On the public citation graph

4-( N,N -Dimethylamino)pyridine Hydrochloride as a Recyclable Catalyst for Acylation of Inert Alcohols: Substrate Scope and Reaction Mechanism

0 signed · 142 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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.200303072openalex-snapshot

Polymer‐Supported Lewis Bases for the Baylis–Hillman Reaction

inferredcites →https://doi.org/10.1002/anie.196909811openalex-snapshot

N,N‐Dimethyl‐4‐pyridinamine, a Very Effective Acylation Catalyst

inferredcites →https://doi.org/10.1002/anie.197805691openalex-snapshot

4‐Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)]

inferredcites →https://doi.org/10.1002/anie.200352289openalex-snapshot

Enhancing the Catalytic Activity of 4‐(Dialkylamino)pyridines by Conformational Fixation

inferredcites →https://doi.org/10.1002/anie.200461886openalex-snapshot

Nucleophile‐Catalyzed Asymmetric Acylations of Silyl Ketene Imines: Application to the Enantioselective Synthesis of Verapamil

inferredcites →https://doi.org/10.1002/anie.200501434openalex-snapshot

Catalytic Asymmetric Couplings of Ketenes with Aldehydes To Generate Enol Esters

inferredcites →https://doi.org/10.1002/anie.200605216openalex-snapshot

A Magnetic‐Nanoparticle‐Supported 4‐N,N‐Dialkylaminopyridine Catalyst: Excellent Reactivity Combined with Facile Catalyst Recovery and Recyclability

inferredcites →https://doi.org/10.1002/anie.200805805openalex-snapshot

Catalytic Asymmetric Cycloaddition of Ketenes and Nitroso Compounds: Enantioselective Synthesis of α‐Hydroxycarboxylic Acid Derivatives

inferredcites →https://doi.org/10.1002/chem.200500398openalex-snapshot

The DMAP‐Catalyzed Acetylation of Alcohols—A Mechanistic Study (DMAP=4‐(Dimethylamino)pyridine)

inferredcites →https://doi.org/10.1002/chem.200900532openalex-snapshot

The First Magnetic Nanoparticle‐Supported Chiral DMAP Analogue: Highly Enantioselective Acylation and Excellent Recyclability

inferredcites →https://doi.org/10.1002/chem.200901379openalex-snapshot

Structural Analyses of N‐Acetylated 4‐(Dimethylamino)pyridine (DMAP) Salts

inferredcites →https://doi.org/10.1002/chem.200902982openalex-snapshot

Fluorous 4‐N,N‐Dimethylaminopyridine (DMAP) Salts as Simple Recyclable Acylation Catalysts

inferredcites →https://doi.org/10.1002/chem.201103028openalex-snapshot

4‐(N,N‐Dimethylamino)pyridine‐Embedded Nanoporous Conjugated Polymer as a Highly Active Heterogeneous Organocatalyst

inferredcites →https://doi.org/10.1002/ejoc.201001507openalex-snapshot

Immobilized DMAP Derivatives Rivaling Homogeneous DMAP

inferredcites →https://doi.org/10.1002/pola.22681openalex-snapshot

Hairy particle‐supported 4‐N,N‐dialkylaminopyridine: An efficient and recyclable nucleophilic organocatalyst

inferredcites →https://doi.org/10.1016/j.bmcl.2011.06.038openalex-snapshot

Construction of a 19F-lectin biosensor for glycoprotein imaging by using affinity-guided DMAP chemistry

inferredcites →https://doi.org/10.1021/ja00367a025openalex-snapshot

Poly(ethylenimines) with alternative (alkylamino)pyridines as nucleophilic catalysts

inferredcites →https://doi.org/10.1021/ja027466xopenalex-snapshot

Enantioselective Addition of Amines to Ketenes Catalyzed by a Planar-Chiral Derivative of PPY: Possible Intervention of Chiral Brønsted-Acid Catalysis

inferredcites →https://doi.org/10.1021/ja0342852openalex-snapshot

Using Soluble Polymers in Latent Biphasic Systems

inferredcites →https://doi.org/10.1021/ja0524898openalex-snapshot

Dialkylaminopyridine-Functionalized Mesoporous Silica Nanosphere as an Efficient and Highly Stable Heterogeneous Nucleophilic Catalyst

inferredcites →https://doi.org/10.1021/ja063688+openalex-snapshot

Microencapsulated Linear Polymers: “Soluble” Heterogeneous Catalysts

inferredcites →https://doi.org/10.1021/ja0657859openalex-snapshot

Kinetic Resolutions of Indolines by a Nonenzymatic Acylation Catalyst

inferredcites →https://doi.org/10.1021/ja0717212openalex-snapshot

Functionalization of Single-Walled Carbon Nanotubes and Fullerenes via a Dimethyl Acetylenedicarboxylate−4-Dimethylaminopyridine Zwitterion Approach

inferredcites →https://doi.org/10.1021/ja075684qopenalex-snapshot

Target-Specific Chemical Acylation of Lectins by Ligand-Tethered DMAP Catalysts

inferredcites →https://doi.org/10.1021/ja075824wopenalex-snapshot

Widely Useful DMAP-Catalyzed Esterification under Auxiliary Base- and Solvent-Free Conditions

inferredcites →https://doi.org/10.1021/ja105337hopenalex-snapshot

Merging Nucleophilic and Hydrogen Bonding Catalysis: An Anion Binding Approach to the Kinetic Resolution of Propargylic Amines

inferredcites →https://doi.org/10.1021/ja204422ropenalex-snapshot

Chemical Cell-Surface Receptor Engineering Using Affinity-Guided, Multivalent Organocatalysts

inferredcites →https://doi.org/10.1021/ja205602jopenalex-snapshot

Enantioselective Acylation of Silyl Ketene Acetals through Fluoride Anion-Binding Catalysis

inferredcites →https://doi.org/10.1021/ja307425gopenalex-snapshot

Nonenzymatic Dynamic Kinetic Resolution of Secondary Alcohols via Enantioselective Acylation: Synthetic and Mechanistic Studies

inferredcites →https://doi.org/10.1021/ja805390kopenalex-snapshot

Enantioselective Organocatalytic Direct Michael Addition of Nitroalkanes to Nitroalkenes Promoted by a Unique Bifunctional DMAP-Thiourea

inferredcites →https://doi.org/10.1021/ja9079435openalex-snapshot

Merging Nucleophilic and Hydrogen Bonding Catalysis: An Anion Binding Approach to the Kinetic Resolution of Amines

inferredcites →https://doi.org/10.1021/ja953631fopenalex-snapshot

Kinetic Resolution of Secondary Alcohols. Enantioselective Acylation Mediated by a Chiral (Dimethylamino)pyridine Derivative

inferredcites →https://doi.org/10.1021/ja963275gopenalex-snapshot

Nonenzymatic Kinetic Resolution of Racemic Alcohols through an “Induced Fit” Process

inferredcites →https://doi.org/10.1021/ja963835bopenalex-snapshot

Effective Kinetic Resolution of Secondary Alcohols with a Planar−Chiral Analogue of 4-(Dimethylamino)pyridine. Use of the Fe(C5Ph5) Group in Asymmetric Catalysis

inferredcites →https://doi.org/10.1021/la962125gopenalex-snapshot

Effects of Surfactants on Solvolysis of p-Nitrophenyl Alkanoates Catalyzed by 4-(Dialkylamino)pyridine-Functionalized Polymer in Aqueous Methanol Solution

inferredcites →https://doi.org/10.1021/ma00010a006openalex-snapshot

Synthesis, characterization, and solubility behavior of polysiloxanes with 4-(dialkylamino)pyridine functions

inferredcites →https://doi.org/10.1021/ma00219a025openalex-snapshot

New transacylation catalysts: silanes and siloxanes functionalized with 4-(dialkylamino)pyridine moieties

inferredcites →https://doi.org/10.1021/ol053050nopenalex-snapshot

A Metallocene-Pyrrolidinopyridine Nucleophilic Catalyst for Asymmetric Synthesis

inferredcites →https://doi.org/10.1021/ol062712lopenalex-snapshot

Development of More Potent 4-Dimethylaminopyridine Analogues

inferredcites →https://doi.org/10.1021/ol1029589openalex-snapshot

Synthesis and Reactivity of Highly Nucleophilic Pyridines

inferredcites →https://doi.org/10.1021/ol2001705openalex-snapshot

Design, Synthesis, and Evaluation of a Helicenoidal DMAP Lewis Base Catalyst

inferredcites →https://doi.org/10.1039/b002041iopenalex-snapshot

The kinetic resolution of allylic alcohols by a non-enzymatic acylation catalyst; application to natural product synthesis

inferredcites →https://doi.org/10.1039/b307425kopenalex-snapshot

Dendronized cyclocopolymers with a radial gradient of polarity and their use to catalyze a difficult esterification

inferredcites →https://doi.org/10.1039/b309117aopenalex-snapshot

Heterogeneous Baylis–Hillman using a polystyrene-bound 4-(N-benzyl-N-methylamino)pyridine as reusable catalyst

inferredcites →https://doi.org/10.1039/c1cc11556aopenalex-snapshot

A salt made of 4-N,N-dimethylaminopyridine (DMAP) and saccharin as an efficient recyclable acylation catalyst: a new bridge between heterogeneous and homogeneous catalysis

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.4749827openalex-extracted

A One-Step Synthesis of Esters Via Modified Yamaguchi Esterification Mediated by Pivaloyl Anhydride

inferred← citeshttps://doi.org/10.1002/9780471264194.fos04311.pub6openalex-snapshot

4‐Dimethylaminopyridine ( DMAP )

inferred← citeshttps://doi.org/10.1002/adsc.201600997openalex-snapshot

Sulfination of Alcohols with p ‐Toluenesulfonylmethyl Isocyanide under Metal‐Free Conditions: A Mitsunobu Approach

inferred← citeshttps://doi.org/10.1002/ajoc.70414openalex-snapshot

A Sustainable Approach to Synthesize Tetra‐ and Penta‐Substituted Pyrroles Under Three‐Component One‐Pot Synthesis Using Novel Thiourea‐Derived Organocatalysts

inferred← citeshttps://doi.org/10.1002/ange.201608046openalex-snapshot

Exploiting the Imidazolium Effect in Base‐free Ammonium Enolate Generation: Synthetic and Mechanistic Studies

inferred← citeshttps://doi.org/10.1002/ange.202016220openalex-snapshot

Enantioselective Synthesis of α‐Aryl‐β2‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201608046openalex-snapshot

Exploiting the Imidazolium Effect in Base‐free Ammonium Enolate Generation: Synthetic and Mechanistic Studies

inferred← citeshttps://doi.org/10.1002/anie.202016220openalex-snapshot

Enantioselective Synthesis of α‐Aryl‐β2‐Amino‐Esters by Cooperative Isothiourea and Brønsted Acid Catalysis

inferred← citeshttps://doi.org/10.1002/aoc.4741openalex-snapshot

Oxime palladacycle in PEG as a highly efficient and recyclable catalytic system for phenoxycarbonylation of aryl iodides with phenols

inferred← citeshttps://doi.org/10.1002/aoc.6073openalex-snapshot

Copper‐mediated simple and direct aerobic oxidative esterification of arylacetonitriles with alcohols/phenols

inferred← citeshttps://doi.org/10.1002/chem.202401402openalex-snapshot

Effect of Brønsted Acids on the Activation of Mixed Anhydride/Mixed Carbonic Anhydride and C‐Terminal‐Free N‐Methylated Peptide Synthesis in a Micro‐Flow Reactor

inferred← citeshttps://doi.org/10.1002/chin.201423056openalex-snapshot

ChemInform Abstract: 4‐(N,N‐Dimethylamino)pyridine Hydrochloride as a Recyclable Catalyst for Acylation of Inert Alcohols: Substrate Scope and Reaction Mechanism.

inferred← citeshttps://doi.org/10.1002/cjoc.201500190openalex-snapshot

TBHP/TEMPO‐Mediated Oxidative Synthesis of Imides from Amides

inferred← citeshttps://doi.org/10.1002/cjoc.201600285openalex-snapshot

Synthesis of 3′,4′‐Diaryl‐4′H‐spiro[indoline‐3,5′‐[1′,2′,4′]oxadiazol]‐2‐ones via DMAP‐catalyzed Domino Reactions and Their Antibacterial Activity

inferred← citeshttps://doi.org/10.1002/cplu.202400741openalex-snapshot

Novel DMAP@Mesoporous Silica Hybrid Heterogeneous Catalysts for the Knoevenagel Condensation: Greener Synthesis through Eco‐friendly Solvents

inferred← citeshttps://doi.org/10.1002/cssc.202502649openalex-snapshot

A Three‐Step Route to Functionalized Pyrrole‐2,5‐Dicarboxylic Acids from Galactaric Acid

inferred← citeshttps://doi.org/10.1002/ejic.202500197openalex-snapshot

Bioinspired Cobalt Amino Acid Complexes for Synthesis of Polyester Polyols from Epoxide and Cyclic Anhydride

inferred← citeshttps://doi.org/10.1002/ejoc.201403624openalex-snapshot

Copper‐Catalyzed Synthesis of Imides from Aldehydes or Alcohols and Amine Hydrochloride Salts

inferred← citeshttps://doi.org/10.1002/ejoc.201600496openalex-snapshot

Efficient O‐Acylation of Alcohols and Phenol Using Cp2TiCl as a Reaction Promoter

inferred← citeshttps://doi.org/10.1002/pi.4959openalex-snapshot

Polymethacrylates containing a 4‐amino‐pyridyl derivative covalently attached as effective catalysts in acylation chemistry: self‐activation by neighboring group effects

inferred← citeshttps://doi.org/10.1002/pi.5058openalex-snapshot

Catalytic performance of methacrylate‐based poly‐4‐(dialkylamino)‐pyridines: activity prediction via NMR shifts

inferred← citeshttps://doi.org/10.1002/slct.201600824openalex-snapshot

Synthesis of a Novel Magnetic Reusable Organocatalyst Based on 4‐Dialkylaminopyridines for Acyl Transformations

inferred← citeshttps://doi.org/10.1007/978-1-4939-7366-8_12openalex-snapshot

High-Throughput Screening Assays for Lipolytic Enzymes

inferred← citeshttps://doi.org/10.1007/s00706-016-1897-1openalex-snapshot

Reusable and efficient polyvinylpolypyrrolidone-supported triflic acid catalyst for acylation of alcohols, phenols, amines, and thiols under solvent-free conditions

inferred← citeshttps://doi.org/10.1007/s10098-016-1316-7openalex-snapshot

Novel alkali-promoted hydrotalcite for selective synthesis of 2-methoxy phenyl benzoate from guaiacol and benzoic anhydride

inferred← citeshttps://doi.org/10.1007/s10562-022-03933-4openalex-snapshot

A Novel Nanoencapsulated Zirconium(IV) Chloride Using Non-cross-linked Polystyrene as a Recyclable Lewis Acid Catalyst: Synthesis, Characterization, and Performance Towards Acylation of Alcohols and Phenols

inferred← citeshttps://doi.org/10.1007/s12039-018-1461-0openalex-snapshot

A potential greener protocol for peptide coupling reactions using recyclable/reusable ionic liquid [ $$\hbox {C}_{4}\hbox {-DABCO}][\hbox {N(CN)}_{2}$$ C 4 -DABCO ] [ N(CN) 2 ]

inferred← citeshttps://doi.org/10.1007/s13738-014-0542-3openalex-snapshot

One-pot synthesis of 1,2,4-oxadiazoles from carboxylic acids using 4-(dimethylamino)pyridinium acetate as efficient, regenerable, and green catalyst with ionic liquid character

inferred← citeshttps://doi.org/10.1007/s13738-015-0711-zopenalex-snapshot

Highly efficient and recyclable acetylation of phenols and alcohols by nickel zirconium phosphate under solvent-free conditions

inferred← citeshttps://doi.org/10.1016/j.arabjc.2015.06.012openalex-snapshot

Recent advances in 4-hydroxycoumarin chemistry. Part 1: Synthesis and reactions

inferred← citeshttps://doi.org/10.1016/j.clay.2022.106695openalex-snapshot

Solvent free selective acylation of phenol by HF–modified saponite catalysts

inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2017.03.027openalex-snapshot

Fluorinated bis-GMA as potential monomers for dental restorative composite materials

inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2020.109570openalex-snapshot

Biocompatible and low-cost pyridinium halides catalysts promoted ring-opening polymerizations of cyclic esters in bulk

inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e31798openalex-snapshot

Highly efficient CdS/CeO2/Ag3PO4 nanocomposite as novel heterogenous catalyst for Knoevenagel condensation and acetylation reactions

inferred← citeshttps://doi.org/10.1016/j.jcat.2023.03.023openalex-snapshot

Cobalt-catalyzed carbonylative acetylation of phenols

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122264openalex-snapshot

Noncross-linked polystyrene nanoencapsulation of ferric chloride: A novel and reusable heterogeneous macromolecular Lewis acid catalyst toward selective acetylation of alcohols, phenols, amines, and thiols

inferred← citeshttps://doi.org/10.1016/j.mcat.2019.110672openalex-snapshot

Supramolecular Pd(II) complex of DPPF and dithiolate: An efficient catalyst for amino and phenoxycarbonylation using Co2(CO)8 as sustainable C1 source

inferred← citeshttps://doi.org/10.1016/j.molcata.2015.04.002openalex-snapshot

Magnetically separable γ-Fe2O3 nanoparticles: An efficient catalyst for acylation of alcohols, phenols, and amines using sonication energy under solvent free condition

inferred← citeshttps://doi.org/10.1016/j.molliq.2025.128378openalex-snapshot

Exploring the physicochemical and quantum chemical investigation on N,N-dimethyl-4-aminopyridinium-2,4-dihydroxybenzoate monohydrate: An organic salt crystal for biological applications

inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.02.002openalex-snapshot

Synthesis and studies on structural, optical and nonlinear optical properties of novel organic inter-molecular compounds: 4-chloro-3-nitroaniline−3-hydroxy benzaldehyde and urea−4-dimethylaminopyridine

inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2016.04.015openalex-snapshot

DMAP-based flexible polymer networks formed via Heck coupling as efficient heterogeneous organocatalysts

inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.001openalex-snapshot

Intramolecular functionalization of C(sp 3 ) H bonds adjacent to an amide nitrogen atom: Metal-free synthesis of 2-hydroxy-benzoxazinone derivatives

inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.12.106openalex-snapshot

4-(N,N-Dimethylamino)pyridinium acetate as a recyclable catalyst for the synthesis of 5-substituted-1H-tetrazoles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.11.038openalex-snapshot

A convenient one-pot synthesis of ketone cyanohydrin esters in aqueous media

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152197openalex-snapshot

An alternative route for boron phenoxide preparation from arylboronic acid and its application for C O bond formation

inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155797openalex-snapshot

Synthesis of phenyl carboxylates via molybdenum carbonyl-mediated carbonylation of phenols and iodides under mild conditions

inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60185-6openalex-snapshot

Acetylation of alcohols and phenols under solvent-free conditions using copper zirconium phosphate

inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60280-1openalex-snapshot

Acetylation of alcohols and phenols under solvent-free conditions using iron zirconium phosphate

inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00674openalex-snapshot

Preparation and Reactivity of Organometallic Reagents Leading to Functionalized N -Heteroaromatics

inferred← citeshttps://doi.org/10.1021/acs.iecr.5c00796openalex-snapshot

A New Approach to Thickening Polymers through the Esterification Reaction of Poly(styrene-alt-maleic anhydride) and Sugar (Alcohol)

inferred← citeshttps://doi.org/10.1021/acs.joc.0c02473openalex-snapshot

Influence of Anion-Binding Schreiner’s Thiourea on DMAP Salts: Synergistic Catalysis toward the Stereoselective Dehydrative Glycosylation from 2-Deoxyhemiacetals

inferred← citeshttps://doi.org/10.1021/acs.joc.0c02848openalex-snapshot

Size-Driven Inversion of Selectivity in Esterification Reactions: Secondary Beat Primary Alcohols

inferred← citeshttps://doi.org/10.1021/acs.joc.3c01052openalex-snapshot

Recyclable Polymer Supported DMAP Catalyzed Cascade Synthesis of α-Pyrones

inferred← citeshttps://doi.org/10.1021/acs.joc.4c02662openalex-snapshot

Visible-Light-Induced Synthesis of Esters via a Self-Propagating Radical Reaction

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02799openalex-snapshot

Photoredox/Copper Dual-Catalyzed Remote C(sp 3 )-H Acyloxylation of N -Fluorocarboxamides

inferred← citeshttps://doi.org/10.1021/acs.joc.6b00408openalex-snapshot

Synthesis of Esters by in Situ Formation and Trapping of Diazoalkanes

inferred← citeshttps://doi.org/10.1021/acs.joc.6c00105openalex-snapshot

Breaking the Aromaticity Trap: N -Silylation-Induced Formation of Stable 2,3-Dihydro-4-dialkylaminopyridin-1-iums

inferred← citeshttps://doi.org/10.1021/acs.joc.8b02567openalex-snapshot

Base-Promoted Amidation and Esterification of Imidazolium Salts via Acyl C–C bond Cleavage: Access to Aromatic Amides and Esters

inferred← citeshttps://doi.org/10.1021/acs.macromol.5c03257openalex-snapshot

Degradable Telechelic Polythioesters from Activated Diesters and Their Site-Selective End-Group Functionalization

inferred← citeshttps://doi.org/10.1021/acs.oprd.3c00081openalex-snapshot

Coaxial Dielectric Spectroscopy as an In-Line Process Analytical Technique for Reaction Monitoring

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01383openalex-snapshot

Sulfanylmethyldimethylaminopyridine as a Useful Thiol Additive for Ligation Chemistry in Peptide/Protein Synthesis

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03528openalex-snapshot

An Approach to the Synthesis of Electron-Rich and Hindered Esters and Its Application to the Synthesis of Acteoside

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00763openalex-snapshot

Photoredox/Copper Dual-Catalyzed Benzylic C–H Esterification via Radical-Polar Crossover

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02851openalex-snapshot

Copper-Catalyzed Selective C(sp3)–H Esterification Using Azidobenziodoxole Derivatives as the Mediator

inferred← citeshttps://doi.org/10.1021/acscatal.0c03702openalex-snapshot

Tropolonate Salts as Acyl-Transfer Catalysts under Thermal and Photochemical Conditions: Reaction Scope and Mechanistic Insights

inferred← citeshttps://doi.org/10.1021/acssuschemeng.6c03025openalex-snapshot

Integrating Life Cycle Assessment with Scale-Up Modeling and Machine Learning for Greener Pharmaceutics: The Case of (−)-Chloramphenicol

inferred← citeshttps://doi.org/10.1021/op500394fopenalex-snapshot

A DMAP-Catalyzed Approach to the Industrial-Scale Preparation of N -6-Demethylated 9,10-Dihydrolysergic Acid Methyl Ester: A Key Cabergoline and Pergolide Precursor

inferred← citeshttps://doi.org/10.1038/s41557-023-01315-wopenalex-snapshot

Aromatic pentaamide macrocycles bind anions with high affinity for transport across biomembranes

inferred← citeshttps://doi.org/10.1038/s41598-021-86475-wopenalex-snapshot

Synthesis process optimization and field trials of insecticide candidate NKY-312

inferred← citeshttps://doi.org/10.1038/s41598-025-01567-1openalex-snapshot

CdS/CeO2/Ag2CO3 nanocomposite as an efficient heterogeneous catalyst for Knoevenagel condensation and acetylation reactions

inferred← citeshttps://doi.org/10.1039/c5nj00655dopenalex-snapshot

A novel nickel-catalyzed synthesis of thioesters, esters and amides from aryl iodides in the presence of chromium hexacarbonyl

inferred← citeshttps://doi.org/10.1039/c5ob00806aopenalex-snapshot

4-(Dimethylamino)pyridine-catalysed iodolactonisation of γ,δ-unsaturated carboxylic acids

inferred← citeshttps://doi.org/10.1039/c6ra22757kopenalex-snapshot

An extremely efficient and green method for the acylation of secondary alcohols, phenols and naphthols with a deep eutectic solvent as the catalyst

inferred← citeshttps://doi.org/10.1039/c6ra23696kopenalex-snapshot

Polymer supported DMAP: an easily recyclable organocatalyst for highly atom-economical Henry reaction under solvent-free conditions

inferred← citeshttps://doi.org/10.1039/c7cc02828hopenalex-snapshot

Practical in situ-generation of phosphinite ligands for palladium-catalyzed carbonylation of (hetero)aryl bromides forming esters

inferred← citeshttps://doi.org/10.1039/c7ra00196gopenalex-snapshot

Zinc porphyrin/fullerene/block copolymer micelle for enhanced electron transfer ability and stability

inferred← citeshttps://doi.org/10.1039/d0gc03731aopenalex-snapshot

Environmentally benign decarboxylative N -, O -, and S -acetylations and acylations

inferred← citeshttps://doi.org/10.1039/d0nj05050dopenalex-snapshot

An efficient method to prepare aryl acetates by the carbonylation of aryl methyl ethers or phenols

inferred← citeshttps://doi.org/10.1039/d2nj04326bopenalex-snapshot

Ligand-free access to benzisothiazolones and benzisoselenazolones through NiFe 2 O 4 catalyzed concomitant annulation of 2-halobenzanilides with chalcogens and their late-stage transformations

inferred← citeshttps://doi.org/10.1039/d3gc03074aopenalex-snapshot

Soybean oil derived-process oil prepared via recyclable organocatalysis for eco-friendly styrene–butadiene rubber composites

inferred← citeshttps://doi.org/10.1039/d4cc03521fopenalex-snapshot

One-pot synthesis of functionalized dihydropyridin-2-ones via carbene-catalyzed base-controlled [3+3] annulation reaction

inferred← citeshttps://doi.org/10.1080/10406638.2022.2061533openalex-snapshot

Steglich’s Base Catalyzed Three-Component Synthesis of Isoxazol-5-Ones

inferred← citeshttps://doi.org/10.1080/17518253.2026.2697575openalex-snapshot

A green facile approach for the synthesis of benzoxazoles and benzimidazoles by reductive cyclization by hydrosilane under air conditions

inferred← citeshttps://doi.org/10.1093/mtomcs/mfad023openalex-snapshot

Ferrocenoyl-substituted quinolinone and coumarin as organometallic inhibitors of SARS-CoV-2 3CLpro main protease

inferred← citeshttps://doi.org/10.1126/science.abj0999openalex-snapshot

Accelerated dinuclear palladium catalyst identification through unsupervised machine learning

inferred← citeshttps://doi.org/10.1134/s1070428025603504openalex-snapshot

Pyrazine-Linked 1,2,3-Triazole Derivatives: Synthesis, Characterization, In Vitro Antimicrobial Evaluation, and Docking Study

inferred← citeshttps://doi.org/10.1515/gps-2019-0003openalex-snapshot

Use of deep eutectic solvents as catalyst: A mini-review

inferred← citeshttps://doi.org/10.2139/ssrn.7244084openalex-snapshot

DMAP.saccharin as a Recyclable Organocatalyst for the Acylation of Carbohydrates Under Solvent-Free Conditions

inferred← citeshttps://doi.org/10.2174/2213337207999200731184638openalex-snapshot

Iron (III) Chloride Hexahydrate as a Highly Efficient Catalyst for Acetylation of Protic Nucleophiles with Acetic Anhydride under Solvent-free Conditions

inferred← citeshttps://doi.org/10.3390/chemistry1010006openalex-snapshot

Acetylation of Alcohols, Amines, Phenols, Thiols under Catalyst and Solvent-Free Conditions

inferred← citeshttps://doi.org/10.3390/chemistry7040131openalex-snapshot

Desulfurative Acetoxylation of Alkyl Benzyl Phenyl Sulfides

inferred← citeshttps://doi.org/10.3390/molecules29184418openalex-snapshot

2-Bromopyridines as Versatile Synthons for Heteroarylated 2-Pyridones via Ru(II)-Mediated Domino C–O/C–N/C–C Bond Formation Reactions

inferred← citeshttps://doi.org/10.3390/molecules30132787openalex-snapshot

Solid-Phase Oligosaccharide Synthesis with Highly Complexed Peptidoglycan Fragments

inferred← citeshttps://doi.org/10.4236/ojmc.2015.52003openalex-snapshot

Synthesis and Bioactivity of Natural Occurring Petasin-Like Derivatives as Antitumor Agents

inferred← citeshttps://doi.org/10.6023/cjoc202406015openalex-snapshot

Metal-Free, Photo-Catalyzed Oxidation of Benzylic C—H Bonds to Access Carbonyl Functionality

inferred← citeshttps://doi.org/10.70675/0d6d95aczd210z43a2zb94dz18e5bc39d3daopenalex-snapshot

Dédoublement cinétique d'amines par transfert d'acyle et approche synthétique du lyngbouilloside

inferred← citeshttps://doi.org/10.70675/0e544a84zde16z400ez8888zcee6e1e71defopenalex-snapshot

Etude du système Myrosinase-Glucosinolate comme outil de bioconjugaison

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.