On the public citation graph

Rhenium-Catalyzed Regioselective Alkylation of Phenols

0 signed · 129 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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.200606068openalex-snapshot

An Effective Bismuth‐Catalyzed Benzylation of Arenes and Heteroarenes

inferredcites →https://doi.org/10.1002/anie.200461559openalex-snapshot

Rhenium( I )‐Catalyzed Intramolecular Geminal Carbofunctionalization of Alkynes: Tandem Cyclization of ω‐Acetylenic Dienol Silyl Ethers

inferredcites →https://doi.org/10.1002/anie.200803350openalex-snapshot

Rhenium‐Catalyzed Synthesis of Stereodefined Cyclopentenes from β‐Ketoesters and Aliphatic Allenes

inferredcites →https://doi.org/10.1016/j.catcom.2007.09.007openalex-snapshot

Catalytic performance of Preyssler heteropolyacid, [NaP5W30O110]14− in liquid phase alkylation of phenol with 1-octene

inferredcites →https://doi.org/10.1016/j.jorganchem.2004.08.018openalex-snapshot

Methyltrioxorhenium and its applications in olefin oxidation, metathesis and aldehyde olefination

inferredcites →https://doi.org/10.1016/j.jorganchem.2005.05.011openalex-snapshot

Intramolecular hydroamination of 6-aminohex-1-yne catalyzed by Lewis acidic rhenium(I) carbonyl complexes

inferredcites →https://doi.org/10.1016/j.tetlet.2007.07.178openalex-snapshot

Highly efficient iodine-catalyzed hydroarylation of arenes with styrenes

inferredcites →https://doi.org/10.1021/cr60058a002openalex-snapshot

The Friedel-Crafts Syntheses.

inferredcites →https://doi.org/10.1021/ja00089a054openalex-snapshot

Stereoselective Olefin Insertion Reactions of Chiral (EBI)Zr(.eta.2-pyrid-2-yl)+ and (EBTHI)Zr(.eta.2-pyrid-2-yl)+ Complexes

inferredcites →https://doi.org/10.1021/ja0009830openalex-snapshot

Anti-Markovnikov Olefin Arylation Catalyzed by an Iridium Complex

inferredcites →https://doi.org/10.1021/ja00184a081openalex-snapshot

Zirconium-catalyzed coupling of propene and .alpha.-picoline

inferredcites →https://doi.org/10.1021/ja00270a036openalex-snapshot

Catalytic carbon-carbon bond formation via ortho-metalated complexes

inferredcites →https://doi.org/10.1021/ja039124copenalex-snapshot

Rhenium-Catalyzed Coupling of Propargyl Alcohols and Allyl Silanes

inferredcites →https://doi.org/10.1021/ja050831aopenalex-snapshot

Enantioselective Reduction of Imines Catalyzed by a Rhenium(V)−Oxo Complex

inferredcites →https://doi.org/10.1021/ja0528174openalex-snapshot

Rhenium-Catalyzed Formation of Indene Frameworks via C−H Bond Activation: [3+2] Annulation of Aromatic Aldimines and Acetylenes

inferredcites →https://doi.org/10.1021/ja064022iopenalex-snapshot

Efficient Catalytic Insertion of Acetylenes into a Carbon−Carbon Single Bond of Nonstrained Cyclic Compounds under Mild Conditions

inferredcites →https://doi.org/10.1021/ja065643eopenalex-snapshot

Rhenium-Catalyzed Insertion of Aldehyde into a C−H Bond: Synthesis of Isobenzofuran Derivatives

inferredcites →https://doi.org/10.1021/ja805921fopenalex-snapshot

Synthesis of Cp−Re Complexes via Olefinic C−H Activation and Successive Formation of Cyclopentadienes

inferredcites →https://doi.org/10.1021/jo061221bopenalex-snapshot

Ag(I)-Catalyzed Sequential C−C and C−O Bond Formations between Phenols and Dienes with Atom Economy

inferredcites →https://doi.org/10.1021/ol0515208openalex-snapshot

Rhenium-Catalyzed Insertion of Terminal Acetylenes into a C−H Bond of Active Methylene Compounds

inferredcites →https://doi.org/10.1021/ol0607692openalex-snapshot

Highly Efficient Gold-Catalyzed Atom-Economical Annulation of Phenols with Dienes

inferredcites →https://doi.org/10.1021/ol702564eopenalex-snapshot

Rhenium-Catalyzed Hydroamidation of Unactivated Terminal Alkynes: Synthesis of (E)-Enamides

inferredcites →https://doi.org/10.1039/a604598gopenalex-snapshot

Acidity effect in the regiochemical control of the alkylation of phenol with alkenes

inferredcites →https://doi.org/10.1039/b208680hopenalex-snapshot

Novel bis-acac-O,O–Ir( iii ) catalyst for anti-Markovnikov, hydroarylation of olefins operates by arene CH activation

inferredcites →https://doi.org/10.1039/b211672copenalex-snapshot

Addition of the ortho-C–H bonds of phenol across an olefin catalysed by a chiral iridium(i) diphosphine complex

inferredcites →https://doi.org/10.1039/b610038dopenalex-snapshot

Halide-free ethylation of phenol by multifunctional catalysis using phosphinite ligands

inferredcites →https://doi.org/10.1246/bcsj.73.2779openalex-snapshot

Rhenium Complexes-Catalyzed Alkylation of Arenes with Alkyl Halides

inferredcites →https://doi.org/10.1246/cl.2006.1376openalex-snapshot

Rhenium-catalyzed Addition of Trimethylsilylacetylene to Aldimines

inferredcites →https://doi.org/10.1246/cl.2007.1162openalex-snapshot

Rhenium-catalyzed [2+2] Cycloadditions of Norbornenes with Internal and Terminal Acetylenes

inferredcites →https://doi.org/10.1246/cl.2008.878openalex-snapshot

Rhenium-catalyzed Coupling of 2-Propynyl Alcohols and Several Nucleophiles via Dehydration

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.4669910openalex-extracted

inferred← citeshttps://doi.org/10.1002/047084289x.rd002.pub2openalex-snapshot

Decacarbonyldirhenium

inferred← citeshttps://doi.org/10.1002/0471264180.or100.10openalex-snapshot

ortho ‐Directed CH Alkylation of Substituted Benzenes

inferred← citeshttps://doi.org/10.1002/0471264229.os094.20openalex-snapshot

Rhenium‐Catalyzed ortho ‐Alkylation of Phenols

inferred← citeshttps://doi.org/10.1002/9780471264194.fos11773openalex-snapshot

Rhenium Carbonyl Clusters

inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-003openalex-snapshot

Friedel‐Crafts and Related Alkylation Reactions

inferred← citeshttps://doi.org/10.1002/9781118998939.ch10openalex-snapshot

Homoleptic Metal Carbonyls in Organic Transformation

inferred← citeshttps://doi.org/10.1002/9781119972471.ch11openalex-snapshot

Addition Reactions: Polar Addition

inferred← citeshttps://doi.org/10.1002/9781119972471.ch6openalex-snapshot

Electrophilic Aromatic Substitution

inferred← citeshttps://doi.org/10.1002/adsc.201000476openalex-snapshot

The First Decarbonylative Coupling of Aldehydes and Norbornenes Catalyzed by Rhodium

inferred← citeshttps://doi.org/10.1002/ange.201200809openalex-snapshot

Regio‐ and Stereocontrolled Introduction of Secondary Alkyl Groups to Electron‐Deficient Arenes through Copper‐Catalyzed Allylic Alkylation

inferred← citeshttps://doi.org/10.1002/ange.201206233openalex-snapshot

Regioselective CH Alkylation of Anisoles with Olefins Catalyzed by Cationic Half‐Sandwich Rare Earth Alkyl Complexes

inferred← citeshttps://doi.org/10.1002/ange.201206611openalex-snapshot

FeCl3‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N‐Acetyl Indoles for the Synthesis of Benzofuroindolines

inferred← citeshttps://doi.org/10.1002/ange.201209312openalex-snapshot

Copper‐Catalyzed Direct Secondary and Tertiary CH Alkylation of Azoles through a Heteroarene–Amine–Aldehyde/Ketone Coupling Reaction

inferred← citeshttps://doi.org/10.1002/ange.201806629openalex-snapshot

Jenseits von Friedel und Crafts: dirigierte Alkylierung von C‐H‐Bindungen in Arenen

inferred← citeshttps://doi.org/10.1002/ange.201811729openalex-snapshot

Chemoselective Borane‐Catalyzed Hydroarylation of 1,3‐Dienes with Phenols

inferred← citeshttps://doi.org/10.1002/anie.201200809openalex-snapshot

Regio‐ and Stereocontrolled Introduction of Secondary Alkyl Groups to Electron‐Deficient Arenes through Copper‐Catalyzed Allylic Alkylation

inferred← citeshttps://doi.org/10.1002/anie.201206233openalex-snapshot

Regioselective CH Alkylation of Anisoles with Olefins Catalyzed by Cationic Half‐Sandwich Rare Earth Alkyl Complexes

inferred← citeshttps://doi.org/10.1002/anie.201206611openalex-snapshot

FeCl3‐Mediated Friedel–Crafts Hydroarylation with Electrophilic N‐Acetyl Indoles for the Synthesis of Benzofuroindolines

inferred← citeshttps://doi.org/10.1002/anie.201209312openalex-snapshot

Copper‐Catalyzed Direct Secondary and Tertiary CH Alkylation of Azoles through a Heteroarene–Amine–Aldehyde/Ketone Coupling Reaction

inferred← citeshttps://doi.org/10.1002/anie.201806629openalex-snapshot

Beyond Friedel and Crafts: Directed Alkylation of C−H Bonds in Arenes

inferred← citeshttps://doi.org/10.1002/anie.201811729openalex-snapshot

Chemoselective Borane‐Catalyzed Hydroarylation of 1,3‐Dienes with Phenols

inferred← citeshttps://doi.org/10.1002/asia.201400135openalex-snapshot

Alkene Isomerization–Hydroarylation Tandem Catalysis: Indole C2‐Alkylation with Aryl‐Substituted Alkenes Leading to 1,1‐Diarylalkanes

inferred← citeshttps://doi.org/10.1002/chem.201400284openalex-snapshot

Regioselective Hydroarylation Reactions of C3 Electrophilic N‐Acetylindoles Activated by FeCl3: An Entry to 3‐(Hetero)arylindolines

inferred← citeshttps://doi.org/10.1002/chem.201406562openalex-snapshot

Pd‐Catalyzed Csp2H Functionalization of Heteroarenes via Isocyanide Insertion: Concise Synthesis of Di‐(Hetero)Aryl Ketones and Di‐(Hetero)Aryl Alkylamines

inferred← citeshttps://doi.org/10.1002/chem.201700643openalex-snapshot

Electronic Control on Linear versus Branched Alkylation of 2‐/3‐Aroylbenzofurans with Acrylates: Combined DFT and Synthetic Studies

inferred← citeshttps://doi.org/10.1002/chem.201901914openalex-snapshot

Bioinspired Functional Catechol Derivatives through Simple Thiol Conjugate Addition

inferred← citeshttps://doi.org/10.1002/chem.201903910openalex-snapshot

Mechanistic Insights into Rhenium‐Catalyzed Regioselective C‐Alkenylation of Phenols with Internal Alkynes

inferred← citeshttps://doi.org/10.1002/chin.200951091openalex-snapshot

ChemInform Abstract: Rhenium‐Catalyzed Regioselective Alkylation of Phenols.

inferred← citeshttps://doi.org/10.1002/ejoc.201001180openalex-snapshot

Iron‐Catalyzed ortho‐Selective Functionalization of Phenols: A Straightforward Strategy towards the 2′‐Hydroxyphenyl‐1,2‐dione Skeleton

inferred← citeshttps://doi.org/10.1002/ejoc.201001398openalex-snapshot

Ring‐Opening Reaction of Vinylidenecyclopropanediesters Catalyzed by Re2(CO)10 or Yb(OTf)3

inferred← citeshttps://doi.org/10.1002/ejoc.201501211openalex-snapshot

Regioselective Multicomponent Synthesis of 2,4,6‐Trisubstituted Phenols from Fischer Alkynyl Carbene Complexes

inferred← citeshttps://doi.org/10.1002/ejoc.201900653openalex-snapshot

Gold‐Catalyzed Highly Chemo‐ and Regioselective C‐H Bond Functionalization of Phenols with Haloalkynes

inferred← citeshttps://doi.org/10.1007/s11243-016-0064-1openalex-snapshot

Synthesis and catalytic activity of monobridged bis(cyclopentadienyl)rhenium carbonyl complexes

inferred← citeshttps://doi.org/10.1007/s11243-016-0116-6openalex-snapshot

Synthesis and catalytic activity of rhenium carbonyl complexes containing alkyl-substituted tetramethylcyclopentadienyl ligands

inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00073-1openalex-snapshot

Complexes of Group 7 Metals with Metal-Carbon Sigma and Multiple Bonds

inferred← citeshttps://doi.org/10.1016/j.bse.2013.06.004openalex-snapshot

Chemical constituents from Metasequoia glyptostroboides Hu et Cheng

inferred← citeshttps://doi.org/10.1016/j.catcom.2021.106348openalex-snapshot

Facile preparation of Cu(II)-modified nitrogen-rich covalent organic polymer for cross-dehydrogenative ortho-aminomethylation of phenols

inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115351openalex-snapshot

Copper-catalyzed regioselective C−H alkylation of phenol derivatives with unactivated alkyl chlorides: Manifesting a Cu(I)/Cu(III) pathway

inferred← citeshttps://doi.org/10.1016/j.phytol.2012.07.006openalex-snapshot

A lanostane aldehyde from Momordica charantia

inferred← citeshttps://doi.org/10.1016/j.poly.2018.03.021openalex-snapshot

Synthesis and catalytic reactivity in Friedel–Crafts acylations of monobridged bis(cyclopentadienyl)molybdenum(I) carbonyl complexes

inferred← citeshttps://doi.org/10.1016/j.tet.2022.132757openalex-snapshot

Current Trends on C–C Bond Formation Through Regioselective Hydroarylation of Alkynes and Alkenes Using Metal Free Catalysts

inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.040openalex-snapshot

3D Nanoporous FeAl-KIT-5 with a cage type pore structure: a highly efficient and stable catalyst for hydroarylation of styrene and arylacetylenes

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.006openalex-snapshot

Hydroarylation of alkynes and alkenes through alumina-sulfuric acid catalyzed regioselective C C bond formation

inferred← citeshttps://doi.org/10.1021/acs.accounts.5b00414openalex-snapshot

Synthetic Transformations through Alkynoxy–Palladium Interactions and C–H Activation

inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00574openalex-snapshot

Transition-Metal-Catalyzed C–H Alkylation Using Alkenes

inferred← citeshttps://doi.org/10.1021/acs.joc.3c00639openalex-snapshot

Synthesis of 1-Aryltetralins via Re2O7/HReO4 Mediated Intramolecular Hydroarylations

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00860openalex-snapshot

Re2O7-Catalyzed Intermolecular Dehydrative Friedel–Crafts Reaction of Aliphatic Alcohols

inferred← citeshttps://doi.org/10.1021/acs.joc.9b03028openalex-snapshot

Phosphorous Acid-Catalyzed Alkylation of Phenols with Alkenes

inferred← citeshttps://doi.org/10.1021/acs.jpca.6b05735openalex-snapshot

DFT Calculations on the Mechanism of Transition-Metal-Catalyzed Reaction of Diazo Compounds with Phenols: O–H Insertion versus C–H Insertion

inferred← citeshttps://doi.org/10.1021/acs.jpca.7b06411openalex-snapshot

Origins of Protons in C–H Bond Insertion Products of Phenols: Proton-Self-Sufficient Function via Water Molecules

inferred← citeshttps://doi.org/10.1021/acs.oprd.0c00241openalex-snapshot

Development of a Green and Sustainable Manufacturing Process for Gefapixant Citrate (MK-7264) Part 2: Development of a Robust Process for Phenol Synthesis

inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00506openalex-snapshot

An Unusual Perpendicular Metallacycle Intermediate is the Origin of Branch Selectivity in the Rh(II)-Catalyzed C–H Alkylation of Aryl Sulfonamides with Vinylsilanes

inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00543openalex-snapshot

Mechanistic Study of a Re-Catalyzed Monoalkylation of Phenols

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01224openalex-snapshot

Rh(II)-Catalyzed C–H Alkylation of Benzylamines with Unactivated Alkenes: The Influence of Acid on Linear and Branch Selectivity

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01863openalex-snapshot

B(C6F5)3-Catalyzed Sequential Additions of Terminal Alkynes to para-Substituted Phenols: Selective Construction of Congested Phenol-Substituted Quaternary Carbons

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04322openalex-snapshot

Cu-Catalyzed Synthesis of Benzoxazole with Phenol and Cyclic Oxime

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03846openalex-snapshot

Re2O7/HReO4 Mediated Intramolecular Hydroacyloxylation of Unactivated Alkenes: A Dual Hydrogen-Bonding Effect

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/acscatal.0c05580openalex-snapshot

Unactivated Alkyl Halides in Transition-Metal-Catalyzed C–H Bond Alkylation

inferred← citeshttps://doi.org/10.1021/acscatal.2c01223openalex-snapshot

An Intermolecular Hydroarylation of Highly Deactivated Styrenes Catalyzed by Re2O7/HReO4 in Hexafluoroisopropanol

inferred← citeshttps://doi.org/10.1021/acscatal.4c00519openalex-snapshot

Iridium-Catalyzed Regiodivergent Atroposelective C–H Alkylation of Heterobiaryls with Alkenes

inferred← citeshttps://doi.org/10.1021/acscatal.5c00304openalex-snapshot

Late-Stage C–H Deuteration of (Hetero)Arenes via Deuterium-Bonding Enhanced Rhenium Catalysis

inferred← citeshttps://doi.org/10.1021/acscatal.5c02042openalex-snapshot

Ir-Catalyzed Regio- and Enantioselective C–H Addition to 1,1-Disubstituted Alkenes Enabled by the Directing Group: Construction of Acyclic Quaternary Stereocenters

inferred← citeshttps://doi.org/10.1021/cr100241uopenalex-snapshot

Organic Reactions Catalyzed by Rhenium Carbonyl Complexes

inferred← citeshttps://doi.org/10.1021/ja107187ropenalex-snapshot

Rhenium Hydride/Boron Lewis Acid Cocatalysis of Alkene Hydrogenations: Activities Comparable to Those of Precious Metal Systems

inferred← citeshttps://doi.org/10.1021/ja403759xopenalex-snapshot

Cobalt-Catalyzed Ortho Alkylation of Aromatic Imines with Primary and Secondary Alkyl Halides

inferred← citeshttps://doi.org/10.1021/jacs.7b08581openalex-snapshot

Branched-Selective Intermolecular Ketone α-Alkylation with Unactivated Alkenes via an Enamide Directing Strategy

inferred← citeshttps://doi.org/10.1021/jo5008465openalex-snapshot

Sulfoximine-Directed Ruthenium-Catalyzed ortho-C–H Alkenylation of (Hetero)Arenes: Synthesis of EP3 Receptor Antagonist Analogue

inferred← citeshttps://doi.org/10.1021/ol101627xopenalex-snapshot

Rhenium-Catalyzed Diastereoselective Synthesis of Aminoindanes via the Insertion of Allenes into a C−H Bond

inferred← citeshttps://doi.org/10.1021/om201187wopenalex-snapshot

Ethylene Reactions of a [ReH(η2-BH4)(NO)(PPh3)2] Complex: Reductive Elimination of Ethane and Oxidative Coupling to Butadiene

inferred← citeshttps://doi.org/10.1039/b918380aopenalex-snapshot

Manganese, technetium and rhenium

inferred← citeshttps://doi.org/10.1039/c0gc00330aopenalex-snapshot

Mechanism of efficient anti-Markovnikov olefin hydroarylation catalyzed by homogeneous Ir( iii ) complexes

inferred← citeshttps://doi.org/10.1039/c1dt10824gopenalex-snapshot

Rhenium ethoxy- and hydroxycarbene complexes with thiophene substituents

inferred← citeshttps://doi.org/10.1039/c1ra00401hopenalex-snapshot

Brønsted acidic ionic liquid: a simple, efficient and recyclable catalyst for regioselective alkylation of phenols and anti-Markovnikov addition of thiols to alkenes

inferred← citeshttps://doi.org/10.1039/c3ra46373gopenalex-snapshot

Oxidative ortho-amino-methylation of phenols via C–H and C–C bond cleavage

inferred← citeshttps://doi.org/10.1039/c4qo00149dopenalex-snapshot

Bi(OTf) 3 -catalysed synthesis of substituted indanes by a double hydroarylation of unactivated 1,3-dienes

inferred← citeshttps://doi.org/10.1039/c4qo00329bopenalex-snapshot

CO-enabled rhenium hydride catalyst for directed C(sp 2 )–H bond alkylation with olefins

inferred← citeshttps://doi.org/10.1039/c4qo00355aopenalex-snapshot

Cationic iridium-catalyzed C–H alkylation of 2-substituted pyridine N-oxides with acrylates

inferred← citeshttps://doi.org/10.1039/c5sc04319kopenalex-snapshot

Origins of unique gold-catalysed chemo- and site-selective C–H functionalization of phenols with diazo compounds

inferred← citeshttps://doi.org/10.1039/c9sc04308jopenalex-snapshot

Rh( ii )-catalyzed branch-selective C–H alkylation of aryl sulfonamides with vinylsilanes

inferred← citeshttps://doi.org/10.1039/d0ra09687copenalex-snapshot

Thiol-yne click reaction: an interesting way to derive thiol-provided catechols

inferred← citeshttps://doi.org/10.1039/d1nj02887aopenalex-snapshot

Silica–sulfuric acid and alumina–sulfuric acid: versatile supported Brønsted acid catalysts

inferred← citeshttps://doi.org/10.1039/d1ob00506eopenalex-snapshot

Transition-metal-catalyzed ortho -selective C–H functionalization reactions of free phenols

inferred← citeshttps://doi.org/10.1039/d1sc01731dopenalex-snapshot

Pd-catalyzed cross-electrophile Coupling/C–H alkylation reaction enabled by a mediator generated via C(sp 3 )–H activation

inferred← citeshttps://doi.org/10.1039/d4sc00687aopenalex-snapshot

Csp 2 –H functionalization of phenols: an effective access route to valuable materials via Csp 2 –C bond formation

inferred← citeshttps://doi.org/10.1039/d5qo01612fopenalex-snapshot

Rhenium-catalyzed stereoselective hydrocarboxylation of alkynes and olefins: late-stage NSAID drug's diversification

inferred← citeshttps://doi.org/10.1039/d6qo00268dopenalex-snapshot

Re( i )-catalyzed C–C and C–S bond formation via regioselective C(sp 2 )–H hydroalkylation and hydrothiolation

inferred← citeshttps://doi.org/10.1055/a-2382-3010openalex-snapshot

Iron(III) Triflate and γ-Cyclodextrin-Catalyzed Hydroarylation of Alkenes with 1-Naphthols and 2-Naphthols

inferred← citeshttps://doi.org/10.1055/sos-sd-131-00296openalex-snapshot

31.5.1.4.3 Synthesis of Phenols and Phenolates with Retention of the Functional Group (Update 2018)

inferred← citeshttps://doi.org/10.1055/sos-sd-217-00120openalex-snapshot

1.1.8 Metal-Catalyzed Alkylation Using Alkenes

inferred← citeshttps://doi.org/10.1080/14786419.2023.2256448openalex-snapshot

Anti-leishmanial and cytotoxic compounds isolated from marine sponge Hemimycale sp.

inferred← citeshttps://doi.org/10.1246/bcsj.20120015openalex-snapshot

Development of Novel and Highly Efficient Methods to Construct Carbon–Carbon Bonds Using Group 7 Transition-Metal Catalysts

inferred← citeshttps://doi.org/10.1246/bcsj.20150180openalex-snapshot

Alkynoxy-Directed C–H Functionalizations: Palladium(0)-Catalyzed Annulations of Alkynyl Aryl Ethers with Alkynes

inferred← citeshttps://doi.org/10.31635/ccschem.020.202000404openalex-snapshot

Chemoselective Dual Functionalization of Phenols via Relay Catalysis of Borane with Different Forms

inferred← citeshttps://doi.org/10.3390/molecules27061923openalex-snapshot

Iridium(I)-Catalyzed Isoindolinone-Directed Branched-Selective Aromatic C–H Alkylation with Simple Alkenes

inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.71.425openalex-snapshot

Transition Metal-Catalyzed Highly Efficient and Novel Transformations

inferred← citeshttps://doi.org/10.5283/epub.23463openalex-snapshot

Organic reactions of alcohols under hydrothermal conditions

inferred← citeshttps://doi.org/10.70675/ea73b65az1254z4f87z91f8z04658fa3d1c3openalex-snapshot

Formation de composés polycycliques par activation de doubles liaisons : approche catalytique intra et intermoléculaire de réactions de type Friedel-Crafts : applications au domaine des arômes et parfums

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.