On the public citation graph

Discovery, Biological Evaluation, and Structure–Activity and −Selectivity Relationships of 6′-Substituted ( E )-2-(Benzofuran-3(2 H )-ylidene)- N -methylacetamides, a Novel Class of Potent and Selective Monoamine Oxidase Inhibitors

https://doi.org/10.1021/jm4000769
0 signed · 120 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1001/archneur.62.2.241openalex-snapshot
A Randomized Placebo-Controlled Trial of Rasagiline in Levodopa-Treated Patients With Parkinson Disease and Motor Fluctuations
inferredcites →https://doi.org/10.1002/cber.188401701248openalex-snapshot
Neue Bildungsweise der Cumarine. Synthese des Daphnetins. I
inferredcites →https://doi.org/10.1002/prot.10465openalex-snapshot
Improved protein–ligand docking using GOLD
inferredcites →https://doi.org/10.1007/bf00500765openalex-snapshot
The deamination of dopamine by human brain monoamine oxidase
inferredcites →https://doi.org/10.1007/bf00978365openalex-snapshot
Monoamine oxidase inhibitors and the cheese effect
inferredcites →https://doi.org/10.1007/bf02231196openalex-snapshot
Hepatitis associated with iproniazid (Marsilid®)
inferredcites →https://doi.org/10.1007/s10822-008-9169-8openalex-snapshot
Evaluating docking programs: keeping the playing field level
inferredcites →https://doi.org/10.1007/s11064-009-9929-4openalex-snapshot
Altered Platelet Monoamine Oxidase-B Activity in Idiopathic Parkinson’s Disease
inferredcites →https://doi.org/10.1016/0306-4522(94)90311-5openalex-snapshot
Increased monoamine oxidase b activity in plaque-associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography
inferredcites →https://doi.org/10.1016/j.bmc.2008.09.072openalex-snapshot
Synthesis, structure–activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B
inferredcites →https://doi.org/10.1016/j.bmc.2010.06.007openalex-snapshot
Investigations on the 2-thiazolylhydrazyne scaffold: Synthesis and molecular modeling of selective human monoamine oxidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2010.11.028openalex-snapshot
Inhibition of monoamine oxidase by selected C5- and C6-substituted isatin analogues
inferredcites →https://doi.org/10.1016/j.bmc.2012.05.048openalex-snapshot
Inhibition of monoamine oxidase by 8-phenoxymethylcaffeine derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2009.07.039openalex-snapshot
Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors
inferredcites →https://doi.org/10.1016/j.cellsig.2012.01.008openalex-snapshot
Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling
inferredcites →https://doi.org/10.1016/j.ejmech.2010.07.005openalex-snapshot
Inhibition of monoamine oxidase by indole and benzofuran derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2012.01.037openalex-snapshot
Inhibition of monoamine oxidase by selected C6-substituted chromone derivatives
inferredcites →https://doi.org/10.1016/j.tips.2004.11.007openalex-snapshot
Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders
inferredcites →https://doi.org/10.1016/s0024-3205(01)01178-xopenalex-snapshot
Inhibition of brain monoamine oxidase activity by the generation of hydroxyl radicals Potential implications in relation to oxidative stress
inferredcites →https://doi.org/10.1016/s0024-3205(97)00114-8openalex-snapshot
Inhibition of brain monoamine oxidase by adducts of 1,2,3,4-tetrahydroisoquinoline with components of cigarette smoke
inferredcites →https://doi.org/10.1016/s0161-813x(03)00097-4openalex-snapshot
Clinical Pharmacology of MAO Inhibitors: Safety and Future
inferredcites →https://doi.org/10.1016/s0161-813x(03)00102-5openalex-snapshot
(−)-Deprenyl, A Selective MAO-B Inhibitor, with Apoptotic and Anti-apoptotic Properties
inferredcites →https://doi.org/10.1021/ci800298zopenalex-snapshot
Empirical Scoring Functions for Advanced Protein−Ligand Docking with PLANTS
inferredcites →https://doi.org/10.1021/jm00019a018openalex-snapshot
Inhibition of Monoamine Oxidase-B by 5H-Indeno[1,2-c]pyridazines: Biological Activities, Quantitative Structure-Activity Relationships (QSARs) and 3D-QSARs
inferredcites →https://doi.org/10.1021/jm001028oopenalex-snapshot
Inhibition of Monoamine Oxidases by Functionalized Coumarin Derivatives: Biological Activities, QSARs, and 3D-QSARs
inferredcites →https://doi.org/10.1021/jm020120copenalex-snapshot
Novel Dual Inhibitors of AChE and MAO Derived from Hydroxy Aminoindan and Phenethylamine as Potential Treatment for Alzheimer's Disease
inferredcites →https://doi.org/10.1021/jm050543popenalex-snapshot
Modeling Water Molecules in Protein−Ligand Docking Using GOLD
inferredcites →https://doi.org/10.1021/jm060183lopenalex-snapshot
Structural Insights into Monoamine Oxidase Inhibitory Potency and Selectivity of 7-Substituted Coumarins from Ligand- and Target-Based Approaches
inferredcites →https://doi.org/10.1021/jm070677yopenalex-snapshot
Structures of Human Monoamine Oxidase B Complexes with Selective Noncovalent Inhibitors: Safinamide and Coumarin Analogs
inferredcites →https://doi.org/10.1021/jm070725eopenalex-snapshot
Solid-Phase Synthesis and Insights into Structure−Activity Relationships of Safinamide Analogues as Potent and Selective Inhibitors of Type B Monoamine Oxidase
inferredcites →https://doi.org/10.1021/jm070728ropenalex-snapshot
Synthesis and Monoamine Oxidase Inhibitory Activity of New Pyridazine-, Pyrimidine- and 1,2,4-Triazine-Containing Tricyclic Derivatives
inferredcites →https://doi.org/10.1021/jm2002876openalex-snapshot
3-Acetyl-2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoles: A New Scaffold for the Selective Inhibition of Monoamine Oxidase B
inferredcites →https://doi.org/10.1021/jm200716yopenalex-snapshot
Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors
inferredcites →https://doi.org/10.1021/jm801496uopenalex-snapshot
Synthesis, Molecular Modeling, and Selective Inhibitory Activity against Human Monoamine Oxidases of 3-Carboxamido-7-Substituted Coumarins
inferredcites →https://doi.org/10.1021/jm9010127openalex-snapshot
Discovery of a Novel Class of Potent Coumarin Monoamine Oxidase B Inhibitors: Development and Biopharmacological Profiling of 7-[(3-Chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one Methanesulfonate (NW-1772) as a Highly Potent, Selective, Reversible, and Orally Active Monoamine Oxidase B…
inferredcites →https://doi.org/10.1038/nature05292openalex-snapshot
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
inferredcites →https://doi.org/10.1038/nrn1537openalex-snapshot
Iron, brain ageing and neurodegenerative disorders
inferredcites →https://doi.org/10.1038/nrn1883openalex-snapshot
The therapeutic potential of monoamine oxidase inhibitors
inferredcites →https://doi.org/10.1038/nsb732openalex-snapshot
Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders
inferredcites →https://doi.org/10.1055/s-1979-28602openalex-snapshot
Hexamethylenetetramine, A Versatile Reagent in Organic Synthesis
inferredcites →https://doi.org/10.1073/pnas.0505975102openalex-snapshot
Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B
inferredcites →https://doi.org/10.1073/pnas.0710626105openalex-snapshot
Structure of human monoamine oxidase A at 2.2-Å resolution: The control of opening the entry for substrates/inhibitors
inferredcites →https://doi.org/10.1073/pnas.1633804100openalex-snapshot
Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures
inferredcites →https://doi.org/10.1097/00131746-200407000-00005openalex-snapshot
The Role of Monoamine Oxidase Inhibitors in Current Psychiatric Practice
inferredcites →https://doi.org/10.1111/j.1471-4159.1990.tb03121.xopenalex-snapshot
Tissue Distribution of Human Monoamine Oxidase A and B mRNA
inferredcites →https://doi.org/10.1126/science.3099392openalex-snapshot
Mapping Human Brain Monoamine Oxidase A and B with11C-Labeled Suicide Inactivators and PET
inferredcites →https://doi.org/10.1136/bmj.2.5104.1068openalex-snapshot
Jaundice Associated with Administration of Iproniazid
inferredcites →https://doi.org/10.1146/annurev.neuro.22.1.197openalex-snapshot
MONOAMINE OXIDASE: From Genes to Behavior
inferredcites →https://doi.org/10.1146/annurev.pa.36.040196.000503openalex-snapshot
Oxidative Stress in Neurodegenerative Diseases
inferredcites →https://doi.org/10.1586/14737175.5.6.811openalex-snapshot
Recent advances in Parkinson’s disease therapy: use of monoamine oxidase inhibitors
inferredcites →https://doi.org/10.2174/0929867043364784openalex-snapshot
Structure and Mechanism of Monoamine Oxidase
inferredcites →https://doi.org/10.2174/092986706776872907openalex-snapshot
Synthesis, Biological Evaluation and 3D-QSAR of 1,3,5-Trisubstituted-4,5- Dihydro-(1H)-Pyrazole Derivatives as Potent and Highly Selective Monoamine Oxidase A Inhibitors
inferredcites →https://doi.org/10.2174/092986711797379302openalex-snapshot
Targeting Monoamine Oxidases with Multipotent Ligands: An Emerging Strategy in the Search of New Drugs Against Neurodegenerative Diseases
inferredcites →https://doi.org/10.2174/138161210793176527openalex-snapshot
Monoamine Oxidase Inhibitors as Neuroprotective Agents in Age-Dependent Neurodegenerative Disorders
inferredcites →https://doi.org/10.2174/138955712802762301openalex-snapshot
Discovery of MAO-B Inhibitors - Present Status and Future Directions Part I: Oxygen Heterocycles and Analogs
inferredcites →https://doi.org/10.3949/ccjm.77a.09103openalex-snapshot
MAO inhibitors: Risks, benefits, and lore
inferredcites →https://doi.org/10.3987/com-94-6996openalex-snapshot
A Convenient Synthesis of Benzofuran-3-acetic Acids
inferredcites →https://doi.org/10.7270/q2nk3f9xopenalex-snapshot
BindingDB Entry 50032703: Synthesis and evaluation ofß-carboline derivatives as potential monoamine oxidase inhibitors.

What points at this work

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

inferred← citeshttps://doi.org/10.3897/pharmacia.73.e206275zenodo-depositor-declared
Exploring benzofuran derivatives as selective MAO-B inhibitors: a multilayered in silico study
inferred← citeshttps://doi.org/10.1002/0471264229.os096.07openalex-snapshot
Discussion Addendum for: Convenient Preparation of 3‐Ethoxycarbonyl Benzofurans from Salicylaldehydes and Ethyl Diazoacetate
inferred← citeshttps://doi.org/10.1002/ajoc.202200554openalex-snapshot
An Expedient Iodine‐Catalyzed Synthesis of Unsymmetrical Thiosulfonates by Sulfonylation of Thiols using Sulfonyl hydrazides in the Presence of Oxone
inferred← citeshttps://doi.org/10.1002/ange.201503654openalex-snapshot
Catalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase B
inferred← citeshttps://doi.org/10.1002/anie.201503654openalex-snapshot
Catalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase B
inferred← citeshttps://doi.org/10.1002/ardp.202200084openalex-snapshot
Revealing the role of the benzyloxy pharmacophore in the design of a new class of monoamine oxidase‐B inhibitors
inferred← citeshttps://doi.org/10.1002/cbdv.202200140openalex-snapshot
Synthesis, Biological Activity and Molecular Docking Studies of Novel Sulfonate Derivatives Bearing Salicylaldehyde
inferred← citeshttps://doi.org/10.1002/cctc.201400091openalex-snapshot
Palladium(II)/Polyoxometalate‐Catalyzed Direct Alkenylation of Benzofurans under Atmospheric Dioxygen
inferred← citeshttps://doi.org/10.1002/cmdc.201700282openalex-snapshot
Discovery of Potent Dual Binding Site Acetylcholinesterase Inhibitors via Homo‐ and Heterodimerization of Coumarin‐Based Moieties
inferred← citeshttps://doi.org/10.1002/ejoc.70600openalex-snapshot
Electrochemical Three‐Component Synthesis of Heteroaryl Sulfonates
inferred← citeshttps://doi.org/10.1002/jbt.22651openalex-snapshot
Identification of 7,8‐dihydroxy‐3‐phenylcoumarin as a reversible monoamine oxidase enzyme inhibitor
inferred← citeshttps://doi.org/10.1002/open.202400516openalex-snapshot
Design, Synthesis, Biological Evaluation, and In Silico Study of Tetrahydropyridines as Prospective Monoamine Oxidase Inhibitors
inferred← citeshttps://doi.org/10.1002/slct.202202440openalex-snapshot
Functionalization of Sulfonic Acid to Sulfonic Ester Using Diazo Compound under Mild Reaction Conditions in the Absence of Additives
inferred← citeshttps://doi.org/10.1007/s10593-018-2281-3openalex-snapshot
4-Hydroxycoumarins as Michael donors in asymmetric routes to polycyclic coumarins (microreview)
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106224openalex-snapshot
Novel AP2238-clorgiline hybrids as multi-target agents for the treatment of Alzheimer's disease: Design, synthesis, and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.04.012openalex-snapshot
Synthesis and evaluation of 4-hydroxyl aurone derivatives as multifunctional agents for the treatment of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.03.060openalex-snapshot
Discovery, synthesis, biological evaluation and molecular docking study of (R)-5-methylmellein and its analogs as selective monoamine oxidase A inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.09.034openalex-snapshot
Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.10.021openalex-snapshot
Discovery of new 7-substituted-4-imidazolylmethyl coumarins and 4′-substituted-2-imidazolyl acetophenones open analogues as potent and selective inhibitors of steroid-11β-hydroxylase
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.10.029openalex-snapshot
In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.10.085openalex-snapshot
Biological and medicinal significance of benzofuran
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.10.016openalex-snapshot
Investigating alkyl nitrates as nitric oxide releasing precursors of multitarget acetylcholinesterase-monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117580openalex-snapshot
2-(Phenylamino)-7,8-dihydroquinazolin-5(6H)-one, a promising scaffold for MAO-B inhibitors with potential GSK3β targeting
inferred← citeshttps://doi.org/10.1016/j.ejps.2017.02.008openalex-snapshot
A rational approach to elucidate human monoamine oxidase molecular selectivity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.141350openalex-snapshot
Synthesis, design, and cholinesterase inhibitory activity of novel 1,2,4-triazole Schiff bases: A combined experimental and computational approach
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.03.055openalex-snapshot
Structural, computational and anticancer activity studies of D-seco-17-mesyloxy androstane derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133444openalex-snapshot
Synthesis, molecular modeling, 3D-QSAR and biological evaluation studies of new benzimidazole derivatives as potential MAO-A and MAO-B inhibitors
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.02.068openalex-snapshot
A microwave-assisted multicomponent protocol for the synthesis of benzofuran-2-carboxamides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151660openalex-snapshot
NFSI/KF mediated mild and chemoselective interconversion of aryl TBDMS ethers to their benzene sulfonate
inferred← citeshttps://doi.org/10.1016/j.virusres.2024.199432openalex-snapshot
Identification of new benzofuran derivatives as STING agonists with broad-spectrum antiviral activity
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00599openalex-snapshot
Structure-Based Design and Optimization of Multitarget-Directed 2H-Chromen-2-one Derivatives as Potent Inhibitors of Monoamine Oxidase B and Cholinesterases
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b00562openalex-snapshot
Exploring Basic Tail Modifications of Coumarin-Based Dual Acetylcholinesterase-Monoamine Oxidase B Inhibitors: Identification of Water-Soluble, Brain-Permeant Neuroprotective Multitarget Agents
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00260openalex-snapshot
Practical Electro-Oxidative Sulfonylation of Phenols with Sodium Arenesulfinates Generating Arylsulfonate Esters
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01151openalex-snapshot
Metal-Free Oxidative Formation of Aryl Esters by Catalytic Coupling of Acyl and Sulfonyl Chlorides with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01278openalex-snapshot
Palladium-Catalyzed C–H Bond Functionalization Reactions Using Phosphate/Sulfonate Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1021/acsomega.2c04653openalex-snapshot
Synthesis of 7-Aminocoumarins from 7-Hydroxycoumarins via Amide Smiles Rearrangement
inferred← citeshttps://doi.org/10.1021/acsomega.3c07703openalex-snapshot
Design, Synthesis, and Biological Effect Studies of Novel Benzofuran–Thiazolylhydrazone Derivatives as Monoamine Oxidase Inhibitors
inferred← citeshttps://doi.org/10.1038/s41598-022-26929-xopenalex-snapshot
Introduction of benzyloxy pharmacophore into aryl/heteroaryl chalcone motifs as a new class of monoamine oxidase B inhibitors
inferred← citeshttps://doi.org/10.1039/c5ra00724kopenalex-snapshot
Iodine-induced synthesis of sulfonate esters from sodium sulfinates and phenols under mild conditions
inferred← citeshttps://doi.org/10.1039/c6ra00302hopenalex-snapshot
Recent developments on the structure–activity relationship studies of MAO inhibitors and their role in different neurological disorders
inferred← citeshttps://doi.org/10.1039/c7md00311kopenalex-snapshot
MAO inhibitory activity of bromo-2-phenylbenzofurans: synthesis, in vitro study, and docking calculations
inferred← citeshttps://doi.org/10.1039/c7ob01337jopenalex-snapshot
Synthesis of 1H-indole-3-sulfonates via palladium-catalyzed tandem reactions of 2-alkynyl arylazides with sulfonic acids
inferred← citeshttps://doi.org/10.1039/c7ra09053fopenalex-snapshot
Iodobenzene-catalyzed synthesis of aryl sulfonate esters from aminoquinolines via remote radical C–O cross-coupling
inferred← citeshttps://doi.org/10.1039/d1nj05644aopenalex-snapshot
Synthesis of 2-styryl-quinazoline and 3-styryl-quinoxaline based sulfonate esters via sp 3 C–H activation and their evaluation for α-glucosidase inhibition
inferred← citeshttps://doi.org/10.1039/d2ra02656bopenalex-snapshot
Visible-light-induced one-pot synthesis of sulfonic esters via multicomponent reaction of arylazo sulfones and alcohols
inferred← citeshttps://doi.org/10.1039/d3ra02067copenalex-snapshot
Visible-light-driven reactions for the synthesis of sulfur dioxide-inserted compounds: generation of S–F, S–O, and S–N bonds
inferred← citeshttps://doi.org/10.1055/s-0039-1690820openalex-snapshot
Recent Advances in Synthetic Strategies to 2,3-Dihydrobenzofurans
inferred← citeshttps://doi.org/10.1080/00397911.2020.1794657openalex-snapshot
A simple method for the synthesis of sulfonic esters
inferred← citeshttps://doi.org/10.1107/s2053229618008355openalex-snapshot
A comparative experimental and theoretical investigation of hydrogen-bond, halogen-bond and π–π interactions in the solid-state supramolecular assembly of 2- and 4-formylphenyl arylsulfonates
inferred← citeshttps://doi.org/10.1107/s2414314617002000openalex-snapshot
2-(5-Methyl-1-benzofuran-3-yl)-N-(2-phenylethyl)acetamide
inferred← citeshttps://doi.org/10.1201/9781315368863-12openalex-snapshot
High-Order Perturbation Theory Models of Drug-Target Interactomes for Proteins Expressed on Networks of Hippocampus Brain Region of Alzheimer Disease Patients
inferred← citeshttps://doi.org/10.1248/bpb.b20-00093openalex-snapshot
Antidepressant Activity of Euparin: Involvement of Monoaminergic Neurotransmitters and SAT1/NMDAR2B/BDNF Signal Pathway
inferred← citeshttps://doi.org/10.2174/0929867325666180514110824openalex-snapshot
Advances in the Treatment of Explicit Water Molecules in Docking and Binding Free Energy Calculations
inferred← citeshttps://doi.org/10.2174/1386207321666180313130314openalex-snapshot
Docking of Natural Products against Neurodegenerative Diseases: General Concepts
inferred← citeshttps://doi.org/10.2174/1568026615666150610143510openalex-snapshot
Computer Aided Drug Design Studies in the Discovery of Secondary Metabolites Targeted Against Age-Related Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3389/fchem.2022.1002547openalex-snapshot
A twenty-year journey exploring coumarin-based derivatives as bioactive molecules
inferred← citeshttps://doi.org/10.3390/molecules21030362openalex-snapshot
Searching for Multi-Targeting Neurotherapeutics against Alzheimer’s: Discovery of Potent AChE-MAO B Inhibitors through the Decoration of the 2H-Chromen-2-one Structural Motif
inferred← citeshttps://doi.org/10.3390/molecules23020250openalex-snapshot
Coumarin: A Natural, Privileged and Versatile Scaffold for Bioactive Compounds
inferred← citeshttps://doi.org/10.3390/molecules24244507openalex-snapshot
Chasing ChEs-MAO B Multi-Targeting 4-Aminomethyl-7-Benzyloxy-2H-Chromen-2-ones
inferred← citeshttps://doi.org/10.3390/molecules26195895openalex-snapshot
Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Chlorobenzenesulfonates
inferred← citeshttps://doi.org/10.3390/ph18101526openalex-snapshot
Monoamine Oxidase Inhibitors in Drug Discovery Against Parkinson’s Disease: An Update
inferred← citeshttps://doi.org/10.6023/cjoc202107060openalex-snapshot
Electrochemical Synthesis of Aryl Sulfonates from Sodium Sulfinates and Phenols under Metal-Free Conditions
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.