On the public citation graph

Selective oxymetalation of terminal alkynes via 6- endo cyclization: mechanistic investigation and application to the efficient synthesis of 4-substituted isocoumarins

0 signed · 146 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/adsc.201000810openalex-snapshot
Highly Selective Palladium‐Catalyzed Direct CH α‐Monoarylation of Carbonyl Compounds using Water Containing the Surfactant Polyoxyethylene‐α‐Tocopheryl Sebacate (PTS) as a Solvent
inferredcites →https://doi.org/10.1002/ajoc.201200100openalex-snapshot
2‐Alkynylbenzaldehyde: A Versatile Building Block for the Generation of Cyclic Compounds
inferredcites →https://doi.org/10.1002/ajoc.201600602openalex-snapshot
Theoretical Investigation on the ClBcat‐Promoted Synthesis of Heterocyclic Boronic Esters
inferredcites →https://doi.org/10.1002/anie.200901417openalex-snapshot
Regio‐ and Stereoselective Generation of Alkenylindium Compounds from Indium Tribromide, Alkynes, and Ketene Silyl Acetals
inferredcites →https://doi.org/10.1002/anie.201103409openalex-snapshot
Characterization of the Isochromen‐4‐yl‐gold(I) Intermediate in the Gold(I)‐Catalyzed Glycosidation of Glycosyl ortho‐Alkynylbenzoates and Enhancement of the Catalytic Efficiency Thereof
inferredcites →https://doi.org/10.1002/anie.201106132openalex-snapshot
Characterization of Vinylgold Intermediates: Gold‐Mediated Cyclization of Acetylenic Amides
inferredcites →https://doi.org/10.1002/anie.201203914openalex-snapshot
Catalytic Generation of Zinc Carbenes from Alkynes: Zinc‐Catalyzed Cyclopropanation and SiH Bond Insertion Reactions
inferredcites →https://doi.org/10.1002/anie.201608090openalex-snapshot
Catalyst‐Free Formal Thioboration to Synthesize Borylated Benzothiophenes and Dihydrothiophenes
inferredcites →https://doi.org/10.1002/anie.201610014openalex-snapshot
BCl3‐Induced Annulative Oxo‐ and Thioboration for the Formation of C3‐Borylated Benzofurans and Benzothiophenes
inferredcites →https://doi.org/10.1002/anie.201612243openalex-snapshot
C,O‐Chelated BINOL/Gold(III) Complexes: Synthesis and Catalysis with Tunable Product Profiles
inferredcites →https://doi.org/10.1002/chem.201102255openalex-snapshot
Carbogallation of Alkynes Using Gallium Tribromide and Silyl Ketene Acetals and Synthetic Application to Cross‐Coupling with Aryl Iodides
inferredcites →https://doi.org/10.1002/chem.201300232openalex-snapshot
Gold‐Catalyzed Reactions of Enynals/Enynones with Norbornenes: Generation and Trapping of Cyclic o‐Quinodimethanes (o‐QDMs)
inferredcites →https://doi.org/10.1002/chem.201500648openalex-snapshot
Highly Stereoselective β‐Mannopyranosylation via the 1‐α‐Glycosyloxy‐isochromenylium‐4‐gold(I) Intermediates
inferredcites →https://doi.org/10.1002/ejic.201402678openalex-snapshot
Cyclizations of Aryl Enynes Containing Propargyl Alcohol and Diallylamine Groups to Yield Indolecarbaldehydes Induced by Ruthenium Complexes
inferredcites →https://doi.org/10.1002/ejoc.200900865openalex-snapshot
Pd‐Catalyzed Reactions of Allenylphosphonates and Related Allenes with Functionalized 2‐Iodophenols, 2‐Iodobenzoic Acid, and 2‐Iodobenzyl Alcohol Leading to Functionalized Benzofurans, Isocoumarins, and Benzopyrans
inferredcites →https://doi.org/10.1002/ejoc.201201656openalex-snapshot
How to Lose a Bond in Two Ways ― The Diradical/Zwitterion Dichotomy in Cycloaromatization Reactions
inferredcites →https://doi.org/10.1002/hlca.201300239openalex-snapshot
Synthesis of 4‐Arylisocoumarins (=4‐Aryl‐1H‐2‐benzopyran‐1‐ones) through Acidic Hydrolysis of (Z)‐2‐(1‐Aryl‐2‐methoxyethenyl)benzaldehydes, Followed by Oxidation
inferredcites →https://doi.org/10.1002/jlac.198119810507openalex-snapshot
Synthesen von Fluoreszenzfarbstoffen, 11 über die Umlagerung von Alkoxymethylen‐ und Aminomethylenhomophthalsäureanhydriden zu Isocumarinen bzw. Isochinolinonen
inferredcites →https://doi.org/10.1002/jlac.199719970130openalex-snapshot
Secondary Fungal Metabolites and Their Biological Activity, VIII. – Partial Synthesis of Oosponol, an Antifungal Isocoumarin
inferredcites →https://doi.org/10.1002/jlac.199719970422openalex-snapshot
Total Synthesis of the Toxin Oosponol and of Structural Analogues and Investigation of Their Antibiotic Activities
inferredcites →https://doi.org/10.1002/wcms.1261openalex-snapshot
The Baldwin rules: revised and extended
inferredcites →https://doi.org/10.1007/978-3-030-12858-6openalex-snapshot
Progress in the Chemistry of Organic Natural Products 109
inferredcites →https://doi.org/10.1016/j.bmc.2007.11.038openalex-snapshot
Structural insights into hydroxycoumarin-induced apoptosis in U-937 cells
inferredcites →https://doi.org/10.1016/j.bmcl.2006.04.087openalex-snapshot
Anti-HIV activity of stilbene-related heterocyclic compounds
inferredcites →https://doi.org/10.1016/j.jorganchem.2010.09.062openalex-snapshot
ZnCl2-catalyzed [4 + 2] benzannulation of 2-ethynylbenzaldehydes with alkynes: Selective synthesis of naphthalene derivatives
inferredcites →https://doi.org/10.1016/j.jorganchem.2014.01.028openalex-snapshot
Intramolecular heterocyclization and cyclopalladation of selenoanisole substituted propargyl imines: Synthesis and reactivity of Pd–C bond towards alkynes
inferredcites →https://doi.org/10.1016/j.poly.2013.06.010openalex-snapshot
Directing the regioselectivity of rhodium(I) catalysed cyclisation of 2-alkynyl benzoic acids
inferredcites →https://doi.org/10.1016/j.tet.2007.07.066openalex-snapshot
Cycloisomerization of γ- and δ-acetylenic acids catalyzed by gold(I) chloride
inferredcites →https://doi.org/10.1016/j.tetlet.2018.01.014openalex-snapshot
PtCl4-catalyzed cyclization of N-acetyl-2-alkynylanilines: A mild and efficient synthesis of N-acetyl-2-substituted indoles
inferredcites →https://doi.org/10.1016/s0022-328x(01)01328-6openalex-snapshot
Synthesis of 2-pyranylidene or (2-furyl)carbene–chromium complexes from conjugated enyne carbonyl compounds with Cr(CO)5(THF)
inferredcites →https://doi.org/10.1016/s0031-9422(00)85513-2openalex-snapshot
Polygonolide, an isocoumarin from Polygonum hydropiper possessing anti-inflammatory activity
inferredcites →https://doi.org/10.1016/s0031-9422(00)89017-2openalex-snapshot
The identification of lenzitin as oosponol
inferredcites →https://doi.org/10.1016/s0040-4020(01)90889-0openalex-snapshot
The photochemistry of iminium salts and related heteroaromatic systems
inferredcites →https://doi.org/10.1016/s0040-4020(01)92039-3openalex-snapshot
A theoretical investigation of α-substituents on the structure, proton affinities and inversion barriers of silyl anions
inferredcites →https://doi.org/10.1016/s0040-4039(01)81355-1openalex-snapshot
Reactions of 2-acylbenzoates with dimethyloxosulphonium methylide: A novel route to isocoumarins
inferredcites →https://doi.org/10.1016/s0040-4039(01)81446-5openalex-snapshot
Une synthese originale et inattendue d'isocoumarines fonctionnelles
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00057openalex-snapshot
Organic Photoredox Catalysis
inferredcites →https://doi.org/10.1021/acs.joc.5b02602openalex-snapshot
Synthesis of Isocoumarins via Silver(I)-Mediated Annulation of Enol Esters
inferredcites →https://doi.org/10.1021/acs.joc.6b01948openalex-snapshot
Gold-Catalyzed β-Regioselective Formal [3 + 2] Cycloaddition of Ynamides with Pyrido[1,2-b]indazoles: Reaction Development and Mechanistic Insights
inferredcites →https://doi.org/10.1021/acs.joc.7b00198openalex-snapshot
Silver-Catalyzed Cyclization of ortho-Carbonylarylacetylenols for the Synthesis of Dihydronaphthofurans
inferredcites →https://doi.org/10.1021/acs.joc.7b01500openalex-snapshot
Mechanistic Studies of Formal Thioboration Reactions of Alkynes
inferredcites →https://doi.org/10.1021/acs.orglett.5b03530openalex-snapshot
Oxyboration with and without a Catalyst: Borylated Isoxazoles via B–O σ-Bond Addition
inferredcites →https://doi.org/10.1021/acscatal.6b02636openalex-snapshot
Gold-Catalyzed Access to 1H-Isochromenes: Reaction Development and Mechanistic Insight
inferredcites →https://doi.org/10.1021/ar020258popenalex-snapshot
Strategies for Heterocyclic Construction via Novel Multicomponent Reactions Based on Isocyanides and Nucleophilic Carbenes
inferredcites →https://doi.org/10.1021/ar700094bopenalex-snapshot
Asymmetric Hydrogenation of Heteroaromatic Compounds
inferredcites →https://doi.org/10.1021/cc049879vopenalex-snapshot
The Recent Impact of Solid-Phase Synthesis on Medicinally Relevant Benzoannelated Oxygen Heterocycles
inferredcites →https://doi.org/10.1021/cr00075a005openalex-snapshot
Five-membered heteroaromatic rings as intermediates in organic synthesis
inferredcites →https://doi.org/10.1021/cr00094a006openalex-snapshot
Cycloaddition reactions of heteroaromatic six-membered rings
inferredcites →https://doi.org/10.1021/cr0200872openalex-snapshot
Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis
inferredcites →https://doi.org/10.1021/cr0201068openalex-snapshot
Transition-Metal-Catalyzed Addition of Heteroatom−Hydrogen Bonds to Alkynes
inferredcites →https://doi.org/10.1021/cr050041jopenalex-snapshot
Coinage Metal-Assisted Synthesis of Heterocycles
inferredcites →https://doi.org/10.1021/cr500691kopenalex-snapshot
Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity
inferredcites →https://doi.org/10.1021/cr60229a002openalex-snapshot
Isocoumarins. Developments Since 1950
inferredcites →https://doi.org/10.1021/cr990327mopenalex-snapshot
Quantitative Measures of Aromaticity for Mono-, Bi-, and Tricyclic Penta- and Hexaatomic Heteroaromatic Ring Systems and Their Interrelationships
inferredcites →https://doi.org/10.1021/cs400437sopenalex-snapshot
Gold Catalysis 2.0
inferredcites →https://doi.org/10.1021/ic50011a013openalex-snapshot
Crystal and Molecular Structure of Indium(III) Iodide (In 2 I 6 )
inferredcites →https://doi.org/10.1021/ja00327a026openalex-snapshot
Mercury in organic chemistry. 26. Synthesis of heterocycles via intramolecular solvomercuration of aryl acetylenes
inferredcites →https://doi.org/10.1021/ja010478iopenalex-snapshot
Generation and Reaction of Metal-Containing Carbonyl Ylides: Tandem [3+2]-Cycloaddition−Carbene Insertion Leading to Novel Polycyclic Compounds
inferredcites →https://doi.org/10.1021/ja017366bopenalex-snapshot
Pd(II) Acts Simultaneously as a Lewis Acid and as a Transition-Metal Catalyst: Synthesis of Cyclic Alkenyl Ethers from Acetylenic Aldehydes
inferredcites →https://doi.org/10.1021/ja044194kopenalex-snapshot
Generation and Reaction of Tungsten-Containing Carbonyl Ylides: [3 + 2]-Cycloaddition Reaction with Electron-Rich Alkenes
inferredcites →https://doi.org/10.1021/ja203191fopenalex-snapshot
Rules for Anionic and Radical Ring Closure of Alkynes
inferredcites →https://doi.org/10.1021/ja4058844openalex-snapshot
Palladium-Catalyzed Carbene Migratory Insertion Using Conjugated Ene–Yne–Ketones as Carbene Precursors
inferredcites →https://doi.org/10.1021/ja4064316openalex-snapshot
Mechanistic Insights into the Gold(I)-Catalyzed Activation of Glycosyl ortho -Alkynylbenzoates for Glycosidation
inferredcites →https://doi.org/10.1021/ja500463popenalex-snapshot
Alkoxyboration: Ring-Closing Addition of B–O σ Bonds across Alkynes
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jacs.5b06678openalex-snapshot
Aminoboration: Addition of B–N σ Bonds across C–C π Bonds
inferredcites →https://doi.org/10.1021/jacs.5b12989openalex-snapshot
Catalyst-Free Synthesis of Borylated Lactones from Esters via Electrophilic Oxyboration
inferredcites →https://doi.org/10.1021/jacs.6b13168openalex-snapshot
Catalytic B–H Bond Insertion Reactions Using Alkynes as Carbene Precursors
inferredcites →https://doi.org/10.1021/jm200338aopenalex-snapshot
Systematic Enumeration of Heteroaromatic Ring Systems as Reagents for Use in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/jo010789bopenalex-snapshot
Synthesis of 4-Acetylisocoumarin: First Total Syntheses of AGI-7 and Sescandelin
inferredcites →https://doi.org/10.1021/jo034308vopenalex-snapshot
Synthesis of Isocoumarins and α-Pyrones via Electrophilic Cyclization
inferredcites →https://doi.org/10.1021/jo0352732openalex-snapshot
Catalytic Cyclopropanation of Alkenes via (2-Furyl)carbene Complexes from 1-Benzoyl-cis-1-buten-3-yne with Transition Metal Compounds
inferredcites →https://doi.org/10.1021/jo049416bopenalex-snapshot
Synthesis of Cyclic Alkenyl Ethers via Intramolecular Cyclization of O-Alkynylbenzaldehydes. Importance of Combination between CuI Catalyst and DMF
inferredcites →https://doi.org/10.1021/jo061525yopenalex-snapshot
Palladium-Catalyzed Coupling of Allenylphosphonates, Phenylallenes, and Allenyl Esters: Remarkable Salt Effect and Routes to Novel Benzofurans and Isocoumarins
inferredcites →https://doi.org/10.1021/jo800474copenalex-snapshot
Indium(III)-Catalyzed Tandem Reaction with Alkynylbenzaldehydes and Alkynylanilines to Heteroaromatic Compounds
inferredcites →https://doi.org/10.1021/np200885eopenalex-snapshot
Phthalide and Isocoumarin Derivatives Produced by an Acremonium sp. Isolated from a Mangrove Rhizophora apiculata
inferredcites →https://doi.org/10.1021/ol034731qopenalex-snapshot
Doyle−Kirmse Reaction of Allylic Sulfides with Diazoalkane-Free (2-Furyl)carbenoid Transfer
inferredcites →https://doi.org/10.1021/ol0364024openalex-snapshot
Platinum(II)-Catalyzed Reaction of 2-Alkynylbenzoates or Benzothioates with Vinyl Ethers: A Concise Method for Synthesis of 1-Acyl-4-alkoxy- or 1-Acyl-4-alkylsulfanylnaphthalene Derivatives
inferredcites →https://doi.org/10.1021/ol0530427openalex-snapshot
Directed Ortho-Metalation of Unprotected Benzoic Acids. Methodology and Regioselective Synthesis of Useful Contiguously 3- and 6-Substituted 2-Methoxybenzoic Acid Building Blocks
inferredcites →https://doi.org/10.1021/ol062476eopenalex-snapshot
Palladium-Catalyzed Oxidative Activation of Arylcyclopropanes
inferredcites →https://doi.org/10.1021/ol300718xopenalex-snapshot
Pd- and Cu-Catalyzed One-Pot Multicomponent Synthesis of Hetero α,α′-Dimers of Heterocycles
inferredcites →https://doi.org/10.1021/ol5021256openalex-snapshot
Silver-Catalyzed Domino Hydroarylation/Cycloisomerization Reactions of ortho-Alkynylbenzaldehydes: An Entry to Functionalized Isochromene Derivatives
inferredcites →https://doi.org/10.1021/om040063gopenalex-snapshot
Equilibrium between η2-(o-Ethynylbenzoyl)rhenium Complexes and Rhenium Isobenzofuryl Carbene Complexes and Subsequent Reactions of Isobenzofuryl Carbene Complexes
inferredcites →https://doi.org/10.1021/om300030eopenalex-snapshot
Deconvolution of the Mechanism of Homogeneous Gold-Catalyzed Reactions
inferredcites →https://doi.org/10.1038/nrd1549openalex-snapshot
Docking and scoring in virtual screening for drug discovery: methods and applications
inferredcites →https://doi.org/10.1039/c29710000921openalex-snapshot
The synthesis of oosponol and oospoglycol
inferredcites →https://doi.org/10.1039/c3cc43872dopenalex-snapshot
Finding the right path: Baldwin “Rules for Ring Closure” and stereoelectronic control of cyclizations
inferredcites →https://doi.org/10.1039/c3cc46524aopenalex-snapshot
Silver-catalyzed cascade cyclization–stannylation of o-alkynylaniline derivatives with 2-tributylstannylfuran: an efficient synthesis of (3-indolyl)stannanes
inferredcites →https://doi.org/10.1039/c4ra17066kopenalex-snapshot
Intramolecular cyclization assisted oxidative addition: synthesis of octahedral cycloplatinated methyl complexes
inferredcites →https://doi.org/10.1039/c5ce02397aopenalex-snapshot
Experimental electron densities of neutral and zwitterionic forms of the drug piroxicam
inferredcites →https://doi.org/10.1039/c6cs00465bopenalex-snapshot
Transition metal-catalyzed cross-coupling reactions using organoindium reagents
inferredcites →https://doi.org/10.1055/s-0033-1339190openalex-snapshot
Rhodium-Catalyzed Reaction of 2H-Azirines with Carbonyl-ene-yne Compounds Giving 1-Furyl-2-aza-1,3-dienes
inferredcites →https://doi.org/10.1055/s-2000-6321openalex-snapshot
Total Synthesis of RS-42358 and Analogs Using Lateral Lithiation
inferredcites →https://doi.org/10.1111/j.1432-1033.1997.t01-2-00045.xopenalex-snapshot
Influence of the Gloeophyllum Metabolite Oosponol and Some Synthetic Analogues on Protein and RNA Synthesis in Target Cells
inferredcites →https://doi.org/10.1142/p464openalex-snapshot
Atoms, Molecules and Clusters in Electric Fields
inferredcites →https://doi.org/10.1158/0008-5472.can-04-2626openalex-snapshot
2-(8-Hydroxy-6-methoxy-1-oxo-1Η-2-benzopyran-3-yl)propionic Acid, a Small Molecule Isocoumarin, Potentiates Dexamethasone-Induced Apoptosis of Human Multiple Myeloma Cells
inferredcites →https://doi.org/10.1248/cpb.29.2689openalex-snapshot
Antifungal activity of oosponol, oospolactone, phyllodulcin, hydrangenol, and some other related compounds.
inferredcites →https://doi.org/10.1248/cpb.42.2225openalex-snapshot
Development of Bioactive Functions in Hydrangeae Dulcis Folium. III. On the Antiallergic and Antimicrobial Principles of Hydrangeae Dulcis Folium. (1). Thunberginols A, B, and F.
inferredcites →https://doi.org/10.1254/jjp.28.693openalex-snapshot
Inhibition of Compound 48/80-Mediated Histamine Release from Isolated Rat Mast Cells by Oosponol-Related Compounds (4-Acyl-Isocoumarins).
inferredcites →https://doi.org/10.15227/orgsyn.093.0228openalex-snapshot
Oxyboration: Synthesis of Borylated Benzofurans
inferredcites →https://doi.org/10.7164/antibiotics.52.426openalex-snapshot
Inhibition of Angiogenesis by a New Isocoumarin, NM-3.
inferredcites →https://doi.org/10.7164/antibiotics.54.463openalex-snapshot
Anti-angiogenic Activities of Novel Isocoumarins, AGI-7 and Sescandelin.

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.4055499openalex-extracted
inferred← citeshttps://doi.org/10.1002/adsc.201801507openalex-snapshot
Palladium/Acid Relay Catalyzed Tandem Heck Coupling/6‐Endo Cyclization between ortho‐Halogenated Benzoates and Unactivated Terminal Alkenes for the Synthesis of 1‐Isochromanones
inferred← citeshttps://doi.org/10.1002/adsc.201900764openalex-snapshot
Ruthenium(II)‐Catalyzed Homocoupling of Weakly Coordinating Sulfoxonium Ylides via C−H Activation/Annulations: Synthesis of Functionalized Isocoumarins
inferred← citeshttps://doi.org/10.1002/adsc.202000125openalex-snapshot
Divergent Palladium‐Catalyzed Tandem Reaction of Cyanomethyl Benzoates with Arylboronic Acids: Synthesis of Oxazoles and Isocoumarins
inferred← citeshttps://doi.org/10.1002/adsc.202000313openalex-snapshot
Fe(III)‐Catalyzed, Cyclizative Coupling between 2‐Alkynylbenzoates and Carbinols: Rapid Generation of Polycyclic Isocoumarins and Phthalides and Mechanistic Study
inferred← citeshttps://doi.org/10.1002/adsc.202301329openalex-snapshot
Stereospecific Indium(III)‐Catalysed Tandem Cycloisomerization of Functionalized 1,6‐enynes: Scope and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/adsc.70638openalex-snapshot
Rhodium‐Catalyzed Cascade Synthesis of 3,4‐Disubstituted Isocoumarins From Ortho‐Alkynylbenzoates and Diazo Compounds
inferred← citeshttps://doi.org/10.1002/ange.202402370openalex-snapshot
Alkoxycarbonyl Groups in Metalloesters Showing Oxocarbenium‐like Structure and Alkylating Reactivity
inferred← citeshttps://doi.org/10.1002/anie.202402370openalex-snapshot
Alkoxycarbonyl Groups in Metalloesters Showing Oxocarbenium‐like Structure and Alkylating Reactivity
inferred← citeshttps://doi.org/10.1002/asia.201901730openalex-snapshot
Carbometalation and Heterometalation of Carbon‐Carbon Multiple‐Bonds Using Group‐13 Heavy Metals: Carbogallation, Carboindation, Heterogallation, and Heteroindation
inferred← citeshttps://doi.org/10.1002/chem.201905175openalex-snapshot
Synthesis of (Z)‐β‐(Carbonylamino)alkenylindium through Regioselective anti‐Carboindation of Ynamides and Its Transformation to Multisubstituted Enamides
inferred← citeshttps://doi.org/10.1002/chem.202001766openalex-snapshot
Continuous Electrochemical Synthesis of Iso‐Coumarin Derivatives from o‐(1‐Alkynyl) Benzoates under Metal‐ and Oxidant‐Free
inferred← citeshttps://doi.org/10.1002/chem.202100672openalex-snapshot
Indium‐Catalyzed C−F Bond Transformation through Oxymetalation/β‐Fluorine Elimination to Access Fluorinated Isocoumarins
inferred← citeshttps://doi.org/10.1002/chem.202202284openalex-snapshot
Synthesis of Cage‐Shaped Borates Bearing Pyrenylmethyl Groups: Efficient Lewis Acid Catalyst for Photoactivated Glycosylations Driven by Intramolecular Excimer Formation
inferred← citeshttps://doi.org/10.1002/ejoc.202300925openalex-snapshot
Metal‐Free Synthesis of 4‐Bromoisocoumarins through Brominative Annulation of 2‐Alkynylaryloate Esters Using In Situ Generated Transient Bromoiodane
inferred← citeshttps://doi.org/10.1002/slct.202201791openalex-snapshot
Total Synthesis of AGI‐7 and Sescandelin from Enol Esters
inferred← citeshttps://doi.org/10.1007/978-981-16-2458-2_13openalex-snapshot
Reaction Field for a Lewis Acid with a Tunable Factor for Selective Organic Synthesis
inferred← citeshttps://doi.org/10.1007/s10593-026-03441-yopenalex-snapshot
Synthetic strategies for 4-aroylisochromen-1-ones and isoquinolin-1-ones (microreview)
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00082-5openalex-snapshot
Vinyl and Aryl Metals
inferred← citeshttps://doi.org/10.1016/bs.adomc.2023.02.001openalex-snapshot
Indium organometallics in transition metal-catalyzed cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128392openalex-snapshot
Design, synthesis and biological evaluation of new thiazole scaffolds as potential TRPM8 antagonists
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133740openalex-snapshot
Recent advances in synthesis of isocoumarins: An overview
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152724openalex-snapshot
Rhodium-catalyzed oxidative coupling of benzoic acids with propargyl alcohols: An efficient access to isocoumarins
inferred← citeshttps://doi.org/10.1016/j.trechm.2021.05.005openalex-snapshot
Main-group metalated heterocycles through Lewis acid cyclization
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00825openalex-snapshot
Indium(III)-Catalyzed Stereoselective Synthesis of Tricyclic Frameworks by Cascade Cycloisomerization Reactions of Aryl 1,5-Enynes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03077openalex-snapshot
Regioselective Synthesis of Isocoumarins via Iridium(III)-Catalyzed Oxidative Cyclization of Aromatic Acids with Propargyl Alcohols
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01505openalex-snapshot
Regio- and Stereoselective Carboindation of Internal Alkynyl Ethers with Organosilicon or -stannane Nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02186openalex-snapshot
Regioselective Synthesis of 5-Metalated 2-Pyrones by Intramolecular Oxymetalation of Carbonyl-ene-yne Compounds Using Indium Trihalide
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02793openalex-snapshot
Metal-Free Synthesis of 4-Chloroisocoumarins by TMSCl-Catalyzed NCS-Induced Chlorinative Annulation of 2-Alkynylaryloate Esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02112openalex-snapshot
Concise Synthesis of Isocoumarins through Rh-Catalyzed Direct Vinylene Annulation: Scope and Mechanistic Insight
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02851openalex-snapshot
Synthesis of 4-Alkylated Isocoumarins via Pd-Catalyzed α-Arylation Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01008openalex-snapshot
Palladium-Catalyzed 1,1-Alkynyloxygenation of 2-Vinylbenzoates with Alkynyl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03028openalex-snapshot
A Synthesis of 4-(Hydroxymethyl)-1H-isochromen-1-one Analogs by Hydroxyl Oxetane Rearrangement in Protonic Acids
inferred← citeshttps://doi.org/10.1021/acscatal.0c00220openalex-snapshot
Gold(I) or Gold(III) as Real Intermediate Species in Gold-Catalyzed Cycloaddition Reactions of Enynal/Enynone?
inferred← citeshttps://doi.org/10.1021/acsomega.5c07356openalex-snapshot
Synthesis and Fluorescent Properties of Alkynylated 3-Methylidenephthalides with Extended π-Systems
inferred← citeshttps://doi.org/10.1021/jacs.4c08291openalex-snapshot
Total Synthesis of Ganoapplanin Enabled by a Radical Addition/Aldol Reaction Cascade
inferred← citeshttps://doi.org/10.1039/d1ob01065dopenalex-snapshot
Modular synthesis of 3-substituted isocoumarins via silver-catalyzed aerobic oxidation/ 6-endo heterocyclization of ortho -alkynylbenzaldehydes
inferred← citeshttps://doi.org/10.1039/d3nj02073hopenalex-snapshot
Rh( iii )-catalyzed cascade annulation reaction of N , N -dimethyl enaminones with iodonium ylides to give substituted isocoumarins
inferred← citeshttps://doi.org/10.1039/d3nj04361dopenalex-snapshot
Access to derivatives of 4-(arylthio)isocoumarins via hydrogen bonding network assisted electrophilic cyclization
inferred← citeshttps://doi.org/10.1055/a-2109-0183openalex-snapshot
Ruthenium(II)-Catalyzed C–H Annulation of Mandelic Acids with Internal Alkynes to Construct Isocoumarins
inferred← citeshttps://doi.org/10.1055/a-2114-7582openalex-snapshot
Halogenative Annulation Reactions of Alkyne-Tethered N- and O-Containing Arenes: Methods for Accessing Aryl-Fused Halogenated N- and O-Heterocycles
inferred← citeshttps://doi.org/10.1055/a-2818-3037openalex-snapshot
Brønsted Acid-Mediated Synthesis of Isocoumarins and Isoquinolines
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.80.1000openalex-snapshot
Lewis Acid-mediated Carbon-Fluorine Bond Transformation: Substitution of Fluorine and Insertion into a Carbon-Fluorine Bond
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.80.14openalex-snapshot
Development of Carbometalation and Oxymetalation by Using Moderate Lewis Acidity and π-Electrophilic Affinity of Heavy Main-group Metals
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.