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Atom Economy. Palladium-Catalyzed Formation of Coumarins by Addition of Phenols and Alkynoates via a Net C−H Insertion

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

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Enolether, XVIII Eine einfache Synthese von Cumarinen
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A new synthesis of coumarins
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Synthetical experiments in the chromone group—XXXV
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Extractives of Dalea species (Leguminosae)
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Synthetic application of lithiation reactions—VII
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A novel synthesis of 2,6-disubstituted and 2,3,6-trisubstituted anilines
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Chemistry of dibenzylideneacetone-palladium(0) complexes
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Acridone alkaloids and a coumarin from Citrus grandis
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A novel regio- and stereo-specific hydroacetoxylation reaction of 2-alkynoic acid derivatives
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Palladium-catalyzed aryloxycarbonylation of terminal alkynes
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Palladium(II) catalyzed cyclization of alkynoic acids
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Synthesis of the coumarin, toddaculin
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Neue cumarine aus pelargonium reniforme curt.-wurzel
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Anti-AIDS agents-XXVIII.1 Synthesis and Anti-HIV activity of methoxy substituted 3′,4′-Di-O-(−)-camphanoyl-(+)-cis-khellactone (DCK) analogues
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Chemoprevention of carcinogen-DNA binding: the relative role of different oxygenated substituents on 4-methylcoumarins in the inhibition of aflatoxin B1-DNA binding in vitro
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Rare-Earth Metal Triflates in Organic Synthesis
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A New Palladium-Catalyzed Addition: A Mild Method for the Synthesis of Coumarins
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Anti-AIDS Agents. 37. Synthesis and Structure−Activity Relationships of (3‘R,4‘R)-(+)-cis-Khellactone Derivatives as Novel Potent Anti-HIV Agents
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Palladium-catalyzed reaction of vinyl triflates and vinyl/aryl halides with 4-alkynoic acids: regio- and stereoselective synthesis of (E)-.delta.-vinyl/aryl-.gamma.-methylene-.gamma.-butyrolactones
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Synthesis of highly functionalized flavones and chromones using cycloacylation reactions and C-3 functionalization. A total synthesis of hormothamnione
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New syntheses of coumarins
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New Syntheses in the Coumarin Series
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Highly Enantioenriched Propargylic Alcohols by Oxazaborolidine-Mediated Reduction of Acetylenic Ketones
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Carboindation of Carbon−Carbon Triple Bonds: Regioselective Indium-Mediated Allylation of Functionalized Alkynes and Transformation into Halogen-Substituted 1,4-Dienes
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Studies on the Indian Rutaceae. Chemical Investigation of Limonia alata and Evodia lunu-ankenda
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Xanthyletin and Xanthoxyletin from a Gorgonian, Echinogorgia sp.
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Biological Activity of Some Coumarins from Sri Lankan Rutaceae
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Antiinflammatory Activity of Coumarins fromSantolina oblongifolia
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Synthesis and Cytotoxic Activity of Pyranocoumarins of the Seselin and Xanthyletin Series
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Addition of Methanol to Nonactivated Internal Alkynes Catalyzed by Dichloro(diphosphine)platinum(II) Complex/Silver Salt Systems
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Palladium-Assisted Formation of Carbon−Carbon Bonds. 8.1 Synthesis and Reactivity toward Internal Alkynes, Carbon Monoxide, and Isocyanides of Orthopalladated Dibenzylamine Complexes
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Trimethylsilylketene: Synthesis of Coumarins via Cyclization-Elimination
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Aluminium Chloride/Phosphoryl Chloride as an Efficient Acylating Agent
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A High-Yield Method for the Methylenation of o -Dihydroxyaromatic Compounds: Synthesis of Methylenedioxycoumarins
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A Convenient Synthesis off Coumarins by Denitro-cyclization
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The constituents of Eriostemon trachyphyllus . The structure of trachyphyllin, a new coumarin
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Synthesis of evodionol and alloevodionol
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Total Synthesis of (±)-Calanolide A
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An Efficient Large Scale Synthesis of Coumarins by a Dealkylative Boron-Mediated Ring Closure of 3-(Ortho-methoxyaryl)propenoic Esters
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Efficient Activation of Aromatic C-H Bonds for Addition to C-C Multiple Bonds
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Characterization of plant coumarins by combined gas chromatography, ultraviolet absorption spectroscopy, and nuclear magnetic resonance analysis
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Bromophloroglucinols and their methyl ethers
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Synthetic Studies of Sesamol Derivatives. I. A New Synthesis of Ayapin
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Syntheses of 4-Phenylcoumarins Containing a Dimethylpyran Ring
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Studies on coumarins from the root of Angelica pubescens Maxim. III. Structures of various coumarins including angelin, a new prenylcoumarin.
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A convenient synthesis of a simple coumarin.
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Convenient Synthesis of a Simple Coumarin from Salicylaldehyde and Wittig Reagent. II : Synthesis ofBromo- and Methoxycarbonylcoumarins.
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Selected applications to organic synthesis of intramolecular C-H activation reactions by transition metals
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A Convenient Synthesis of 2,2-Dimethylchromenes from 2,2-Dimethylchromanones

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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Palladium(II) acetate
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Palladium(II) acetate
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Palladium( II ) Acetate
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Palladium( II ) Acetate
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Palladium( II ) acetate
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Palladium( II ) acetate
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Cross‐Coupling of Organyl Halides with Alkenes: the Heck Reaction
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Visible Light‐Induced Decarboxylative Acylarylation of Phenyl Propiolates with α‐Oxocarboxylic Acids to Coumarins Catalyzed by Hypervalent Iodine Reagents under Transition Metal‐Free Conditions
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Palladium‐Acid Co‐Catalyzed Cleavage of Alkynoates to Construct Dibenzo[c,h]xanthene Derivatives
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Synthesis of π‐Expanded Coumarins by Ligand‐Enabled Selective C−H Functionalization
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Base‐Promoted Direct Cascade Transformation of Chromones to Coumarins via Benzannulation and Transesterification
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Direct Access to Benzo[b]furans through Palladium‐Catalyzed Oxidative Annulation of Phenols and Unactivated Internal Alkynes
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Palladium‐Catalyzed Synthesis of Benzofurans and Coumarins from Phenols and Olefins
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An Efficient Nanoscale Heterogeneous Catalyst for the Capture and Conversion of Carbon Dioxide at Ambient Pressure
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Constructions of Biaryl‐Bridged Macrocycles Through Phosphine‐Ligand‐Controlled Switch of Selectivity Between Intra‐ and Intermolecular Cyclizations
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Direct Access to Benzo[ b ]furans through Palladium‐Catalyzed Oxidative Annulation of Phenols and Unactivated Internal Alkynes
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Reductive coupling of polyfunctionalized organobismuth and organolead arylating reagents in the synthesis of benzopyran derivatives
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Reactions of N-phenylamide and phenyl (thio)esters of 3-phenylpropiolic acid with benzene under superelectrophilic activation
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Synthetic Reactions via C–H Bond Activation: C–C and C–E Bond Formation
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Synthetic Reactions via C–H Bond Activation: Oxidation of C–H Bonds
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5.33 Hydroarylation Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-95047-3.00002-2openalex-snapshot
Coumarins and chalcones against SARS-CoV-2
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00004-0openalex-snapshot
Synthesis and reactivity
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00608-8openalex-snapshot
Pyrans and their Benzo Derivatives: Synthesis
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00923-8openalex-snapshot
Tricyclic Systems: Central Carbocyclic Ring with Fused Six-membered Rings
inferred← citeshttps://doi.org/10.1016/j.arabjc.2016.07.020openalex-snapshot
Facile synthetic approach for 5-aryl-9-hydroxypyrano [3,2-f] indole-2(8H)-one
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105222openalex-snapshot
Presegetane diterpenoids from Euphorbia sieboldiana as a new type of anti-liver fibrosis agents that inhibit TGF-β/Smad signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.06.026openalex-snapshot
Structure–activity relationship of natural and synthetic coumarins inhibiting the multidrug transporter P-glycoprotein
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.12.098openalex-snapshot
Synthesis of hydroxycoumarins and hydroxybenzo[f]- or [h]coumarins as lipid peroxidation inhibitors
inferred← citeshttps://doi.org/10.1016/j.cclet.2007.10.047openalex-snapshot
Two new coumarin glucosides biosynthesized by transgenic hairy roots of Polygonum multiflorum
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2003
inferred← citeshttps://doi.org/10.1016/j.enchem.2021.100064openalex-snapshot
Reticular frameworks and their derived materials for CO2 conversion by thermo−catalysis
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105337openalex-snapshot
Chemical constituents from the roots of Zanthoxylum bungeanum Maxim. and their neuroprotective activities
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.05.029openalex-snapshot
Multiple reactivities of dithranol towards 1-alkynyl Fischer carbene complexes (CO)5M C(OEt)C CPh (M = Cr, W) – Efficient chemical synthesis of aromatic polyketides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.07.008openalex-snapshot
A high hydroarylation activity of K2PtCl4/AgOTf catalyst in the reaction of propiolic acid with unactivated and activated arenes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.08.009openalex-snapshot
Catalytic hydroarylation of alkynes with arenes in the presence of FeCl3 and AgOTf
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2007.01.014openalex-snapshot
TiO2-catalyzed photooxygenation of cinnamic acid derivatives via their radical cations
inferred← citeshttps://doi.org/10.1016/j.mcat.2020.111319openalex-snapshot
Copper(I)-modified covalent organic framework for CO2 insertion to terminal alkynes
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112404openalex-snapshot
Recyclable palladium-catalyzed cyclocarbonylation between benzyl chlorides and salicylic aldehydes towards coumarins
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144426openalex-snapshot
Coumarins as versatile scaffolds: Innovative synthetic strategies for generating diverse heterocyclic libraries in drug discovery
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112395openalex-snapshot
Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells
inferred← citeshttps://doi.org/10.1016/j.tet.2006.04.080openalex-snapshot
Synthesis of coumarins by Pt-catalyzed hydroarylation of propiolic acids with phenols
inferred← citeshttps://doi.org/10.1016/j.tet.2006.06.079openalex-snapshot
Intramolecular electrophilic hydroarylation via Claisen rearrangement: synthesis of chromenes, heterothiochromenes and heterodihydrothiochromenes
inferred← citeshttps://doi.org/10.1016/j.tet.2007.02.075openalex-snapshot
Synthesis and biological activity of vicinal diaryl-substituted 1H-imidazoles
inferred← citeshttps://doi.org/10.1016/j.tet.2007.09.076openalex-snapshot
Highly selective hydroarylation of propiolic acid derivatives using a PtCl2/AgOTf catalytic system
inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.059openalex-snapshot
Total synthesis of naturally occurring 5,6,7- and 5,7,8-trioxygenated coumarins
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.055openalex-snapshot
An expedient route to highly functionalized 2H-chromene-2-thiones via ring annulation of β-oxodithioesters catalyzed by InCl3 under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2013.08.072openalex-snapshot
Palladium-catalyzed one-pot synthesis of benzo[b][1,6]naphthyridines via Sonogashira coupling and annulation reactions from 2-chloroquinoline-3-carbonitriles
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.032openalex-snapshot
Copper oxide catalyzed domino process for the synthesis of substituted 2H-pyran-2-ones and polyhydroxy coumarin derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.059openalex-snapshot
Pd-catalyzed chemo-selective mono-arylations and bis-arylations of functionalized 4-chlorocoumarins with triarylbismuths as threefold arylating reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134256openalex-snapshot
Pd0 catalyst/carboxylic acid-mediated hydrofunctionalization of alkynes and allenes, two plausible hydropalladation mechanisms of a versatile process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.01.097openalex-snapshot
Pd/CaCO3 in liquid poly(ethylene glycol) (PEG): an easy and efficient recycle system for partial reduction of alkynes to cis-olefins under a hydrogen atmosphere
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.02.038openalex-snapshot
Facile and selective copper–palladium catalyzed addition of terminal alkynes to activated alkynes in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.07.129openalex-snapshot
Regioselective Pd-catalyzed alkylative lactonizations of 4-hydroxy-2-alkynecarboxylates with organoboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.03.179openalex-snapshot
Efficient and selective hydroarylation of propiolic acids and their esters with arenes catalyzed by a PtCl2/AgOTf system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.133openalex-snapshot
A novel synthesis of coumarins employing triphenyl(α-carboxymethylene)phosphorane imidazolide as a C-2 synthon
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.134openalex-snapshot
Catalytic synthesis of novel 4-C-glycosyl coumarins using a domino Heck reaction/lactonization process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.130openalex-snapshot
Iron(III)-catalyzed hydroarylation of propiolic acid with activated arenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.082openalex-snapshot
Synthesis of 4-arylcoumarins via palladium-catalyzed arylation/cyclization of ortho-hydroxylcinnamates with diaryliodonium salts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.034openalex-snapshot
Diterpenoids and phenanthrenones from the leaves and stems of Strophioblachia fimbricalyx
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.06.039openalex-snapshot
Metal-free, Brønsted acid-mediated synthesis of coumarin derivatives from phenols and propiolic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.062openalex-snapshot
New method for the synthesis of chromeno[4,3-b]chromene derivatives via multicomponent reaction promoted by niobium pentachloride
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151917openalex-snapshot
Facile synthesis and characterization of indene-fused 4-methylcoumarins and an unexpected skeletal rearrangement via Pechmann condensation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155099openalex-snapshot
Visible-light photocatalysed synthesis of coumarin derivatives
inferred← citeshttps://doi.org/10.1016/s0959-6380(05)80057-1openalex-snapshot
Chapter 6.4 Six-membered ring systems: With O and/or S atoms
inferred← citeshttps://doi.org/10.1016/s0959-6380(99)80018-xopenalex-snapshot
Chapter 6.4 Six-Membered Ring Systems: With O and/or S Atoms
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00571openalex-snapshot
Green and Sustainable Solvents in Chemical Processes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c00905openalex-snapshot
Interfacial Electron Modulation of AgxCuy@ZIF-8 for Photothermally Catalyzing CO2 Organic Transformations
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02011openalex-snapshot
Gold(I)-Catalyzed Intramolecular Hydroarylation of Phenol-Derived Propiolates and Certain Related Ethers as a Route to Selectively Functionalized Coumarins and 2H-Chromenes
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01187openalex-snapshot
Pd-Catalyzed Alkyne and Aryne Annulations: Synthesis and Photophysical Properties of π-Extended Coumarins
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00316openalex-snapshot
Ru(II)-Catalyzed Oxidative Spiroannulation of 2-Arylphenols with Alkynes via a C–H Activation/Dearomatization Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01713openalex-snapshot
Rh-Catalyzed Synthesis of Coumarin Derivatives from Phenolic Acetates and Acrylates via C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00608openalex-snapshot
Sustainable Synthesis of 3-Acylmethylated Coumarins via Photoredox Catalytic Radical Addition/Cyclization in Aqueous Media
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02094openalex-snapshot
Vertically π-Expanded Coumarins: The Synthesis and Optical Properties
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03051openalex-snapshot
Palladium(II)-Catalyzed Intramolecular C–H Alkenylation for the Synthesis of Chromanes
inferred← citeshttps://doi.org/10.1021/acs.organomet.7b00649openalex-snapshot
Stereo- and Regioselective Addition of Arene to Alkyne Using Abnormal NHC Based Palladium Catalysts: Elucidating the Role of Trifluoroacetic Acid in Fujiwara Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02130openalex-snapshot
A Bifunctional Ligand Enables Gold-Catalyzed Hydroarylation of Terminal Alkynes under Soft Reaction Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00364openalex-snapshot
Access to Coumarins by Rhodium-Catalyzed Oxidative Annulation of Aryl Thiocarbamates with Internal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02391openalex-snapshot
Intermolecular Synthesis of Coumarins from Acid Chlorides and Unactivated Alkynes through Palladium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01214openalex-snapshot
Rhenium-Catalyzed Regioselective ortho-Alkenylation and [3 + 2 + 1] Cycloaddition of Phenols with Internal Alkynes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03882openalex-snapshot
Sequential Energy Transfer Catalysis: A Cascade Synthesis of Angularly-Fused Dihydrocoumarins
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03932openalex-snapshot
Pd(II)-Catalyzed Oxidative Annulation via Double C–H Activations: Synthesis and Photophysical Properties of Bis-Coumarins
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04355openalex-snapshot
Asymmetric Total Synthesis and Biological Evaluation of the Natural PDE4 Inhibitor Toddacoumalone
inferred← citeshttps://doi.org/10.1021/acsaem.6c01952openalex-snapshot
Solar C(sp)–H Carboxylation: Silver-Embedded Covalent Organic Framework Film as a Highly Efficient Photocatalyst for Carboxylation of C(sp)–H Bonds with CO2 under Solar Light
inferred← citeshttps://doi.org/10.1021/acsami.3c16690openalex-snapshot
Pyrene-Based Nanoporous Covalent Organic Framework for Carboxylation of C–H Bonds with CO2 and Value-Added 2-Oxazolidinones Synthesis under Ambient Conditions
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/acsanm.4c05173openalex-snapshot
Construction of Porous Organic Polymer Coordinated Palladium Nanoparticle Catalysts for Catalytic Synthesis of Coumarin Derivatives
inferred← citeshttps://doi.org/10.1021/acscatal.4c06006openalex-snapshot
Photocatalytic Carboxylation of Terminal Alkynes with CO 2 over Metal–Porphyrin Framework Nanosheets
inferred← citeshttps://doi.org/10.1021/acscatal.6c00211openalex-snapshot
Switchable Divergent Synthesis of Inherently Chiral Calixarenes via Palladium-Catalyzed Asymmetric Hydroarylation of Alkynes
inferred← citeshttps://doi.org/10.1021/acscatal.8b04098openalex-snapshot
Phenol-Directed C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acsinfecdis.8b00325openalex-snapshot
Derivatives of Natural Product Agrimophol as Disruptors of Intrabacterial pH Homeostasis in Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1021/acsomega.1c03469openalex-snapshot
Pd(II)-Catalyzed Fujiwara–Moritani Reactions for the Synthesis and Functionalization of Substituted Coumarins
inferred← citeshttps://doi.org/10.1021/acsomega.9b02489openalex-snapshot
One-Pot Synthesis of 4-Carboalkoxy-Substituted Benzo[ h ]coumarins from α- and β-Naphthols and Their Excited-State Properties
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/cs300448vopenalex-snapshot
Catalytic C–H Carboxylation of Terminal Alkynes with Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/ja410060eopenalex-snapshot
RuII-Catalyzed Vinylative Dearomatization of Naphthols via a C(sp2)–H Bond Activation Approach
inferred← citeshttps://doi.org/10.1021/jacs.5b05843openalex-snapshot
Rh-Catalyzed Construction of Quinolin-2(1H)-ones via C–H Bond Activation of Simple Anilines with CO and Alkynes
inferred← citeshttps://doi.org/10.1021/jacs.5b12081openalex-snapshot
One Photocatalyst, n Activation Modes Strategy for Cascade Catalysis: Emulating Coumarin Biosynthesis with (−)-Riboflavin
inferred← citeshttps://doi.org/10.1021/jo301086kopenalex-snapshot
Synthesis of Substituted Coumarins via Brønsted Acid Mediated Condensation of Allenes with Substituted Phenols or Anisoles
inferred← citeshttps://doi.org/10.1021/jo401583qopenalex-snapshot
Total Syntheses of the Coumarin-Containing Natural Products Pimpinellin and Fraxetin Using Au(I)-Catalyzed Intramolecular Hydroarylation (IMHA) Chemistry
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/jo802285ropenalex-snapshot
An Efficient Carbene-Catalyzed Access to 3,4-Dihydrocoumarins
inferred← citeshttps://doi.org/10.1021/jo901314topenalex-snapshot
Selective Synthesis of 3-Aryl Quinolin-2(1H)-ones and 3-(1-Arylmethylene)oxindoles Involving a 2-Fold Arene C−H Activation Process
inferred← citeshttps://doi.org/10.1021/jo901855popenalex-snapshot
Domino Heck/Lactonization-Catalyzed Synthesis of 3-C-Linked Mannopyranosyl Coumarins
inferred← citeshttps://doi.org/10.1021/jo901963gopenalex-snapshot
Palladium-Catalyzed Intramolecular 5-exo-dig Hydroarylations of N-Arylpropiolamides: Thermodynamics-Controlled Stereoselective Synthesis of 3-Methyleneoxindoles
inferred← citeshttps://doi.org/10.1021/np401040dopenalex-snapshot
Prenylated Coumarins: Natural Phosphodiesterase-4 Inhibitors from Toddalia asiatica
inferred← citeshttps://doi.org/10.1021/ol401581popenalex-snapshot
A Catalyst-Free One-Pot Construction of Skeletons of 5-Methoxyseselin and Alloxanthoxyletin in Water
inferred← citeshttps://doi.org/10.1021/ol403028aopenalex-snapshot
Pd(II)-Catalyzed C(sp2)–H Hydroxylation with R2(O)P-Coordinating Group
inferred← citeshttps://doi.org/10.1021/ol502997dopenalex-snapshot
Palladium(II)-Catalyzed Oxidative Dearomatization of Free Naphthols with Two Alkyne Units
inferred← citeshttps://doi.org/10.1021/ol8001305openalex-snapshot
Synthesis of Amine−Borane Intramolecular Complexes through Palladium-Catalyzed Rearrangement of Ammonioalkynyltriarylborates
inferred← citeshttps://doi.org/10.1021/ol802117popenalex-snapshot
Colorimetric Test Kit for Cu2+ Detection
inferred← citeshttps://doi.org/10.1021/om7002909openalex-snapshot
Monomeric Alkoxo and Amido Methylnickel(II) Complexes. Synthesis and Heterocumulene Insertion Chemistry
inferred← citeshttps://doi.org/10.1038/nprot.2007.103openalex-snapshot
Practical and convenient synthesis of coumarins from phenols and propiolic acid esters
inferred← citeshttps://doi.org/10.1039/b407936aopenalex-snapshot
The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones
inferred← citeshttps://doi.org/10.1039/b805946mopenalex-snapshot
Palladium-catalyzed 1,4-addition of terminal alkynes to unsaturated carbonyl compounds promoted by electron-rich ligands
inferred← citeshttps://doi.org/10.1039/b810658dopenalex-snapshot
Drastic effect of bidentate phosphine ligands on Pd-catalyzed hydroarylation of ethyl propiolate: a simple route to arylbutadienes
inferred← citeshttps://doi.org/10.1039/b912887eopenalex-snapshot
Electrocyclization of cis-dienals in organic synthesis: a new and versatile synthetic method for the preparation of aryl- and heteroaryl-fused coumarins
inferred← citeshttps://doi.org/10.1039/c004233aopenalex-snapshot
One-pot synthesis of furocoumarins via sequential Pd/Cu-catalyzed alkynylation and intramolecular hydroalkoxylation
inferred← citeshttps://doi.org/10.1039/c2cc35762copenalex-snapshot
Facile carbon–sulfur bond cleavage in diarylsulfonium ylides: a catalytic sulfur-to-silicon group transfer
inferred← citeshttps://doi.org/10.1039/c2ob06884bopenalex-snapshot
A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates
inferred← citeshttps://doi.org/10.1039/c2ob07137aopenalex-snapshot
Direct C–H cross-coupling approach to heteroaryl coumarins
inferred← citeshttps://doi.org/10.1039/c2ra00820copenalex-snapshot
An unusual one-pot synthesis of 3-benzoylcoumarins and coumarin-3-carbaldehydes from 2-hydroxybenzaldehydes under esterification conditions
inferred← citeshttps://doi.org/10.1039/c2ra00987kopenalex-snapshot
InCl3 catalyzed domino route to 2H-chromene-2-ones via [4 + 2] annulation of 2-hydroxyarylaldehydes with α-oxoketene dithioacetal under solvent-free conditions
inferred← citeshttps://doi.org/10.1039/c3cc41296bopenalex-snapshot
One-pot catalysis of dehydrogenation of cyclohexanones to phenols and oxidative Heck coupling: expedient synthesis of coumarins
inferred← citeshttps://doi.org/10.1039/c3cs60369eopenalex-snapshot
Synthesis of heterocycles via transition-metal-catalyzed hydroarylation of alkynes
inferred← citeshttps://doi.org/10.1039/c3ob40859kopenalex-snapshot
Diversity-oriented general protocol for the synthesis of privileged oxygen scaffolds: pyrones, coumarins, benzocoumarins and naphthocoumarins
inferred← citeshttps://doi.org/10.1039/c3qo00010aopenalex-snapshot
Palladium-catalyzed base-accelerated direct C–H bond alkenylation of phenols to synthesize coumarin derivatives
inferred← citeshttps://doi.org/10.1039/c3ra42503gopenalex-snapshot
Novel atom-economic reaction: comprehensive utilization of S-alkylisothiouronium salt in the synthesis of thioethers and guanidinium salts
inferred← citeshttps://doi.org/10.1039/c4sc01536copenalex-snapshot
A cooperative N-heterocyclic carbene/palladium catalysis system
inferred← citeshttps://doi.org/10.1039/c4tc02665aopenalex-snapshot
π-Expanded coumarins: synthesis, optical properties and applications
inferred← citeshttps://doi.org/10.1039/c5cc00878fopenalex-snapshot
Visible-light initiated oxidative cyclization of phenyl propiolates with sulfinic acids to coumarin derivatives under metal-free conditions
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/c6cc09108copenalex-snapshot
An atom- and pot-economical consecutive multi-step reaction approach to polycyclic aromatic hydrocarbons (PAHs)
inferred← citeshttps://doi.org/10.1039/c6ob01732kopenalex-snapshot
Metal-free radical addition/cyclization of alkynoates with xanthates towards 3-(β-carbonyl)coumarins
inferred← citeshttps://doi.org/10.1039/c6ra01731bopenalex-snapshot
Palladium( ii ) oxide impregnated on magnetite as a catalyst for the synthesis of 4-arylcoumarins via a Heck-arylation/cyclization process
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/c8gc01034jopenalex-snapshot
Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols
inferred← citeshttps://doi.org/10.1039/c8gc03593hopenalex-snapshot
Metal-free synthesis of triarylated ( Z )-nitrones via H 2 O-mediated 1,3-dipolar transfer under aerobic conditions
inferred← citeshttps://doi.org/10.1039/c8ob02232aopenalex-snapshot
Visible-light-promoted radical acylation/cyclization of alkynoates with aldehydes for the synthesis of 3-acylcoumarins
inferred← citeshttps://doi.org/10.1039/c8qo00614hopenalex-snapshot
Pd( ii )-Catalyzed [3 + 2] spiroannulation of α-aryl-β-naphthols with alkynes via a C–H activation/dearomatization approach
inferred← citeshttps://doi.org/10.1039/c8tb01144copenalex-snapshot
Two-photon absorbing 8-hydroxy-benzo[ g ]coumarins with giant Stokes shifts: an environment-insensitive dye platform for probing biomolecules
inferred← citeshttps://doi.org/10.1039/c9cc00324jopenalex-snapshot
Regioselective synthesis of polycyclic sulfones via radical-induced three-component bicyclization cascades
inferred← citeshttps://doi.org/10.1039/c9gc04184bopenalex-snapshot
Thermal [2 + 2]-cycloaddition between silylalkynes and allenylphenols followed by the nucleophilic addition of water: metal-free and economical synthesis of arylcyclobutenals
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