On the public citation graph

Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling

https://doi.org/10.1021/ol1004615
0 signed · 318 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980302)37:4<489::aid-anie489>3.0.co;2-nopenalex-snapshot
N-Functionalized 1-Alkynylamides: New Building Blocks for Transition Metal Mediated Inter- and Intramolecular [2+2+1] Cycloadditions
inferredcites →https://doi.org/10.1002/1521-3773(20000804)39:15<2632::aid-anie2632>3.0.co;2-fopenalex-snapshot
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/anie.200300594openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200300630openalex-snapshot
Palladium Oxidase Catalysis: Selective Oxidation of Organic Chemicals by Direct Dioxygen‐Coupled Turnover
inferredcites →https://doi.org/10.1002/anie.200390221openalex-snapshot
From Alkenylsilanes to Ketones with Air as the Oxidant
inferredcites →https://doi.org/10.1002/anie.200490023openalex-snapshot
Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
inferredcites →https://doi.org/10.1002/anie.200601889openalex-snapshot
Enantioselective Palladium‐Catalyzed Decarboxylative Allylic Alkylations
inferredcites →https://doi.org/10.1002/anie.200602270openalex-snapshot
Diastereoselective Gold‐Catalyzed Cycloisomerizations of Ene‐Ynamides
inferredcites →https://doi.org/10.1002/anie.200604494openalex-snapshot
New Approaches for Decarboxylative Biaryl Coupling
inferredcites →https://doi.org/10.1002/anie.200704782openalex-snapshot
Carboxylic Acids as Substrates in Homogeneous Catalysis
inferredcites →https://doi.org/10.1002/anie.200705127openalex-snapshot
Synthesis of Ketones from α‐Oxocarboxylates and Aryl Bromides by Cu/Pd‐Catalyzed Decarboxylative Cross‐Coupling
inferredcites →https://doi.org/10.1002/anie.200800602openalex-snapshot
Visible‐Light‐Driven Oxidation of Organic Contaminants in Air with Gold Nanoparticle Catalysts on Oxide Supports
inferredcites →https://doi.org/10.1002/anie.200800728openalex-snapshot
Palladium/Copper‐Catalyzed Decarboxylative Cross‐Coupling of Aryl Chlorides with Potassium Carboxylates
inferredcites →https://doi.org/10.1002/anie.200805122openalex-snapshot
The Copper‐Catalyzed Decarboxylative Coupling of the sp3‐Hybridized Carbon Atoms of α‐Amino Acids
inferredcites →https://doi.org/10.1002/anie.200901099openalex-snapshot
Copper‐Mediated Coupling of 1,1‐Dibromo‐1‐alkenes with Nitrogen Nucleophiles: A General Method for the Synthesis of Ynamides
inferredcites →https://doi.org/10.1002/anie.200904916openalex-snapshot
Copper‐Catalyzed Decarboxylative Cross‐Coupling of Potassium Polyfluorobenzoates with Aryl Iodides and Bromides
inferredcites →https://doi.org/10.1002/chem.200802301openalex-snapshot
Synthesis of Tricyclic Fused 3‐Aminopyridines through Intramolecular CoI‐Catalyzed [2+2+2] Cycloaddition between Ynamides, Nitriles, and Alkynes
inferredcites →https://doi.org/10.1002/chin.200327046openalex-snapshot
A Copper‐Catalyzed C—N Bond Formation Involving sp‐Hybridized Carbons. Direct Entry to Chiral Ynamides via N‐Alkynylation of Amides.
inferredcites →https://doi.org/10.1002/chin.200643041openalex-snapshot
Copper(II)‐Catalyzed Amidations of Alkynyl Bromides as a General Synthesis of Ynamides and (Z)‐Enamides. An Intramolecular Amidation for the Synthesis of Macrocyclic Ynamides.
inferredcites →https://doi.org/10.1002/chin.200734047openalex-snapshot
Regio‐ and Diastereoselective Decarboxylative Coupling of Heteroaromatic Alkanes.
inferredcites →https://doi.org/10.1002/ejoc.200400865openalex-snapshot
Transition Metal Catalyzed Decarboxylative Additions of Enolates
inferredcites →https://doi.org/10.1007/3418_039openalex-snapshot
Palladium-Catalyzed Oxidation Reactions: Comparison of Benzoquinone and Molecular Oxygen as Stoichiometric Oxidants
inferredcites →https://doi.org/10.1016/j.ccr.2004.09.014openalex-snapshot
Copper in cross-coupling reactions
inferredcites →https://doi.org/10.1016/j.tet.2007.06.008openalex-snapshot
1-Protected 5-amido 1,2,3-triazoles via ruthenium-catalyzed [3+2] cycloaddition of azides and ynamides
inferredcites →https://doi.org/10.1016/j.tetlet.2008.01.073openalex-snapshot
Highly efficient synthesis of α-amino amidines from ynamides by the Cu-catalyzed three-component coupling reactions
inferredcites →https://doi.org/10.1016/s0040-4020(01)00681-0openalex-snapshot
Recent advances in the chemistry of ynamines and ynamides
inferredcites →https://doi.org/10.1021/ar800036sopenalex-snapshot
Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
inferredcites →https://doi.org/10.1021/ar800098popenalex-snapshot
Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides
inferredcites →https://doi.org/10.1021/cr020628nopenalex-snapshot
Dioxygen Activation at Mononuclear Nonheme Iron Active Sites: Enzymes, Models, and Intermediates
inferredcites →https://doi.org/10.1021/cr050523vopenalex-snapshot
Recent Advances in Transition Metal Catalyzed Oxidation of Organic Substrates with Molecular Oxygen
inferredcites →https://doi.org/10.1021/cr050992xopenalex-snapshot
The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry
inferredcites →https://doi.org/10.1021/ja021304jopenalex-snapshot
A Copper-Catalyzed C−N Bond Formation Involving sp-Hybridized Carbons. A Direct Entry to Chiral Ynamides via N-Alkynylation of Amides
inferredcites →https://doi.org/10.1021/ja027523mopenalex-snapshot
Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates
inferredcites →https://doi.org/10.1021/ja029452xopenalex-snapshot
An Exceptionally Mild Catalytic Thioester Aldol Reaction Inspired by Polyketide Biosynthesis
inferredcites →https://doi.org/10.1021/ja045981kopenalex-snapshot
Decarboxylative Aldol Reactions of Allyl β-Keto Esters via Heterobimetallic Catalysis
inferredcites →https://doi.org/10.1021/ja052099lopenalex-snapshot
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/ja0542688openalex-snapshot
Catalytic Decarboxylative sp−sp 3 Coupling
inferredcites →https://doi.org/10.1021/ja060348fopenalex-snapshot
Enantioselective Synthesis of Axially Chiral Anilides through Rhodium-Catalyzed [2+2+2] Cycloaddition of 1,6-Diynes with Trimethylsilylynamides
inferredcites →https://doi.org/10.1021/ja063115xopenalex-snapshot
Synthesis of Homoallylic Amines via the Palladium-Catalyzed Decarboxylative Coupling of Amino Acid Derivatives
inferredcites →https://doi.org/10.1021/ja063511fopenalex-snapshot
Unexpected Intermolecular Pd-Catalyzed Cross-Coupling Reaction Employing Heteroaromatic Carboxylic Acids as Coupling Partners
inferredcites →https://doi.org/10.1021/ja070116wopenalex-snapshot
Regio- and Diastereoselective Decarboxylative Coupling of Heteroaromatic Alkanes
inferredcites →https://doi.org/10.1021/ja077406xopenalex-snapshot
Copper-Catalyzed Aerobic Oxidative Amidation of Terminal Alkynes: Efficient Synthesis of Ynamides
inferredcites →https://doi.org/10.1021/ja801742hopenalex-snapshot
Asymmetric Cycloadditions of Palladium-Polarized Aza-o-xylylenes
inferredcites →https://doi.org/10.1021/ja8050926openalex-snapshot
Decarboxylative Biaryl Synthesis from Aromatic Carboxylates and Aryl Triflates
inferredcites →https://doi.org/10.1021/ja8100598openalex-snapshot
Palladium-Catalyzed Intramolecular Direct Arylation of Benzoic Acids by Tandem Decarboxylation/C−H Activation
inferredcites →https://doi.org/10.1021/ja900805yopenalex-snapshot
Nickel-Catalyzed Decarboxylative Carboamination of Alkynes with Isatoic Anhydrides
inferredcites →https://doi.org/10.1021/ja900946hopenalex-snapshot
Stereoselective Synthesis of Multisubstituted Enamides via Rhodium-Catalyzed Carbozincation of Ynamides
inferredcites →https://doi.org/10.1021/ja900984xopenalex-snapshot
Synthesis of Aromatic Esters via Pd-Catalyzed Decarboxylative Coupling of Potassium Oxalate Monoesters with Aryl Bromides and Chlorides
inferredcites →https://doi.org/10.1021/jo001044topenalex-snapshot
The Synthesis and Chemoselective Reactivity of 3-Aminocyclopentadienones
inferredcites →https://doi.org/10.1021/jo060230hopenalex-snapshot
Copper(II)-Catalyzed Amidations of Alkynyl Bromides as a General Synthesis of Ynamides and Z-Enamides. An Intramolecular Amidation for the Synthesis of Macrocyclic Ynamides
inferredcites →https://doi.org/10.1021/jo801935bopenalex-snapshot
Irregularities in the Effect of Potassium Phosphate in Ynamide Synthesis
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/jo900595copenalex-snapshot
Iron-Catalyzed Amidation of Alkynyl Bromides: A Facile Route for the Preparation of Ynamides
inferredcites →https://doi.org/10.1021/ol035647dopenalex-snapshot
Copper-Mediated N-Alkynylation of Carbamates, Ureas, and Sulfonamides. A General Method for the Synthesis of Ynamides
inferredcites →https://doi.org/10.1021/ol049827eopenalex-snapshot
Copper Sulfate-Pentahydrate-1,10-Phenanthroline Catalyzed Amidations of Alkynyl Bromides. Synthesis of Heteroaromatic Amine Substituted Ynamides
inferredcites →https://doi.org/10.1021/ol0707362openalex-snapshot
A Rhodium(I)-Catalyzed Demethylation−Cyclization of o-Anisole-Substituted Ynamides in the Synthesis of Chiral 2-Amido Benzofurans
inferredcites →https://doi.org/10.1021/ol7019394openalex-snapshot
Ir-Catalyzed Regio- and Enantioselective Decarboxylative Allylic Alkylations
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/ol801257jopenalex-snapshot
A Highly Stereoselective Synthesis of Chiral α-Amino-β-lactams via the Kinugasa Reaction Employing Ynamides
inferredcites →https://doi.org/10.1021/ol802477dopenalex-snapshot
Application of Ynamides in the Synthesis of 2-Amidoindoles
inferredcites →https://doi.org/10.1021/ol802844zopenalex-snapshot
Synthesis of Amidines Using N-Allyl Ynamides. A Palladium-Catalyzed Allyl Transfer through an Ynamido−π-Allyl Complex
inferredcites →https://doi.org/10.1038/nchem.131openalex-snapshot
A unique approach to aldol products for the creation of all-carbon quaternary stereocentres
inferredcites →https://doi.org/10.1039/a905898bopenalex-snapshot
Stereospecific synthesis of chiral N-(ethynyl)allylglycines and their use in highly stereoselective intramolecular Pauson–Khand reactions
inferredcites →https://doi.org/10.1039/b005636gopenalex-snapshot
Chemo- and regioselective crossed alkyne cyclotrimerisation of 1,6-diynes with terminal monoalkynes mediated by Grubbs’ catalyst or Wilkinson’s catalyst
inferredcites →https://doi.org/10.1039/b820291eopenalex-snapshot
First total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant
inferredcites →https://doi.org/10.1055/s-2003-40817openalex-snapshot
In Search of an Atom-EconomicalSynthesis of Chiral Ynamides
inferredcites →https://doi.org/10.1055/s-2003-42473openalex-snapshot
Renaissance of Ullmann and Goldberg Reactions - Progress in Copper Catalyzed C-N-, C-O- and C-S-Coupling
inferredcites →https://doi.org/10.1126/science.1128684openalex-snapshot
Synthesis of Biaryls via Catalytic Decarboxylative Coupling
inferredcites →https://doi.org/10.3987/rev-04-575openalex-snapshot
Synthesis and Reactions of N-Ethynyl-heterocycles

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4887161openalex-extracted
Nhc-Silver Complexes as Effective Catalysts for the Synthesis of Propiolic Acids by Reaction of Alkynes with Co2
inferred← citeshttps://doi.org/10.1002/0471264229.os096.13openalex-snapshot
Discussion Addendum for: Synthesis of Ynamides by Copper‐Mediated Coupling of 1,1‐Dibromo‐1‐Alkenes with Nitrogen Nucleophiles. Preparation of 4‐Methyl‐N‐(2‐Phenylethynyl)‐N‐(Phenylmethyl)Benzenesulfonamide
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02878.pub5openalex-snapshot
Copper( II ) Chloride
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02878.pub6openalex-snapshot
Copper( II ) Chloride
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02878.pub7openalex-snapshot
Copper( II ) Chloride
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07541.pub5openalex-snapshot
Oxygen
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07541.pub6openalex-snapshot
Oxygen
inferred← citeshttps://doi.org/10.1002/9780471264194.fos07541.pub7openalex-snapshot
Oxygen
inferred← citeshttps://doi.org/10.1002/9781118690659.ch5openalex-snapshot
Beyond Ullmann–Goldberg Chemistry: Vinylation, Alkynylation, and Allenylation of Heteronucleophiles
inferred← citeshttps://doi.org/10.1002/9783527651733.ch7openalex-snapshot
Oxidation
inferred← citeshttps://doi.org/10.1002/9783527680092.ch4openalex-snapshot
Reactions Involving Elimination of CO 2 and Ketones
inferred← citeshttps://doi.org/10.1002/9783527826186.ch10openalex-snapshot
Recent Advances in the Synthesis of Arylamines in the Light of Application in Pharmaceutical and Chemical Industry
inferred← citeshttps://doi.org/10.1002/9783527826445.ch14openalex-snapshot
Copper‐Catalyzed Decarboxylative Coupling
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.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.201300078openalex-snapshot
Palladium‐Catalyzed Decarboxylative Coupling of α‐ Oxocarboxylic Acids with C(sp2)H of 2‐Aryloxypyridines
inferred← citeshttps://doi.org/10.1002/adsc.201600516openalex-snapshot
Copper‐Catalyzed C–N, C–O Coupling Reaction of Arylglyoxylic Acids with Isatins
inferred← citeshttps://doi.org/10.1002/adsc.201700533openalex-snapshot
Palladium‐Catalyzed Cross‐Coupling of Alkynyl Carboxylic Acids with Isocyanides: Solvent‐Controlled Selective Synthesis of 5‐Iminofuranones and 5‐Iminopyrrolones
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
inferred← citeshttps://doi.org/10.1002/adsc.201901013openalex-snapshot
Regio‐ and Stereoselective Synthesis of 2‐Hydroxymethyl‐1,3‐enynes by Rhodium‐Catalyzed Decarboxylative C−C Coupling
inferred← citeshttps://doi.org/10.1002/adsc.202100211openalex-snapshot
Decarboxylation‐Initiated Intermolecular Carbon‐Heteroatom Bond Formation
inferred← citeshttps://doi.org/10.1002/ajoc.201300128openalex-snapshot
Copper‐Catalyzed N‐Alkynylation of N‐tert‐Butyloxycarbonyl (Boc)‐Protected Indoles
inferred← citeshttps://doi.org/10.1002/ajoc.201402088openalex-snapshot
Decarboxylative CP Coupling of o‐Nitrobenzoic Acids with H‐Phosphonates
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.201900110openalex-snapshot
Divergent Reactions between Alkynes and Dibenzenesulfonimide: Selective Synthesis of Ynamides and Enamides under Metal‐Free Conditions
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.202200505openalex-snapshot
CuI Catalyzed Regio‐ and Stereo‐selective Hydroboration of Ynamides: α‐ and β‐Borylation via Hydro‐Cupration and Borylation
inferred← citeshttps://doi.org/10.1002/ange.201106451openalex-snapshot
Palladium‐Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
inferred← citeshttps://doi.org/10.1002/ange.201200153openalex-snapshot
A General Pd‐Catalyzed Decarboxylative Cross‐Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds
inferred← citeshttps://doi.org/10.1002/ange.201407336openalex-snapshot
Synthesis of Bis(indole) Alkaloids from Arundo donax: The Ynindole Diels–Alder Reaction, Conformational Chirality, and Absolute Stereochemistry
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.201812068openalex-snapshot
Decarboxylative ipso Amination of Activated Benzoic Acids
inferred← citeshttps://doi.org/10.1002/ange.201912518openalex-snapshot
Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids
inferred← citeshttps://doi.org/10.1002/anie.201106451openalex-snapshot
Palladium‐Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
inferred← citeshttps://doi.org/10.1002/anie.201200153openalex-snapshot
A General Pd‐Catalyzed Decarboxylative Cross‐Coupling Reaction between Aryl Carboxylic Acids: Synthesis of Biaryl Compounds
inferred← citeshttps://doi.org/10.1002/anie.201407336openalex-snapshot
Synthesis of Bis(indole) Alkaloids from Arundo donax: The Ynindole Diels–Alder Reaction, Conformational Chirality, and Absolute Stereochemistry
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.201812068openalex-snapshot
Decarboxylative ipso Amination of Activated Benzoic Acids
inferred← citeshttps://doi.org/10.1002/anie.201912518openalex-snapshot
Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids
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/asia.201601098openalex-snapshot
Synthesis of Trifluoromethylthiolated Alkenes and Ketones by Decarboxylative Functionalization of Cinnamic Acids
inferred← citeshttps://doi.org/10.1002/asia.202300987openalex-snapshot
CuI/DMAP‐Catalyzed Oxidative Alkynylation of 7‐Azaindoles: Synthetic Scope and Mechanistic Studies
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.201200592openalex-snapshot
Biorelevant Metals in Sustainable Metal Catalysis—A Survey
inferred← citeshttps://doi.org/10.1002/cctc.201902400openalex-snapshot
Metal‐Free Oxidative Decarboxylative Heteroannulation of Alkynyl Carboxylic Acids with Sulfinates and tert‐Butyl Nitrite toward 2,2‐Disulfonyl‐2H‐Azirines
inferred← citeshttps://doi.org/10.1002/cctc.202000156openalex-snapshot
N‐Heterocyclic Carbene/Cobalt Cooperative Catalysis for the Chemo‐ and Regioselective C−N Bond Formation between Aldehyde and Amines/Amides
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/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.201501710openalex-snapshot
Ynamide Carbopalladation: A Flexible Route to Mono‐, Bi‐ and Tricyclic Azacycles
inferred← citeshttps://doi.org/10.1002/chem.201503298openalex-snapshot
Iodine‐Catalyzed Decarboxylative Amidation of β,γ‐Unsaturated Carboxylic Acids with Chloramine Salts Leading to Allylic Amides
inferred← citeshttps://doi.org/10.1002/chem.202402124openalex-snapshot
Electrochemical Decarboxylative Cross‐Coupling with Nucleophiles
inferred← citeshttps://doi.org/10.1002/chin.201039048openalex-snapshot
ChemInform Abstract: Cu‐Catalyzed Oxidative Amidation of Propiolic Acids under Air via Decarboxylative Coupling.
inferred← citeshttps://doi.org/10.1002/cjoc.201300155openalex-snapshot
Easy One‐Pot Synthesis of 1‐Monosubstituted Aliphatic 1,2,3‐Triazoles from Aliphatic Halides, Sodium Azide and Propiolic Acid by a Click Cycloaddition/Decarboxylation Process
inferred← citeshttps://doi.org/10.1002/cjoc.201700472openalex-snapshot
Reoxidation of Transition‐metal Catalysts with O2
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.201200120openalex-snapshot
A General Synthesis of Indole‐3‐carboxylic Esters by Palladium‐Catalyzed Direct Oxidative Carbonylation of 2‐Alkynylaniline Derivatives
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.201301815openalex-snapshot
Copper‐Catalyzed Decarboxylative Methylation of Aromatic Carboxylic Acids with PhI(OAc)2
inferred← citeshttps://doi.org/10.1002/ejoc.201402278openalex-snapshot
Palladium‐Catalyzed Decarboxylative C–H Bond Arylation of Furans
inferred← citeshttps://doi.org/10.1002/ejoc.201403234openalex-snapshot
Nickel‐Catalyzed Decarboxylative Arylation of Heteroarenes through sp2 C–H Functionalization
inferred← citeshttps://doi.org/10.1002/ijch.201000039openalex-snapshot
Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.1002/ppsc.201800557openalex-snapshot
Metal–Organic Framework Supported Palladium Nanoparticles: Applications and Mechanisms
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.202102494openalex-snapshot
Copper‐Catalyzed Decarboxylative Cycloaddition of Alkynyl Carboxylic Acids and Sodium Azide with Epoxides and Ethers
inferred← citeshttps://doi.org/10.1002/slct.202103035openalex-snapshot
Recent Advancement in the Copper Mediated Synthesis of Heterocyclic Amides as Important Pharmaceutical and Agrochemicals
inferred← citeshttps://doi.org/10.1002/slct.202203605openalex-snapshot
Ag(I)‐Promoted Decarboxylative Annulation of Alkynoic Acids towards 2‐Arylimidazo[1,2‐ a ]pyridines
inferred← citeshttps://doi.org/10.1002/tcr.202100030openalex-snapshot
Trends and Prospects in UiO‐66 Metal‐Organic Framework for CO 2 Capture, Separation, and Conversion
inferred← citeshttps://doi.org/10.1007/3418_2012_44openalex-snapshot
Decarboxylative Coupling Reactions
inferred← citeshttps://doi.org/10.1007/978-3-319-00702-1_4openalex-snapshot
Approach Toward the Total Synthesis of Lundurines
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/s10904-020-01643-1openalex-snapshot
One-Pot Green Synthesis of AgNPs@RGO for Removal of Water Pollutant and Chemical Fixation of CO2 Under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1007/s11426-011-4381-0openalex-snapshot
Transition metal-catalyzed decarboxylative cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00108-9openalex-snapshot
Alkynylnitrogen and -Phosphorus Compounds
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.02.012openalex-snapshot
Copper-catalyzed decarboxylative hydroboration of phenylpropiolic acids under ligand-free or both ligand- and base-free conditions
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.crci.2016.12.002openalex-snapshot
The anionic chemistry of ynamides: A review
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.jcis.2022.07.043openalex-snapshot
Nitrogen-doped mesoporous carbon single crystal-based Ag nanoparticles for boosting mild CO2 conversion with terminal alkynes
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.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.2013.03.061openalex-snapshot
Synthesis of pyrrole-2,3,4,5-tetracarboxylates via a copper-catalyzed reaction of amine with but-2-ynedioate
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.085openalex-snapshot
Development of a palladium-catalyzed decarboxylative cross-coupling of (2-azaaryl)carboxylates with aryl halides
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.073openalex-snapshot
Metal-catalyzed synthesis of hetero-substituted alkenes and alkynes
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.2015.05.115openalex-snapshot
Iodine-promoted decarboxylative C–S cross-coupling of cinnamic acids with sodium benzene sulfinates
inferred← citeshttps://doi.org/10.1016/j.tet.2016.01.042openalex-snapshot
Decarboxylative sulfonylation of arylpropiolic acids with sulfinic acids: synthesis of (E)-vinyl sulfones
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.2016.09.031openalex-snapshot
One-pot synthesis of α-acyloxycarbonyl compounds via oxidative decarboxylation coupling reaction of α-oxo carboxylic acids with carbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.tet.2019.01.009openalex-snapshot
Diverse synthesis of pyrimido[1,2-a]benzimidazoles and imidazo[2,1-b]benzothiazoles via CuI-catalyzed decarboxylic multicomponent reactions of heterocyclic azoles, aldehydes and alkynecarboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tet.2019.06.035openalex-snapshot
Mukaiyama reagent-promoted metal-free preparation of alkynyl sulfones and phosphonates under mild conditions
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.2012.09.092openalex-snapshot
Copper-catalyzed coupling of 1,2-dibromo-1-styrenes with sulfonamides for the preparation of ynamides
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.2014.12.085openalex-snapshot
CuSO4-mediated decarboxylative C–N cross-coupling of aromatic carboxylic acids with amides and anilines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.142openalex-snapshot
Metal-free multicomponent coupling reaction of aliphatic amines, formaldehyde, organoboronic acids, and propiolic acids for the synthesis of diverse propargylamines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.027openalex-snapshot
Synthesis of conjugated multi-ynamides by copper-catalyzed reactions
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.2018.01.012openalex-snapshot
One-pot synthesis of 1-monosubstituted-1, 2, 3-triazoles from 2-methyl-3-butyn-2-ol
inferred← citeshttps://doi.org/10.1021/acs.accounts.5c00142openalex-snapshot
Fundamental Principles in Catalysis from Mechanistic Studies of Oxidative Decarboxylative Coupling 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.joc.1c00101openalex-snapshot
Ligand-Enabled Copper-Catalyzed N-Alkynylation of Sulfonamide with Alkynyl Benziodoxolone: Synthesis of Amino Acid-Derived Ynamide
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.5b00558openalex-snapshot
Iron/Copper Co-Catalyzed Synthesis of Vinyl Sulfones from Sulfonyl Hydrazides and Alkyne Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00056openalex-snapshot
Amides Enable Room-Temperature CO2 Conversion: Simple Organic Molecules Challenging Metal Catalysts
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00970openalex-snapshot
Base-Mediated Intramolecular Decarboxylative Synthesis of Alkylamines from Alkanoyloxycarbamates
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01080openalex-snapshot
Advances in Decarboxylative Oxidative Coupling Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03192openalex-snapshot
Transition-Metal-Free One-Step Synthesis of Ynamides
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01408openalex-snapshot
Regioselective Pd-Catalyzed Carbopalladation/Decarboxylative Allylic Alkynylation of ortho-Iodoallenamides with Alkynyl Carboxylic Acids
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.orglett.3c01637openalex-snapshot
Copper-Catalyzed Asymmetric Cyanation of Propargylic Radicals via Direct Decarboxylation of Propargylic Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00574openalex-snapshot
β-Ketophosphonate Formation via Aerobic Oxyphosphorylation of Alkynes or Alkynyl Carboxylic Acids with H-Phosphonates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01560openalex-snapshot
Copper-/Silver-Mediated Arylation of C(sp2)–H Bonds with 2-Thiophenecarboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01859openalex-snapshot
Stereoselective Synthesis of (2Z)-2,4-Dienamides via NBS-Mediated Allyloxyl Addition–Claisen Rearrangement–Dehydrobromination Cascade Reaction of Ynsulfonamides
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.5c03692openalex-snapshot
Introducing N-Carboxyethyl-Ynamides, Precursors of Metalated Ketenimines: Protecting Group Swap in Ynamides and Olefination of Aldehydes
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02724openalex-snapshot
Palladium-Catalyzed Decarboxylative Synthesis of Arylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00013openalex-snapshot
Base-Promoted Decarboxylative Azo-Coupling: Construction of Unsymmetrical Azocarboranes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03665openalex-snapshot
A Robust One-Step Approach to Ynamides
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/acsami.5c10868openalex-snapshot
Noble-Metal-Free Cu(I)-Catalyzed sp and sp2 C–H Carboxylation to Produce High-Value Compounds via CO2 Fixation under Atmospheric Conditions
inferred← citeshttps://doi.org/10.1021/acscatal.5c08600openalex-snapshot
Ligand-Enabled Cp E Rh III -Catalyzed C( sp 3 )–H Alkynylation of Carboxamides
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/acscatal.9b04110openalex-snapshot
Intermediacy of Copper(I) under Oxidative Conditions in the Aerobic Copper-Catalyzed Decarboxylative Thiolation of Benzoic Acids
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/cr400628sopenalex-snapshot
Recent Advances in Transition-Metal-Catalyzed Functionalization of Unstrained Carbon–Carbon Bonds
inferred← citeshttps://doi.org/10.1021/ja304539jopenalex-snapshot
Decarboxylative Etherification of Aromatic Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/ja306211qopenalex-snapshot
Metal-Free Iodine(III)-Promoted Direct Intermolecular C–H Amination Reactions of Acetylenes
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/jacs.7b07546openalex-snapshot
Photoinduced, Copper-Catalyzed Decarboxylative C–N Coupling to Generate Protected Amines: An Alternative to the Curtius Rearrangement
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/jo200780xopenalex-snapshot
N-Allyl-N-sulfonyl Ynamides as Synthetic Precursors to Amidines and Vinylogous Amidines. An Unexpected N-to-C 1,3-Sulfonyl Shift in Nitrile Synthesis
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/jo5010845openalex-snapshot
Copper-Catalyzed Aerobic Decarboxylative Sulfonylation of Cinnamic Acids with Sodium Sulfinates: Stereospecific Synthesis of ( E )-Alkenyl Sulfones
inferred← citeshttps://doi.org/10.1021/jo501314yopenalex-snapshot
Copper-Catalyzed Decarboxylative Sulfonylation of α,β-Unsaturated Carboxylic 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/jo5029198openalex-snapshot
Cu-Catalyzed Aerobic Oxidative Three-Component Coupling Route to N -Sulfonyl Amidines via an Ynamine Intermediate
inferred← citeshttps://doi.org/10.1021/ol101322kopenalex-snapshot
Copper-Catalyzed Alkynylation of Amides with Potassium Alkynyltrifluoroborates: A Room-Temperature, Base-Free Synthesis of Ynamides
inferred← citeshttps://doi.org/10.1021/ol101418dopenalex-snapshot
Copper-Catalyzed Ficini [2 + 2] Cycloaddition of Ynamides
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/ol102158nopenalex-snapshot
Pd-Catalyzed Dearboxylative Heck Coupling with Dioxygen as the Terminal Oxidant
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/ol200269hopenalex-snapshot
Metal-Free Halonium Mediated Acetate Shifts of Ynamides To Access α-Halo Acrylamides/Acrylimides
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/ol200812yopenalex-snapshot
Regio- and Stereoselective Synthesis of 2-Amino-1,3-diene Derivatives by Ruthenium-Catalyzed Coupling of Ynamides and Ethylene
inferred← citeshttps://doi.org/10.1021/ol2032152openalex-snapshot
Copper-Catalyzed Oxidative Alkynylation of Diaryl Imines with Terminal Alkynes: A Facile Synthesis of Ynimines
inferred← citeshttps://doi.org/10.1021/ol303474aopenalex-snapshot
Synthesis of 3-Alkyl- or 3-Allenyl-2-amidobenzofurans via Electrophilic Cyclization of o-Anisole-Substituted Ynamides with Carbocations
inferred← citeshttps://doi.org/10.1021/ol400197yopenalex-snapshot
Copper Catalyzed Decarboxylative Alkynylation of Quaternary α-Cyano Acetate Salts
inferred← citeshttps://doi.org/10.1021/ol400213fopenalex-snapshot
A Formal Metal-Free N-Arylation via the Schmidt Reaction of Aromatic Aldehydes with an Azido Amine
inferred← citeshttps://doi.org/10.1021/ol401139mopenalex-snapshot
A New Strategy for the Construction of α-Amino Acid Esters via Decarboxylation
inferred← citeshttps://doi.org/10.1021/ol4013298openalex-snapshot
Intramolecular Carbocupration of N-Aryl-ynamides: A Modular Indole Synthesis
inferred← citeshttps://doi.org/10.1021/ol4013712openalex-snapshot
Copper-Catalyzed Nondecarboxylative Cross Coupling of Alkenyltrifluoroborate Salts with Carboxylic Acids or Carboxylates: Synthesis of Enol Esters
inferred← citeshttps://doi.org/10.1021/ol403106eopenalex-snapshot
Copper-Catalyzed Oxidative Decarboxylative Couplings of Sulfoximines and Aryl Propiolic Acids
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/10.1021/ol500749hopenalex-snapshot
Exploring the Anionic Reactivity of Ynimines, Useful Precursors of Metalated Ketenimines
inferred← citeshttps://doi.org/10.1021/ol5016898openalex-snapshot
Copper-CatalyzedN-Alkynylations of Sulfoximines with Bromoacetylenes
inferred← citeshttps://doi.org/10.1021/ol5022433openalex-snapshot
Hypervalent Iodine(III)-Mediated Oxidative Decarboxylation of β,γ-Unsaturated Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/om3005614openalex-snapshot
Copper-Mediated Selective Cross-Coupling of 1,1-Dibromo-1-alkenes and Heteronucleophiles: Development of General Routes to Heterosubstituted Alkynes and Alkenes
inferred← citeshttps://doi.org/10.1021/om300683copenalex-snapshot
The Complementary Competitors: Palladium and Copper in C–N Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1039/9781849739634-00581openalex-snapshot
7.8. Green Synthesis of Aromatic Ketones: Decarboxylative Palladium Catalysis Under Microwave Irradiation
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/c0dt01234copenalex-snapshot
Pd-catalyzed decarboxylative arylation of silyl enol ester sp3β-C–H bond under aerobic conditions
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/c2cc31159copenalex-snapshot
Heterogeneously catalyzed selective aerobic oxidative cross-coupling of terminal alkynes and amides with simple copper(ii) hydroxide
inferred← citeshttps://doi.org/10.1039/c2cs15224jopenalex-snapshot
Recent advances in transition-metal catalyzed reactions using molecular oxygen as the oxidant
inferred← citeshttps://doi.org/10.1039/c2jm35512dopenalex-snapshot
Preparation of reusable Ag-decorated graphene oxide catalysts for decarboxylative cycloaddition
inferred← citeshttps://doi.org/10.1039/c2ob26727fopenalex-snapshot
Synthesis of allenamides by Pd-catalyzed coupling of 3-alkoxycarbonyloxy ynamides or 1-alkoxycarbonyloxy allenamides with arylboronic acids
inferred← citeshttps://doi.org/10.1039/c2sc00842dopenalex-snapshot
Click-alkynylation of N- and P-nucleophiles by oxidative cross-coupling with alkynylcopper reagents: a general synthesis of ynamides and alkynylphosphonates
inferred← citeshttps://doi.org/10.1039/c2sc20606dopenalex-snapshot
Copper-catalyzed decarboxylative C–N coupling for N-arylation
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/c3cc48069kopenalex-snapshot
Silver catalyzed decarboxylative direct C2-alkylation of benzothiazoles with carboxylic acids
inferred← citeshttps://doi.org/10.1039/c3ob41408fopenalex-snapshot
Synthesis of substituted nitroolefins: a copper catalyzed nitrodecarboxylation of unsaturated carboxylic 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/c4cc03198aopenalex-snapshot
Turning unreactive copper acetylides into remarkably powerful and mild alkyne transfer reagents by oxidative umpolung
inferred← citeshttps://doi.org/10.1039/c4cc05720aopenalex-snapshot
Revealing the halide effect on the kinetics of the aerobic oxidation of Cu( i ) to Cu( ii )
inferred← citeshttps://doi.org/10.1039/c4cc07876dopenalex-snapshot
A robust and modular synthesis of ynamides
inferred← citeshttps://doi.org/10.1039/c4cs00239copenalex-snapshot
Recent advances in C–S bond formation via C–H bond functionalization and decarboxylation
inferred← citeshttps://doi.org/10.1039/c4ra12782jopenalex-snapshot
A Cu-catalysed synthesis of substituted 3-methyleneisoindolin-1-one
inferred← citeshttps://doi.org/10.1039/c4sc00265bopenalex-snapshot
MOF catalysis in relation to their homogeneous counterparts and conventional solid catalysts
inferred← citeshttps://doi.org/10.1039/c5cc05084gopenalex-snapshot
Highly selective copper-catalyzed trifunctionalization of alkynyl carboxylic acids: an efficient route to bis-deuterated β-borylated α,β-styrene
inferred← citeshttps://doi.org/10.1039/c5cc09179aopenalex-snapshot
Silver-catalyzed oxidative decarboxylation of difluoroacetates: efficient access to C–CF 2 bond formation
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
showing the first 200 of 248 · page through all 248
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.