbon Nanotube Supported Copper/Nickel Oxide Catalysts
inferred← citeshttps://doi.org/10.1002/chem.200900133openalex-snapshot
Synthesis of Aryl Sulfides by Decarboxylative CS Cross‐Couplings
inferred← citeshttps://doi.org/10.1002/chem.200903319openalex-snapshot
Low‐Temperature Ag/Pd‐Catalyzed Decarboxylative Cross‐Coupling of Aryl Triflates with Aromatic Carboxylate Salts
inferred← citeshttps://doi.org/10.1002/chem.201000529openalex-snapshot
A Versatile Catalyst for Intermolecular Direct Arylation of Indoles with Benzoic Acids as Arylating Reagents
inferred← citeshttps://doi.org/10.1002/chem.201200829openalex-snapshot
Pd‐Catalyzed Cross‐Coupling of Aryl Carboxylic Acids with Propiophenones through a Combination of Decarboxylation and Dehydrogenation
inferred← citeshttps://doi.org/10.1002/chem.201301818openalex-snapshot
A Highly Efficient Palladium‐Catalyzed Decarboxylative ortho‐Acylation of Azobenzenes with α‐Oxocarboxylic Acids: Direct Access to Acylated Azo Compounds
inferred← citeshttps://doi.org/10.1002/chem.201402931openalex-snapshot
The ortho‐Substituent Effect on the Ag‐Catalysed Decarboxylation of Benzoic Acids
inferred← citeshttps://doi.org/10.1002/chem.201405715openalex-snapshot
Ru‐Catalyzed Decarboxylative Annulations of α‐Keto Acids with Internal Alkynes: Dual Roles of COOH as Directing Group and Leaving Group
inferred← citeshttps://doi.org/10.1002/chem.201405716openalex-snapshot
The Gold(I)‐Catalysed Protodecarboxylation Mechanism
inferred← citeshttps://doi.org/10.1002/chin.200832095openalex-snapshot
ChemInform Abstract: One‐Pot Synthesis of Diarylalkynes Using Palladium‐Catalyzed Sonogashira Reaction and Decarboxylative Coupling of sp Carbon and sp2 Carbon.
inferred← citeshttps://doi.org/10.1002/ejoc.201100659openalex-snapshot
Phosphane‐Free Copper‐Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Halides under Aerobic Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201101770openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/ejoc.201301441openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/ejoc.201700110openalex-snapshot
Three‐Component One‐Pot Synthesis of Unsymmetrical Diarylalkynes by Thermocontrolled Sequential Sonogashira Reactions Using Potassium Ethynyltrifluoroborate
inferred← citeshttps://doi.org/10.1002/ejoc.201900270openalex-snapshot
Cobalt(III)‐Catalyzed Direct ortho‐Alkenylation of Arylpyrazoles: A Comparative Study on Decarboxylation and Desilylation
inferred← citeshttps://doi.org/10.1002/ejoc.201900982openalex-snapshot
Retracted: Copper‐Catalyzed Decarboxylative C(sp 2 )‐C(sp 3 ) and C(sp)‐C(sp 3 ) Coupling of Substituted Cinnamic Acids and 3‐Phenyl Propiolic Acid with N‐Tosyl Oxaziridines
inferred← citeshttps://doi.org/10.1002/ejoc.202100275openalex-snapshot
Copper‐Free One‐Pot Sonogashira‐Type Coupling for the Efficient Preparation of Symmetric Diarylalkyne Ligands for Metal‐Organic Cages**
inferred← citeshttps://doi.org/10.1002/ijch.201000039openalex-snapshot
Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.1002/slct.201800758openalex-snapshot
Cu I /Ag I ‐Promoted Decarboxylative Alkynylation of ortho‐Nitro Benzoic Acids
inferred← citeshttps://doi.org/10.1002/slct.201803669openalex-snapshot
Nanoporous ZnO Supported CuBr (CuBr/ZnO): An Efficient Catalyst for CO 2 Fixation Reactions
inferred← citeshttps://doi.org/10.1002/slct.201803805openalex-snapshot
Synthesis of Di‐Substituted Alkynes via Palladium‐Catalyzed Decarboxylative Coupling and C‐H Activation
inferred← citeshttps://doi.org/10.1002/slct.202102494openalex-snapshot
Copper‐Catalyzed Decarboxylative Cycloaddition of Alkynyl Carboxylic Acids and Sodium Azide with Epoxides and Ethers
inferred← citeshttps://doi.org/10.1002/slct.202203186openalex-snapshot
Graphene‐based Composite Materials as Catalyst for Organic Transformations
inferred← citeshttps://doi.org/10.1007/3418_2012_44openalex-snapshot
Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_1openalex-snapshot
Transition Metal-Catalyzed Decarboxylation and Decarboxylative Cross-Couplings
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_2openalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Potassium Oxalate Monoester with Aryl and Alkenyl Halides
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_3openalex-snapshot
Synthesis of Polyfluorobiaryls via Copper-Catalyzed Decarboxylative Couplings of Potassium Polyfluorobenzoates with Aryl Bromides and Iodides
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_4openalex-snapshot
Palladium-Catalyzed Decarboxylative Couplings of Potassium Polyfluorobenzoates with Aryl Bromides, Chlorides, and Triflates
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_5openalex-snapshot
Construction of C(sp3)–C(sp2) Bonds Via Palladium-Catalyzed Decarboxylative Couplings of 2-(2-Azaaryl)Acetate Salts with Aryl Halides
inferred← citeshttps://doi.org/10.1007/978-981-10-3193-9_8openalex-snapshot
Palladium-Catalyzed Decarboxylative Benzylation of α-Cyano Aliphatic Carboxylate Salts with Benzyl Electrophiles
inferred← citeshttps://doi.org/10.1007/978-981-99-8822-8_1openalex-snapshot
CO2 Conversion via MOF-Based Catalysts
inferred← citeshttps://doi.org/10.1007/s11426-011-4381-0openalex-snapshot
Transition metal-catalyzed decarboxylative cross-coupling reactions
inferred← citeshttps://doi.org/10.1007/s13738-023-02805-xopenalex-snapshot
On-water biphasic organic synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-817592-7.00010-1openalex-snapshot
One-pot strategy: A highly economical tool in organic synthesis and medicinal chemistry
inferred← citeshttps://doi.org/10.1016/b978-0-323-89851-5.00011-1openalex-snapshot
Graphene-based nanomaterials for CO2 capture and conversion
inferred← citeshttps://doi.org/10.1016/j.catcom.2013.12.029openalex-snapshot
Palladium nanoparticles catalyzed Sonogashira reactions for the one-pot synthesis of symmetrical and unsymmetrical diarylacetylenes
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.05.025openalex-snapshot
Zeolite-based copper catalyst for decarboxylative coupling of alkynyl carboxylic acids with aryl iodides
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.10.018openalex-snapshot
Base free palladium-Ag2O catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with triarylbismuth reagents
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.04.019openalex-snapshot
Nickel-catalyzed cross-coupling reaction of alkynyl bromides with Grignard reagents
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.02.001openalex-snapshot
Metal-organic framework-based heterogeneous catalysts for the conversion of C1 chemistry: CO, CO2 and CH4
inferred← citeshttps://doi.org/10.1016/j.ccr.2023.215138openalex-snapshot
Catalytic C(sp)-H carboxylation with CO2
inferred← citeshttps://doi.org/10.1016/j.inoche.2012.05.013openalex-snapshot
Synthesis, characterization of palladium hydroxysalen complex and its application in the coupling reaction of arylboronic acids: Mizoroki–Heck type reaction and decarboxylative couplings
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2012.11.029openalex-snapshot
Ligand-free palladium-catalyzed decarboxylative coupling reactions of aryl iodides and alkynyl carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2019.03.015openalex-snapshot
Domino [Pd]-Catalysis: Heck followed by decarboxylative Sonogashira couplings under microwave irradiation in aqueous medium
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.reactfunctpolym.2023.105643openalex-snapshot
Carbon-supported statistically distributed polyethyleneimine/palladium (II) complexes as efficient and sustainable Sonogashira catalysts
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.2009.03.064openalex-snapshot
The first Cu- and amine-free Sonogashira-type cross-coupling in the C-6-alkynylation of protected 2′-deoxyadenosine
inferred← citeshttps://doi.org/10.1016/j.tet.2011.05.031openalex-snapshot
CuI-catalyzed Suzuki coupling reaction of organoboronic acids with alkynyl bromides
inferred← citeshttps://doi.org/10.1016/j.tet.2011.08.042openalex-snapshot
Calcium carbide as a cost-effective starting material for symmetrical diarylethynes via Pd-catalyzed coupling reaction
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.tet.2016.05.012openalex-snapshot
Cu(I)/Ag(I)-mediated decarboxylative trifluoromethylation of arylpropiolic acids with Me 3 SiCF 3 at room temperature
inferred← citeshttps://doi.org/10.1016/j.tet.2018.08.050openalex-snapshot
Highly efficient synthesis of 1,2-disubstituted acetylenes derivatives from the cross-coupling reactions of 1-bromoalkynes with organoalane reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.030openalex-snapshot
Palladium-catalyzed decarboxylative aminocarbonylation with alkynoic acid and tertiary amine for the synthesis of alkynyl amide
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132370openalex-snapshot
Highly efficient synthesis of 1,2-disubstituted acetylenes derivatives from the cross-coupling reactions of 1-bromoalkynes with organotitanium reagents
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.2011.07.091openalex-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.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.2015.08.075openalex-snapshot
CuI/CuBr2-catalyzed decarboxylative/A3 reaction of propiolic acids for the facile synthesis of 1,4-diheterocycle-2-butynes
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.2016.08.095openalex-snapshot
Palladium-catalyzed decarboxylative coupling reaction with alkynyl carboxylic acids and arylsiloxanes
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/10.1021/acs.jchemed.2c00421openalex-snapshot
Synthesis of Arylpropiolic Acids via Carboxylation of Arylacetylenic Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00669openalex-snapshot
Decarboxylative Oxyacyloxylation of Propiolic Acids: Construction of Alkynyl-Containing α-Acyloxy Ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00762openalex-snapshot
Decarboxylative Addition of Propiolic Acids with Indoles to Synthesize Bis(indolyl)methane Derivatives with a Pd(II)/LA Catalyst
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.joc.6b00883openalex-snapshot
Nickel-Catalyzed Hiyama-type Decarboxylative Coupling of Propiolic Acids and Organosilanes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02175openalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Alkenyl Tosylates for the Synthesis of Enynones
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00998openalex-snapshot
Catalytic Activation of Trimethylsilylacetylenes: A One-Pot Route to Unsymmetrical Acetylenes and Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03285openalex-snapshot
Copper-Catalyzed Decarboxylative Cycloaddition of Propiolic Acids, Azides, and Arylboronic Acids: Construction of Fully Substituted 1,2,3-Triazoles
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00051openalex-snapshot
Pd-Catalyzed Cross-Couplings: On the Importance of the Catalyst Quantity Descriptors, mol % and ppm
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00214openalex-snapshot
A Comparative Study of Dibenzylideneacetone Palladium Complexes in Catalysis
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00298openalex-snapshot
Modular Synthesis of Diarylalkynes and Their Efficient Conversion into Luminescent Tetraarylbutadienes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01269openalex-snapshot
Fast Heck–Cassar–Sonogashira (HCS) Reactions in Green Solvents
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00173openalex-snapshot
Coupling Photocatalysis and Substitution Chemistry to Expand and Normalize Redox-Active Halides
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.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/acs.orglett.7b03325openalex-snapshot
Ruthenium-Catalyzed C–H Activation of Salicylaldehyde and Decarboxylative Coupling of Alkynoic Acids for the Selective Synthesis of Homoisoflavonoids and Flavones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03922openalex-snapshot
Copper-Catalyzed Decarboxylative Disulfonylation of Alkynyl Carboxylic Acids with Sulfinic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00520openalex-snapshot
Copper-Catalyzed Decarboxylative Oxyalkylation of Alkynyl Carboxylic Acids: Synthesis of γ-Diketones and γ-Ketonitriles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01625openalex-snapshot
Ni/Cu-Catalyzed Decarboxylative Addition of Alkynoic Acids to Terminal Alkynes for the Synthesis of gem-1,3-Enynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02907openalex-snapshot
Selective Mono- and Dialkynylation of 1-Fluoro-2,2-diiodovinylarenes Using Pd-Catalyzed Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.5c03724openalex-snapshot
Remote Asymmetric Induction via a Chiral Acetylene Equivalent
inferred← citeshttps://doi.org/10.1021/acscatal.9b04593openalex-snapshot
Arylation of Terminal Alkynes by Aryl Iodides Catalyzed by a Parts-per-Million Loading of Palladium Acetate
inferred← citeshttps://doi.org/10.1021/acsomega.7b01165openalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Tosylates
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b02678openalex-snapshot
Knitting Aryl Network Polymers-Incorporated Ag Nanoparticles: A Mild and Efficient Catalyst for the Fixation of CO2 as Carboxylic Acid
inferred← citeshttps://doi.org/10.1021/ja1035557openalex-snapshot
Decarboxylative Benzylations of Alkynes and Ketones
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/ja900984xopenalex-snapshot
Synthesis of Aromatic Esters via Pd-Catalyzed Decarboxylative Coupling of Potassium Oxalate Monoesters with Aryl Bromides and Chlorides
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/jacs.1c03394openalex-snapshot
Iron-Catalyzed Tandem Cyclization of Diarylacetylene to a Strained 1,4-Dihydropentalene Framework for Narrow-Band-Gap Materials
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/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/jo2007253openalex-snapshot
One-Pot Synthesis of Symmetrical and Unsymmetrical Aryl Sulfides by Pd-Catalyzed Couplings of Aryl Halides and Thioacetates
inferred← citeshttps://doi.org/10.1021/jo201770jopenalex-snapshot
Synthesis of π-Conjugated Molecules Based on 3,4-Dioxypyrroles via Pd-Mediated Decarboxylative Cross-Coupling
inferred← citeshttps://doi.org/10.1021/jo202644gopenalex-snapshot
A Guide to Sonogashira Cross-Coupling Reactions: The Influence of Substituents in Aryl Bromides, Acetylenes, and Phosphines
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/jo400616ropenalex-snapshot
Copper-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylates with 1,1-Dibromo-1-alkenes
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/jo5003032openalex-snapshot
Palladium-Catalyzed Decarboxylative Trifluoroethylation of Aryl Alkynyl Carboxylic Acids
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/jo802290ropenalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Aryl Halides
inferred← citeshttps://doi.org/10.1021/jo901377bopenalex-snapshot
Catalytic Decarboxylation of 2-Alkynoic Acids
inferred← citeshttps://doi.org/10.1021/jo902319hopenalex-snapshot
Aldehyde- and Ketone-Induced Tandem Decarboxylation-Coupling (Csp3−Csp) of Natural α-Amino Acids and Alkynes
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/ol100231gopenalex-snapshot
3,4-Propylenedioxypyrrole-Based Conjugated Oligomers via Pd-Mediated Decarboxylative Cross Coupling
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/ol200638zopenalex-snapshot
Ligand-Free Ag(I)-Catalyzed Carboxylation of Terminal Alkynes with CO2
inferred← citeshttps://doi.org/10.1021/ol201750sopenalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Potassium Nitrophenyl Acetates with Aryl Halides
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