On the public citation graph

Palladium-Catalyzed Oxidative Activation of Arylcyclopropanes

0 signed · 93 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1016/0040-4020(96)00011-7openalex-snapshot

Palladium-catalyzed annulation of vinylic cyclopropanes and cyclobutanes

inferredcites →https://doi.org/10.1016/j.tet.2004.10.077openalex-snapshot

Recent advances in donor–acceptor (DA) cyclopropanes

inferredcites →https://doi.org/10.1016/s0022-328x(00)81846-xopenalex-snapshot

Palladium(II) catalyzed rearrangement of bicyclo[6.1.0]- non-4-ene to cis,cis-1,5-cyclononadiene

inferredcites →https://doi.org/10.1016/s0022-328x(00)86635-8openalex-snapshot

Reactions of bicyclic cyclopropanes and bicyclic cyclobutanes with dichlorobis(benzonitrile)palladium(II)

inferredcites →https://doi.org/10.1016/s0040-4020(01)00777-3openalex-snapshot

Synthesis of cyclopropane containing natural products

inferredcites →https://doi.org/10.1016/s0040-4039(00)85966-3openalex-snapshot

Reaction of tetracyclo[3.3.0.02,4.03,6]oct-7-ene with HCL and DCL; successive formation of edge- and corner-protonated cyclopropanes

inferredcites →https://doi.org/10.1016/s0040-4039(01)97255-7openalex-snapshot

Protolytic cleavage of cyclopropanes: The structure of the transition state in the protonation of arylcyclopropanes

inferredcites →https://doi.org/10.1021/cr010016nopenalex-snapshot

Donor−Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis

inferredcites →https://doi.org/10.1021/ja00191a082openalex-snapshot

Definitive characterization of the C3H7+ potential energy surface

inferredcites →https://doi.org/10.1021/ja00461a019openalex-snapshot

Stereochemistry of the electrophilic ring opening of cyclopropanes. 2. Reaction of cis- and trans-1,2,3-trimethylcyclopropane with deuterium(1+) ion

inferredcites →https://doi.org/10.1021/ja00753a065openalex-snapshot

Protonation of cyclopropane

inferredcites →https://doi.org/10.1021/ja00780a062openalex-snapshot

Protonated cyclopropanes. VII. Evidence for edge protonation

inferredcites →https://doi.org/10.1021/ja00810a069openalex-snapshot

Stereochemistry of the electrophilic ring opening of cyclopropanes by deuterium(1+) ion. Evidence for an unsymmetrical, nonrotating, corner-protonated cyclopropane

inferredcites →https://doi.org/10.1021/ja00849a011openalex-snapshot

Chloropalladation of cyclopropane in bicyclo[5.1.0]oct-3-ene and subsequent 1,4,5-.eta.-cyclooctenyl to 1-3-.eta.-cyclooctenyl rearrangement

inferredcites →https://doi.org/10.1021/ja00999a046openalex-snapshot

Nuclear magnetic resonance spectroscopy. Carbon-carbon coupling in cyclopropane derivatives

inferredcites →https://doi.org/10.1021/ja055534kopenalex-snapshot

Oxidative Cyclizations in a Nonpolar Solvent Using Molecular Oxygen and Studies on the Stereochemistry of Oxypalladation

inferredcites →https://doi.org/10.1021/jo00128a046openalex-snapshot

Corner versus Edge Protonation of Cyclopropane

inferredcites →https://doi.org/10.1021/jo01313a034openalex-snapshot

Cyclopropanation of ester enolates by .pi.-allylpalladium chloride complexes

inferredcites →https://doi.org/10.1021/jo981468bopenalex-snapshot

Ring Opening in the Hydroamination of Methylenecyclopropanes Catalyzed by Palladium

inferredcites →https://doi.org/10.1021/jp973203ropenalex-snapshot

Cracking of Hydrocarbons on Zeolite Catalysts: Density Functional and Hartree−Fock Calculations on the Mechanism of the β-Scission Reaction

inferredcites →https://doi.org/10.1021/om00071a014openalex-snapshot

Chloropalladation of exo-9-methylbicyclo[6.1.0]non-4-ene. Inversion of configuration at carbon bound to palladium and at carbon bound to chlorine

inferredcites →https://doi.org/10.1021/om00126a030openalex-snapshot

Stereochemistry and mechanism of palladium(II)-induced ring opening of the cyclopropane in a vinylcyclopropane. Chloro- and oxypalladation of (+)-2-carene

inferredcites →https://doi.org/10.1021/om00136a034openalex-snapshot

Facile chloropalladation of vinylcyclopropanes. Isolation of ring-opened 1,2,5-.eta.3-.sigma.,.pi. chelates as kinetic precursors to 1-3-.eta.3-.pi.-allyl final products

inferredcites →https://doi.org/10.1039/c39820000321openalex-snapshot

Stereochemistry of palladium( II )-induced ring-opening of the cyclopropane in a vinylcyclopropane. Chloropalladation of car-2-ene

inferredcites →https://doi.org/10.1039/c39870000943openalex-snapshot

A high level ab initio study of corner-protonated cyclopropane

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/10.1002/0471264180.or084.02openalex-snapshot

Wacker Oxidation, The

inferred← citeshttps://doi.org/10.1002/9780470638859.conrr653openalex-snapshot

Wacker Oxidation

inferred← citeshttps://doi.org/10.1002/9780470669587.ch14openalex-snapshot

Molecular Rearrangements: Part 2. Other Reactions

inferred← citeshttps://doi.org/10.1002/9780471264194.fos00982.pub3openalex-snapshot

Bis(Acetonitrile)Dichloropalladium( II )

inferred← citeshttps://doi.org/10.1002/9780471264194.fos00982.pub4openalex-snapshot

Bis(Acetonitrile)Dichloropalladium( II )

inferred← citeshttps://doi.org/10.1002/9780471264194.fos00982.pub5openalex-snapshot

Bis(acetonitrile)dichloropalladium( II )

inferred← citeshttps://doi.org/10.1002/9780471264194.fos00982.pub6openalex-snapshot

Bis(acetonitrile)dichloropalladium( II )

inferred← citeshttps://doi.org/10.1002/9781119941910.ch14openalex-snapshot

Molecular Rearrangements: Part 2. Other Reactions

inferred← citeshttps://doi.org/10.1002/9783527633388.ch2openalex-snapshot

Transition Metal Catalyzed Approaches to Lactones Involving CO Bond Formation

inferred← citeshttps://doi.org/10.1002/9783527680092.ch2openalex-snapshot

Reactions of Three‐Membered Ring Compounds

inferred← citeshttps://doi.org/10.1002/adsc.201800019openalex-snapshot

Isocoumarins: General Aspects and Recent Advances in their Synthesis

inferred← citeshttps://doi.org/10.1002/ange.202412368openalex-snapshot

Selective Hydroboration of C−C Single Bonds without Transition‐Metal Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202412368openalex-snapshot

Selective Hydroboration of C−C Single Bonds without Transition‐Metal Catalysis

inferred← citeshttps://doi.org/10.1002/chin.200715137openalex-snapshot

Palladium‐Catalyzed Oxidative Activation of Arylcyclopropanes.

inferred← citeshttps://doi.org/10.1002/ejoc.201500908openalex-snapshot

Construction of Isoquinolin‐1(2H)‐ones by Copper‐Catalyzed Tandem Reactions of 2‐(1‐Alkynyl)benzaldimines with Water

inferred← citeshttps://doi.org/10.1002/ejoc.201701446openalex-snapshot

C–O Bonds from Pd‐Catalyzed C(sp3)–H Reactions Mediated by Heteroatomic Groups

inferred← citeshttps://doi.org/10.1002/slct.202201791openalex-snapshot

Total Synthesis of AGI‐7 and Sescandelin from Enol Esters

inferred← citeshttps://doi.org/10.1007/3418_2015_118openalex-snapshot

Catalytic C–H Bond Functionalization of Cyclopropane Derivatives

inferred← citeshttps://doi.org/10.1007/7081_2013_102openalex-snapshot

Synthesis of Heterocycles via Palladium-Catalyzed Wacker-Type Oxidative Cyclization Reactions of Hydroxy- and Amino-Alkenes

inferred← citeshttps://doi.org/10.1007/s11030-013-9429-yopenalex-snapshot

An efficient and expeditious synthesis of novel 2,2-dialkyl-2,3-dihydrobenzofurans from phenols and 2,2-dialkylacetaldehydes

inferred← citeshttps://doi.org/10.1007/s11164-017-3000-xopenalex-snapshot

Recent progress in insertion and cyclopropanation reactions of metal carbenoids from α-diazocarbonyl compounds

inferred← citeshttps://doi.org/10.1016/j.bmc.2012.01.035openalex-snapshot

Might the observed α2A-adrenoreceptor agonism or antagonism of allyphenyline analogues be ascribed to different molecular conformations?

inferred← citeshttps://doi.org/10.1016/j.ccr.2017.10.004openalex-snapshot

Copper nanoparticles as inexpensive and efficient catalyst: A valuable contribution in organic synthesis

inferred← citeshttps://doi.org/10.1016/j.ccr.2018.11.001openalex-snapshot

Building molecular complexity through transition-metal-catalyzed oxidative annulations/cyclizations: Harnessing the utility of phenols, naphthols and 1,3-dicarbonyl compounds

inferred← citeshttps://doi.org/10.1016/j.jaap.2022.105638openalex-snapshot

Flash vacuum pyrolysis of aryl propargyl ethers

inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.144openalex-snapshot

tert-BuOK-mediated carbanion–yne intramolecular cyclization: synthesis of 2-substituted 3-benzylbenzofurans

inferred← citeshttps://doi.org/10.1016/j.tet.2011.11.024openalex-snapshot

Facile synthesis of aryl(het)cyclopropane catalyzed by palladacycle

inferred← citeshttps://doi.org/10.1016/j.tet.2012.12.009openalex-snapshot

One-pot access to 2-naphthols and benzofurans via the aerobic Wacker-type oxidation/intramolecular aldol cyclization

inferred← citeshttps://doi.org/10.1016/j.tet.2013.02.080openalex-snapshot

Palladium-catalyzed ring-opening of cyclopropyl benzamides: synthesis of benzo[c]azepine-1-ones via C(sp3)–H functionalization

inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.090openalex-snapshot

Cyclopropanation of diazoesters with styrene derivatives catalyzed by magnetically recoverable copper-plated iron nanoparticles

inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.011openalex-snapshot

Cyclopropanation of diazoesters with styrene derivatives catalyzed by magnetically recoverable copper-plated iron nanoparticles

inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.03.004openalex-snapshot

Asymmetric conjugate addition of cis-2-arylethenylboronic acids catalyzed by chiral diene/rhodium complexes: 1,4-rhodium shift from alkenylrhodium to arylrhodium intermediates

inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.07.087openalex-snapshot

Convenient synthesis of novel 2,2-dialkyl-1,2-dihydronaphtho[2,1-b]furans

inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.12.034openalex-snapshot

Facile synthesis of 3,3-diallyl isoindolones via a indium-mediated double allylation of ortho-cyanobenzoates

inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.010openalex-snapshot

(±)-CSA catalyzed Friedel–Crafts alkylation of indoles with 3-ethoxycarbonyl-3-hydoxyisoindolin-1-one: an easy access of 3-ethoxycarbonyl-3-indolylisoindolin-1-ones bearing a quaternary α-amino acid moiety

inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot

Chapter 5.3 Five-membered ring systems: Furans and benzofurans

inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80009-8openalex-snapshot

Chapter 5.3 Five-membered ring systems: furans and benzofurans

inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70019-4openalex-snapshot

Chapter 6.4 (2006): Six-membered ring systems: with O and/or S atoms

inferred← citeshttps://doi.org/10.1021/acs.joc.1c02958openalex-snapshot

Preparation of Dihydronaphthofurans from α-Hydroxyl Ketones via a One-Pot Multicomponent Reaction Based on Heyns Rearrangement

inferred← citeshttps://doi.org/10.1021/acs.joc.5b02602openalex-snapshot

Synthesis of Isocoumarins via Silver(I)-Mediated Annulation of Enol Esters

inferred← citeshttps://doi.org/10.1021/acs.joc.8b02576openalex-snapshot

Amination of Carbenium Ions Generated by Directed Protonolysis of Cyclopropane

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00143openalex-snapshot

Electrochemical Formation of Oxazolines by 1,3-Oxyfluorination of Non-activated Cyclopropanes

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00584openalex-snapshot

Amide-Group-Directed Protonolysis of Cyclopropane: An Approach to 2,2-Disubstituted Pyrrolidines

inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03250openalex-snapshot

Phosphine-Catalyzed Asymmetric (3+2) Annulations of δ-Acetoxy Allenoates with 2-Naphthols

inferred← citeshttps://doi.org/10.1021/acscatal.6b00978openalex-snapshot

Cobalt(III)-Catalyzed [5 + 1] Annulation for 2H-Chromenes Synthesis via Vinylic C–H Activation and Intramolecular Nucleophilic Addition

inferred← citeshttps://doi.org/10.1021/cc900121copenalex-snapshot

Facile Route to 1,3-Diazaheterocycle-Fused [1,2b]Isoquinolin-1(2H)-one Derivatives via Substitution-Cyclization Reactions

inferred← citeshttps://doi.org/10.1021/jacs.0c05213openalex-snapshot

σ-Bond Hydroboration of Cyclopropanes

inferred← citeshttps://doi.org/10.1021/jo400621ropenalex-snapshot

Reactions of o-Quinone Methides with Pyridinium Methylides: A Diastereoselective Synthesis of 1,2-Dihydronaphtho[2,1-b]furans and 2,3-Dihydrobenzofurans

inferred← citeshttps://doi.org/10.1021/jo402776uopenalex-snapshot

KOtBu-Mediated Synthesis of Dimethylisoindolin-1-ones and Dimethyl-5-phenylisoindolin-1-ones: Selective C–C Coupling of an Unreactive Tertiary sp3 C–H Bond

inferred← citeshttps://doi.org/10.1021/ml300064vopenalex-snapshot

Low Doses of Allyphenyline and Cyclomethyline, Effective against Morphine Dependence, Elicit an Antidepressant-like Effect

inferred← citeshttps://doi.org/10.1021/ol203043hopenalex-snapshot

Regioselective Pd-Catalyzed Aerobic Aza-Wacker Cyclization for Preparation of Isoindolinones and Isoquinolin-1(2H)-ones

inferred← citeshttps://doi.org/10.1021/om800390wopenalex-snapshot

Tuning the Reactivity of Palladium Carbenes Derived from Diphenylketene

inferred← citeshttps://doi.org/10.1038/s41467-024-45697-yopenalex-snapshot

Zirconium and hafnium catalyzed C–C single bond hydroboration

inferred← citeshttps://doi.org/10.1039/b614710kopenalex-snapshot

Transition metals in organic synthesis: cross-coupling, C–H activation processes and cyclisation strategies

inferred← citeshttps://doi.org/10.1039/c1sc00458aopenalex-snapshot

Palladium(0)-catalyzed cyclopropane C–H bond functionalization: synthesis of quinoline and tetrahydroquinoline derivatives

inferred← citeshttps://doi.org/10.1039/c7qo00846eopenalex-snapshot

1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans

inferred← citeshttps://doi.org/10.1039/c7sc00071eopenalex-snapshot

Rh-catalyzed regiodivergent hydrosilylation of acyl aminocyclopropanes controlled by monophosphine ligands

inferred← citeshttps://doi.org/10.1039/c8sc01537fopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1039/c9ra09987eopenalex-snapshot

Dihydronaphthofurans: synthetic strategies and applications

inferred← citeshttps://doi.org/10.1039/d2cc01917eopenalex-snapshot

Access to hexahydroazepinone heterocycles via palladium-catalysed C(sp 3 )–H alkenylation/ring-opening of cyclopropanes

inferred← citeshttps://doi.org/10.1055/s-0030-1260087openalex-snapshot

Palladium-Catalyzed Ligand-Directed Oxidative Functionalization of Cyclopropanes

inferred← citeshttps://doi.org/10.1080/00304940903507788openalex-snapshot

Arylcyclopropanes: Properties, Synthesis and Use in Medicinal Chemistry

inferred← citeshttps://doi.org/10.1080/00397911.2014.887732openalex-snapshot

Utility of 2-Methoxy-1-naphthaldehyde in Heterocyclic Synthesis

inferred← citeshttps://doi.org/10.1080/00397911.2015.1017052openalex-snapshot

One-Pot Green Synthesis of Novel Polysubstituted 1,2-Dihydronaphtho[2,1-b]furans

inferred← citeshttps://doi.org/10.11648/j.ijsts.20231106.14openalex-snapshot

Further Insights into the Exhaustive Grignard Tetramethylation of N-benzylphthalimide

inferred← citeshttps://doi.org/10.3390/molecules27103147openalex-snapshot

An Easy Access to Furan-Fused Polyheterocyclic Systems

inferred← citeshttps://doi.org/10.3987/com-07-11304openalex-snapshot

Synthesis of 2,4-Disubstituted Isoquinolin-1(2H)-ones Based on Reactions of a-Substituted 2-Lithio-b-methoxystyrenes with Isocyanates

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.