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Organic Synthesis “On Water”
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471221902openalex-snapshot
Synthetic Applications of 1,3‐Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
inferredcites →https://doi.org/10.1002/1521-3773(20010601)40:11<2004::aid-anie2004>3.0.co;2-5openalex-snapshot
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4openalex-snapshot
A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
inferredcites →https://doi.org/10.1002/1522-2675(20000809)83:8<1734::aid-hlca1734>3.0.co;2-eopenalex-snapshot
Applications of Aziridinium Ions: Selective Syntheses of Pyrazolidin-3-ones and Pyrazolo[1,2-a]pyrazoles
inferredcites →https://doi.org/10.1002/1522-2675(20010228)84:2<513::aid-hlca513>3.0.co;2-sopenalex-snapshot
`Inverse-Electron-Demand'Diels-Alder Reactions of (E)-3-Diazenylbut-2-enes in Water
inferredcites →https://doi.org/10.1002/3527605118.ch11openalex-snapshot
Applications of Multicomponent Reactions in Drug Discovery – Lead Generation to Process Development
inferredcites →https://doi.org/10.1002/3527607862.ch12openalex-snapshot
Epoxides and Aziridines in Click Chemistry
inferredcites →https://doi.org/10.1002/adsc.200390052openalex-snapshot
AgOTf‐Catalyzed Aza‐Diels–Alder Reactions of Danishefsky's Diene with Imines in Water
inferredcites →https://doi.org/10.1002/adsc.200606090openalex-snapshot
Catalyzed Reactions of Alkynes in Water
inferredcites →https://doi.org/10.1002/adsc.200606118openalex-snapshot
Diastereoselective Synthesis of α‐Oxyamines via Gold‐, Silver‐ and Copper‐Catalyzed, Three‐Component Couplings of α‐Oxyaldehydes, Alkynes, and Amines in Water
inferredcites →https://doi.org/10.1002/adsc.200606136openalex-snapshot
Alkylation of Aldehydes with Trialkylboranes in Water
inferredcites →https://doi.org/10.1002/adsc.200800114openalex-snapshot
Ring‐Closing Metathesis at Room Temperature within Nanometer Micelles using Water as the Only Solvent
inferredcites →https://doi.org/10.1002/ange.200602122openalex-snapshot
On Water and in Air: Fast and Highly Chemoselective Transfer Hydrogenation of Aldehydes with Iridium Catalysts
inferredcites →https://doi.org/10.1002/ange.200705347openalex-snapshot
Highly Efficient Organic Reactions “on Water”, “in Water”, and Both
inferredcites →https://doi.org/10.1002/anie.196305651openalex-snapshot
1,3‐Dipolar Cycloadditions. Past and Future
inferredcites →https://doi.org/10.1002/anie.199315451openalex-snapshot
Hydrophobic Effects. Opinions and Facts
inferredcites →https://doi.org/10.1002/anie.199502591openalex-snapshot
Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
inferredcites →https://doi.org/10.1002/anie.200461496openalex-snapshot
Mechanism of the Ligand‐Free Cu I ‐Catalyzed Azide–Alkyne Cycloaddition Reaction
inferredcites →https://doi.org/10.1002/anie.200462211openalex-snapshot
Biomimetic Total Synthesis of Gambogin and Rate Acceleration of Pericyclic Reactions in Aqueous Media
inferredcites →https://doi.org/10.1002/anie.200462883openalex-snapshot
“On Water”: Unique Reactivity of Organic Compounds in Aqueous Suspension
inferredcites →https://doi.org/10.1002/anie.200502017openalex-snapshot
General Catalysts for the Suzuki–Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water
inferredcites →https://doi.org/10.1002/anie.200601392openalex-snapshot
Enamine‐Based Aldol Organocatalysis in Water: Are They Really “All Wet”?
inferredcites →https://doi.org/10.1002/anie.200602122openalex-snapshot
On Water and in Air: Fast and Highly Chemoselective Transfer Hydrogenation of Aldehydes with Iridium Catalysts
inferredcites →https://doi.org/10.1002/anie.200602585openalex-snapshot
Intermolecular Rhodium‐Catalyzed Carbometalation/Heck‐Type Reaction in Water
inferredcites →https://doi.org/10.1002/anie.200603378openalex-snapshot
In Water or in the Presence of Water?
inferredcites →https://doi.org/10.1002/anie.200604952openalex-snapshot
Water in Organocatalytic Processes: Debunking the Myths
inferredcites →https://doi.org/10.1002/anie.200702141openalex-snapshot
Direct Arylation of Thiazoles on Water
inferredcites →https://doi.org/10.1002/anie.200705347openalex-snapshot
Highly Efficient Organic Reactions “on Water”, “in Water”, and Both
inferredcites →https://doi.org/10.1002/anie.200800160openalex-snapshot
A Highly Efficient and Selective Au I ‐Catalyzed Tandem Synthesis of Diversely Substituted Pyrrolo[1,2‐ a ]quinolines in Aqueous Media
inferredcites →https://doi.org/10.1002/anie.200800622openalex-snapshot
A Rational Approach towards the Nucleophilic Substitutions of Alcohols “on Water”
inferredcites →https://doi.org/10.1002/cber.186900201183openalex-snapshot
Beiträge zur Kenntniss des Acetenylbenzols
inferredcites →https://doi.org/10.1002/cber.188201502274openalex-snapshot
Darstellung von Indigblau aus Orthonitrobenzaldehyd
inferredcites →https://doi.org/10.1002/cber.188501801145openalex-snapshot
Ueber Polyacetylenverbindungen
inferredcites →https://doi.org/10.1002/chem.200601737openalex-snapshot
Simple and Efficient Recyclable Catalytic System for Performing Copper‐Catalysed S‐Arylation Reactions in the Presence of Water
inferredcites →https://doi.org/10.1002/chem.200700227openalex-snapshot
Dual Reactivity Pattern of Allenolates “On Water”: The Chemical Basis for Efficient Allenolate‐Driven Organocatalytic Systems
inferredcites →https://doi.org/10.1002/ejoc.200500483openalex-snapshot
CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
inferredcites →https://doi.org/10.1002/ejoc.200500863openalex-snapshot
“On Water”‐Promoted Direct Coupling of Indoles with 1,4‐Benzoquinones without Catalyst
inferredcites →https://doi.org/10.1002/ejoc.200800092openalex-snapshot
Nucleophilic Reactivities of Pyrroles
inferredcites →https://doi.org/10.1002/hlca.200590128openalex-snapshot
Water and the Huisgen Cycloaddition Reaction: A Focus on Polar Contributions to the Transition State in the Reactions of Dicyano(phthalazinium)methanide with Substituted Styrenes and Benzylidene Acetones
inferredcites →https://doi.org/10.1002/jlac.18701540202openalex-snapshot
Untersuchungen über einige Derivate der Zimmtsäure
inferredcites →https://doi.org/10.1002/jlac.19053420204openalex-snapshot
Zur Kenntniss der Acetylenbindung
inferredcites →https://doi.org/10.1002/poc.1325openalex-snapshot
Do general nucleophilicity scales exist?
inferredcites →https://doi.org/10.1002/tcr.10021openalex-snapshot
The Use of Hydrophilic Groups in Aqueous Organic Reactions
inferredcites →https://doi.org/10.1007/s10098-003-0242-7openalex-snapshot
Water as a reaction medium for clean chemical processes
inferredcites →https://doi.org/10.1007/s10098-004-0262-yopenalex-snapshot
Water as a reaction medium for clean chemical processes
inferredcites →https://doi.org/10.1016/0040-4039(95)00987-nopenalex-snapshot
1,3-Dipolar Cycloaddition of Phenyl Azide to Norbornene in Aqueous Solutions
inferredcites →https://doi.org/10.1016/0040-4039(95)02255-4openalex-snapshot
Catalytic coupling of terminal acetylenes with iodoarenes and diaryliodonium salts in water
inferredcites →https://doi.org/10.1016/j.jfluchem.2007.06.010openalex-snapshot
A novel synthesis of 5-perfluorophenyl 4,5-dihydro-1H-pyrazoles in THF or water
inferredcites →https://doi.org/10.1016/j.tet.2005.08.068openalex-snapshot
Aqueous medium effects on multi-component reactions
inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.038openalex-snapshot
Facile and selective copper–palladium catalyzed addition of terminal alkynes to activated alkynes in water
inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.089openalex-snapshot
1,3-Dipolar cycloaddition of azides with electron-deficient alkynes under mild condition in water
inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.131openalex-snapshot
Palladium catalyzed alkynylation of aryl halides (Sonogashira reaction) in water
inferredcites →https://doi.org/10.1016/j.tetlet.2005.12.040openalex-snapshot
Visible light induced ‘on water’ benzylic bromination with N-bromosuccinimide
inferredcites →https://doi.org/10.1016/j.tetlet.2006.04.119openalex-snapshot
Directed regioselectivity of bromination of ketones with NBS: solvent-free conditions versus water
inferredcites →https://doi.org/10.1016/j.tetlet.2007.03.119openalex-snapshot
Organic synthesis in water: 1,3-dipolar cycloaddition reactions at ambient temperature with aqueous suspensions of solid reactants
inferredcites →https://doi.org/10.1016/s0040-4020(01)89795-7openalex-snapshot
Water-promoted organic reactions. aldol reaction of silyl enol ethers with carbonyl compounds under atmospheric pressure and neutral conditions.
inferredcites →https://doi.org/10.1016/s0040-4020(01)90093-6openalex-snapshot
Solvent effect as the result of frontier molecular orbital interaction. V. Diels-Alder with heterodienophiles: a unified approach to the solvent effect of the Diels-Alder reactions
inferredcites →https://doi.org/10.1016/s0040-4039(00)61625-8openalex-snapshot
The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines
inferredcites →https://doi.org/10.1016/s0040-4039(00)81800-6openalex-snapshot
“Micellar” catalysis in the aqueous intermolecular diels-alder reaction: rate acceleration and enhanced selectivity
inferredcites →https://doi.org/10.1016/s0040-4039(00)81801-8openalex-snapshot
Selective diels-alder reactions in aqueous solutions and suspensions
inferredcites →https://doi.org/10.1016/s1367-5931(02)00328-9openalex-snapshot
Recent advances in isocyanide-based multicomponent chemistry
inferredcites →https://doi.org/10.1021/ar00006a001openalex-snapshot
Hydrophobic effects on simple organic reactions in water
inferredcites →https://doi.org/10.1021/ar000145aopenalex-snapshot
Development of Novel Lewis Acid Catalysts for Selective Organic Reactions in Aqueous Media
inferredcites →https://doi.org/10.1021/ar7002732openalex-snapshot
Integration or Segregation: How Do Molecules Behave at Oil/Water Interfaces?
inferredcites →https://doi.org/10.1021/cr00022a004openalex-snapshot
Organic reactions in aqueous media - with a focus on carbon-carbon bond formation
inferredcites →https://doi.org/10.1021/cr00039a007openalex-snapshot
Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
inferredcites →https://doi.org/10.1021/cr0006831openalex-snapshot
Water Structure from Scattering Experiments and Simulation
inferredcites →https://doi.org/10.1021/cr010122popenalex-snapshot
Stereoselective Organic Reactions in Water
inferredcites →https://doi.org/10.1021/cr030009uopenalex-snapshot
Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update
inferredcites →https://doi.org/10.1021/cr040377dopenalex-snapshot
Sum-Frequency Vibrational Spectroscopy on Water Interfaces: Polar Orientation of Water Molecules at Interfaces
inferredcites →https://doi.org/10.1021/cr0509410openalex-snapshot
Microwave-Assisted Synthesis in Water as Solvent
inferredcites →https://doi.org/10.1021/cr60135a004openalex-snapshot
Brominations with N-Bromosuccinimide and Related Compounds. The Wohl-Ziegler Reaction.
inferredcites →https://doi.org/10.1021/ja00039a074openalex-snapshot
Initial-state and transition-state effects on Diels-Alder reactions in water and mixed aqueous solvents
inferredcites →https://doi.org/10.1021/ja00238a029openalex-snapshot
The mechanism of rearrangement of chorismic acid and related compounds
inferredcites →https://doi.org/10.1021/ja00546a048openalex-snapshot
Hydrophobic acceleration of Diels-Alder reactions
inferredcites →https://doi.org/10.1021/ja010600dopenalex-snapshot
Is the tert-Butyl Chloride Solvolysis the Most Misunderstood Reaction in Organic Chemistry? Evidence Against Nucleophilic Solvent Participation in the tert-Butyl Chloride Transition State and for Increased Hydrogen Bond Donation to the 1-Adamantyl Chloride Solvolysis Transition State
inferredcites →https://doi.org/10.1021/ja01614a056openalex-snapshot
Bromohydrins from Olefins and N-Bromosuccinimide in Water
inferredcites →https://doi.org/10.1021/ja0206644openalex-snapshot
Mechanisms of Tetrazole Formation by Addition of Azide to Nitriles
inferredcites →https://doi.org/10.1021/ja026007topenalex-snapshot
Enantioselective Direct-Addition of Terminal Alkynes to Imines Catalyzed by Copper(I)pybox Complex in Water and in Toluene
inferredcites →https://doi.org/10.1021/ja030204qopenalex-snapshot
Why Is Tetrazole Formation by Addition of Azide to Organic Nitriles Catalyzed by Zinc(II) Salts?
inferredcites →https://doi.org/10.1021/ja0359299openalex-snapshot
A Highly Efficient Three-Component Coupling of Aldehyde, Alkyne, and Amines via C−H Activation Catalyzed by Gold in Water
inferredcites →https://doi.org/10.1021/ja038583aopenalex-snapshot
Multicomponent Reactions Are Accelerated in Water
inferredcites →https://doi.org/10.1021/ja0471525openalex-snapshot
Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and Intermediates
inferredcites →https://doi.org/10.1021/ja063609uopenalex-snapshot
Functionalization of Single-Walled Carbon Nanotubes “On Water”
inferredcites →https://doi.org/10.1021/ja068120fopenalex-snapshot
On the Theory of Organic Catalysis “on Water”
inferredcites →https://doi.org/10.1021/ja072679dopenalex-snapshot
Ligand-Accelerated Cu-Catalyzed Azide−Alkyne Cycloaddition: A Mechanistic Report
inferredcites →https://doi.org/10.1021/ja963178nopenalex-snapshot
A New and Practical Synthesis of α-Amino Acids from Alkenyl Boronic Acids
inferredcites →https://doi.org/10.1021/jo00005a063openalex-snapshot
Amination of olefinic compounds with bis(2,2,2-trichloroethyl) azodicarboxylate
inferredcites →https://doi.org/10.1021/jo00046a036openalex-snapshot
A semitheoretical multiparameter approach to correlate solvent effects on reactions and equilibria
inferredcites →https://doi.org/10.1021/jo00071a042openalex-snapshot
Allylic amination by the Lewis acid-mediated ene reactions of diethyl azodicarboxylate with alkenes
inferredcites →https://doi.org/10.1021/jo00097a045openalex-snapshot
Diels-Alder Reactions in Water. Effects of Hydrophobicity and Hydrogen Bonding
inferredcites →https://doi.org/10.1021/jo00166a051openalex-snapshot
Aqueous intermolecular Diels-Alder chemistry: reactions of diene carboxylates with dienophiles in water at ambient temperature
inferredcites →https://doi.org/10.1021/jo00264a002openalex-snapshot
Effect of polar solvents on the rates of Claisen rearrangements: assessment of ionic character
inferredcites →https://doi.org/10.1021/jo00361a045openalex-snapshot
Water-promoted organic reactions: aldol reaction under neutral conditions
inferredcites →https://doi.org/10.1021/jo01047a008openalex-snapshot
The Substitution of Aryl Iodides with Cuprous Acetylides. A Synthesis of Tolanes and Heterocyclics 1
inferredcites →https://doi.org/10.1021/jo010635wopenalex-snapshot
Preparation of 5-Substituted 1 H -Tetrazoles from Nitriles in Water
inferredcites →https://doi.org/10.1021/jo011148jopenalex-snapshot
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
inferredcites →https://doi.org/10.1021/jo015632yopenalex-snapshot
2,6-Dichloro-9-thiabicyclo[3.3.1]nonane: A Privileged, Bivalent Scaffold for the Display of Nucleophilic Components
inferredcites →https://doi.org/10.1021/jo0349330openalex-snapshot
A Kinetic Study of 1,3-Dipolar Cycloadditions in Micellar Media
inferredcites →https://doi.org/10.1021/jo0489869openalex-snapshot
Nucleophilic Substitution by Grignard Reagents on Sulfur Mustards
inferredcites →https://doi.org/10.1021/jo060397aopenalex-snapshot
Rh(II)-Catalyzed Intramolecular C−H Insertion of Diazo Substrates in Water: Scope and Limitations
inferredcites →https://doi.org/10.1021/jo070665kopenalex-snapshot
Wittig Reactions in Water Media Employing Stabilized Ylides with Aldehydes. Synthesis of α,β-Unsaturated Esters from Mixing Aldehydes, α-Bromoesters, and Ph3P in Aqueous NaHCO3
inferredcites →https://doi.org/10.1021/jo8016633openalex-snapshot
A Nonsymmetric Pincer-Catalyzed Suzuki−Miyaura Arylation of Benzyl Halides and Other Nonactivated Unusual Coupling Partners
inferredcites →https://doi.org/10.1021/jo9614248openalex-snapshot
Solvent Effects on a Diels−Alder Reaction Involving a Cationic Diene: Consequences of the Absence of Hydrogen-Bond Interactions for Accelerations in Aqueous Media
inferredcites →https://doi.org/10.1021/jo980900mopenalex-snapshot
1,3-Dipolar Cycloadditions of Benzonitrile Oxide with Various Dipolarophiles in Aqueous Solutions. A Kinetic Study
inferredcites →https://doi.org/10.1021/jo981359xopenalex-snapshot
Effects of the Hydrophobicity of the Reactants on Diels−Alder Reactions in Water
inferredcites →https://doi.org/10.1021/jp020326popenalex-snapshot
QM/MM Simulations for Diels−Alder Reactions in Water: Contribution of Enhanced Hydrogen Bonding at the Transition State to the Solvent Effect
inferredcites →https://doi.org/10.1021/ol000221+openalex-snapshot
Applications of Aziridinium Ions. Selective Syntheses of α,β-Diamino Esters, α-Sulfanyl-β-amino Esters, β-Lactams, and 1,5-Benzodiazepin-2-one
inferredcites →https://doi.org/10.1021/ol051220qopenalex-snapshot
Highly Chemoselective Addition of Amines to Epoxides in Water
inferredcites →https://doi.org/10.1021/ol051546zopenalex-snapshot
Catalytic Asymmetric Ring Opening of meso-Epoxides with Aromatic Amines in Water
inferredcites →https://doi.org/10.1021/ol051684oopenalex-snapshot
Small Molecule Macroarray Construction via Ugi Four-Component Reactions
inferredcites →https://doi.org/10.1021/ol701886eopenalex-snapshot
Gold-Catalyzed Multicomponent Synthesis of Aminoindolizines from Aldehydes, Amines, and Alkynes under Solvent-Free Conditions or in Water
inferredcites →https://doi.org/10.1021/ol7020803openalex-snapshot
Radical Reactions in Aqueous Medium Using (Me3Si)3SiH
inferredcites →https://doi.org/10.1021/ol702755gopenalex-snapshot
Heck Couplings at Room Temperature in Nanometer Aqueous Micelles
inferredcites →https://doi.org/10.1021/ol800028xopenalex-snapshot
Olefin Cross-Metathesis Reactions at Room Temperature Using the Nonionic Amphiphile “PTS”: Just Add Water
inferredcites →https://doi.org/10.1021/ol801471fopenalex-snapshot
Sonogashira Couplings of Aryl Bromides: Room Temperature, Water Only, No Copper
inferredcites →https://doi.org/10.1021/ol801712eopenalex-snapshot
Micellar Catalysis of Suzuki−Miyaura Cross-Couplings with Heteroaromatics in Water
inferredcites →https://doi.org/10.1021/ol990256dopenalex-snapshot
Applications of Aziridinium Ions. Selective Syntheses of β-Aryl-α,β-diamino Esters
inferredcites →https://doi.org/10.1021/om700669vopenalex-snapshot
Enhanced Reactivity of Dinuclear Copper(I) Acetylides in Dipolar Cycloadditions
inferredcites →https://doi.org/10.1021/om800175aopenalex-snapshot
A Nonsymmetric Pincer-Type Palladium Catalyst In Suzuki, Sonogashira, and Hiyama Couplings in Neat Water
inferredcites →https://doi.org/10.1039/b302259eopenalex-snapshot
A highly regio- and stereoselective transition metal-catalyzed hydrosilylation of terminal alkynes under ambient conditions of air, water, and room temperature
inferredcites →https://doi.org/10.1039/b407936aopenalex-snapshot
The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones
inferredcites →https://doi.org/10.1039/b417089jopenalex-snapshot
Water-promoted direct aerobic oxidation of enol silyl ether to α-hydroxyl ketones without catalyst
inferredcites →https://doi.org/10.1039/b509436dopenalex-snapshot
Ligand-accelerated vanadium-catalysed epoxidation in water
inferredcites →https://doi.org/10.1039/b605850gopenalex-snapshot
Hydrophobic amplification of noncovalent organocatalysis
inferredcites →https://doi.org/10.1039/b606096jopenalex-snapshot
Organocatalysis “on water”. Regioselective [3 + 2]-cycloaddition of nitrones and allenolates
inferredcites →https://doi.org/10.1039/b612743fopenalex-snapshot
Highly efficient [2,3]-sigmatropic rearrangement of sulfur ylide derived from Rh( ii ) carbene and sulfides in water
inferredcites →https://doi.org/10.1039/b613014nopenalex-snapshot
The growing applications of click chemistry
inferredcites →https://doi.org/10.1039/b618340aopenalex-snapshot
Aqueous-phase asymmetric transfer hydrogenation of ketones ? a greener approach to chiral alcohols
inferredcites →https://doi.org/10.1039/b706926jopenalex-snapshot
µ-Acetylide and µ-alkenylidene ligands in “click” triazole syntheses
inferredcites →https://doi.org/10.1039/b707065aopenalex-snapshot
Bromination of ketones with H2O2–HBr “on water”
inferredcites →https://doi.org/10.1039/b709565copenalex-snapshot
Palladium and copper-catalysed arylation reactions in the presence of water, with a focus on carbon–heteroatom bond formation
inferredcites →https://doi.org/10.1039/b711523gopenalex-snapshot
Nucleophilic substitution of ferrocenyl alcohols “on water”
inferredcites →https://doi.org/10.1039/b719466hopenalex-snapshot
Direct arylations on water: synthesis of 2,5-disubstituted oxazoles balsoxin and texaline
inferredcites →https://doi.org/10.1055/s-1994-25562openalex-snapshot
Water-Promoted Organic Reactions
inferredcites →https://doi.org/10.1055/s-2008-1067086openalex-snapshot
Catalytic Strategies for Sustainable Oxidations in Water
inferredcites →https://doi.org/10.1070/rc2000v069n11abeh000609openalex-snapshot
Polynuclear complexes of copper(I) halides: coordination chemistry and catalytic transformations of alkynes
inferredcites →https://doi.org/10.1080/00397910600773684openalex-snapshot
One‐Pot Wittig Reactions in Aqueous Media: A Rapid and Environmentally Benign Synthesis of α,β‐Unsaturated Carboxylic Esters and Nitriles
inferredcites →https://doi.org/10.1126/science.1146421openalex-snapshot
Epoxide-Opening Cascades Promoted by Water
inferredcites →https://doi.org/10.1139/v06-150openalex-snapshot
Synthesis of β-hydroxy dithiocarbamate derivatives via regioselective addition of dithiocarbamate anion to epoxide in water
inferredcites →https://doi.org/10.1351/pac200577111807openalex-snapshot
Kinetics of electrophile-nucleophile combinations: A general approach to polar organic reactivity
inferredcites →https://doi.org/10.2174/1570178043488338openalex-snapshot
A One-Pot, Rhodium-Catalyzed Hydrostannylation-Conjugate Addition in Air and Water
inferredcites →https://doi.org/10.5860/choice.35-3311openalex-snapshot
Organic reactions in aqueous media
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Synthesis and Investigation of Photophysical Properties of Fluorescent Dyes Obtained by the Knoevenagel Condensation Reaction of Mono, Di or Tri Formyl Aromatic Aldehydes and Various Ch Acids
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Biphasic Catalysis—Homogeneous
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Organic Synthesis in Water
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Design and Evolution of Artificial Metalloenzymes: Biomimetic Aspects
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Diarylprolinol Silyl Ethers: Development and Application As Organocatalysts
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Oxidation of Alcohols Using Nanocatalysts
inferred← citeshttps://doi.org/10.1002/9781119870647.ch25openalex-snapshot
The Role of Water in Reactions Catalyzed by Transition Metals
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc2418openalex-snapshot
Sustainable Synthesis of Fine Chemicals from Aliphatic Nitro Compounds
inferred← citeshttps://doi.org/10.1002/9781119953678.rad074openalex-snapshot
Silanes as Reducing Reagents in Radical Chemistry
inferred← citeshttps://doi.org/10.1002/9783527641789.ch11openalex-snapshot
Adsorption Studies, Modeling, and Use of Green Inhibitors in Corrosion Inhibition: An Overview of Recent Research
inferred← citeshttps://doi.org/10.1002/9783527648283.ch7openalex-snapshot
Cross‐Coupling Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/9783527656790.ch1openalex-snapshot
Metal‐Catalyzed Cross‐Couplings of Aryl Halides to Form C–C Bonds in Aqueous Media
inferred← citeshttps://doi.org/10.1002/9783527656790.ch2openalex-snapshot
Metal‐Catalyzed C–H Bond Activation and C–C Bond Formation in Water
inferred← citeshttps://doi.org/10.1002/9783527664801.ch19openalex-snapshot
Synthetic Chemistry with an Eye on Future Sustainability
inferred← citeshttps://doi.org/10.1002/9783527805624.ch1openalex-snapshot
The Applications of Water as Reagents in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9783527805624.ch10openalex-snapshot
Alcohol as a Reagent in Homogeneous Catalysis
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz14077openalex-snapshot
reaction/catalysis “on water”
inferred← citeshttps://doi.org/10.1002/9783527814923.ch14openalex-snapshot
Supramolecular Catalysis in Water
inferred← citeshttps://doi.org/10.1002/9783527831463.ch1openalex-snapshot
Introduction: Scope of the Book
inferred← citeshttps://doi.org/10.1002/9783527834044.ch18openalex-snapshot
Aqueous Micellar Solutions in Photocatalysis
inferred← citeshttps://doi.org/10.1002/9783527846849.ch1openalex-snapshot
An Introduction to Organic Transformations in Water
inferred← citeshttps://doi.org/10.1002/9783527846849.ch10openalex-snapshot
Radical Reactions in Water
inferred← citeshttps://doi.org/10.1002/9783527846849.ch14openalex-snapshot
Organocatalytic Reactions in Water
inferred← citeshttps://doi.org/10.1002/9783527846849.ch17openalex-snapshot
Industrial Applications of Organic Reactions in Water
inferred← citeshttps://doi.org/10.1002/9783527846849.ch2openalex-snapshot
Chemistry of “On‐Water” Reactions
inferred← citeshttps://doi.org/10.1002/9783527846849.ch3openalex-snapshot
Chemistry of “In‐Water” Reactions: Spotlights on Micellar and Phase‐Transfer Catalysis
inferred← citeshttps://doi.org/10.1002/9783527846849.ch5openalex-snapshot
C–H Activation Reactions in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/9783527846849.ch7openalex-snapshot
Pericyclic Reactions in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/adsc.200900345openalex-snapshot
Insights into the Role of New Palladium Pincer Complexes as Robust and Recyclable Precatalysts for Suzuki–Miyaura Couplings in Neat Water
inferred← citeshttps://doi.org/10.1002/adsc.200900348openalex-snapshot
Hydroxypropyl‐α‐Cyclodextrin‐Capped Palladium Nanoparticles: Active Scaffolds for Efficient Carbon‐Carbon Bond Forming Cross‐Couplings in Water
inferred← citeshttps://doi.org/10.1002/adsc.200900765openalex-snapshot
Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji–Trost Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201000579openalex-snapshot
Efficient Palladium‐Catalyzed Double Arylation of Phosphonoalkynes and Diarylalkynes in Water: Use of a Dinuclear Palladium(I) Catalyst
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/adsc.201000868openalex-snapshot
Insights into Supported Copper(II)‐Catalyzed Azide‐Alkyne Cycloaddition in Water
inferred← citeshttps://doi.org/10.1002/adsc.201000962openalex-snapshot
N‐Alkylation of Amines with Alcohols Catalyzed by a Water‐Soluble Cp*Iridium Complex: An Efficient Method for the Synthesis of Amines in Aqueous Media
inferred← citeshttps://doi.org/10.1002/adsc.201100296openalex-snapshot
On‐Water Vinylogous Mukaiyama–Michael Addition of Heterocyclic 2‐Silyloxydienes to 1,2‐Diaza‐1,3‐dienes: One‐Pot Three‐Step Entry to Functionality‐Rich Pyrroles
inferred← citeshttps://doi.org/10.1002/adsc.201100449openalex-snapshot
The Efficient Copper(I) (Hexabenzyl)tren Catalyst and Dendritic Analogues for Green “Click” Reactions between Azides and Alkynes in Organic Solvent and in Water: Positive Dendritic Effects and Monometallic Mechanism
inferred← citeshttps://doi.org/10.1002/adsc.201100572openalex-snapshot
Aqueous and Solvent‐Free Uncatalyzed Three‐Component Vinylogous Mukaiyama–Mannich Reactions of Pyrrole‐Based Silyl Dienolates
inferred← citeshttps://doi.org/10.1002/adsc.201100788openalex-snapshot
A Highly Efficient Palladium‐Catalyzed One‐Pot Synthesis of Unsymmetrical Aryl Alkyl Thioethers under Mild Conditions in Water
inferred← citeshttps://doi.org/10.1002/adsc.201100835openalex-snapshot
Palladium‐Catalyzed, Highly Efficient, Regiocontrolled Arylation of Electron‐Rich Allylamines with Aryl Halides
inferred← citeshttps://doi.org/10.1002/adsc.201200448openalex-snapshot
Salt‐Controlled Selectivity in “on Water” and “in Water” Passerini‐Type Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201200856openalex-snapshot
Multifunctional “Click” Prolinamides: A New Platform for Asymmetric Aldol Reactions in the Presence of Water with Catalyst Recycling
inferred← citeshttps://doi.org/10.1002/adsc.201300711openalex-snapshot
The N‐Alkylation of Sulfonamides with Alcohols in Water Catalyzed by the Water‐Soluble Iridium Complex {Cp*Ir[6,6′‐(OH)2bpy](H2O)}[OTf]2
inferred← citeshttps://doi.org/10.1002/adsc.201300967openalex-snapshot
A Bis(Triazolecarboxamido) Ligand for Enantio‐ and Regioselective Molybdenum‐Catalyzed Asymmetric Allylic Alkylation Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201400785openalex-snapshot
Room‐Temperature Copper‐Catalyzed Arylation of Dimethylamine and Methylamine in Neat Water
inferred← citeshttps://doi.org/10.1002/adsc.201500358openalex-snapshot
Catalysis by β‐Cyclodextrin Hydrate – Synthesis of 2,2‐Disubstituted 2H‐Chromenes in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/adsc.201501132openalex-snapshot
Palladium Nanoparticles in Water: A Reusable Catalytic System for the Cycloetherification or Benzannulation of α‐Allenols
inferred← citeshttps://doi.org/10.1002/adsc.201600815openalex-snapshot
Ligand‐Free C–C Coupling Reactions Promoted by Hexagonal Boron Nitride‐Supported Palladium(II) Catalyst in Water
inferred← citeshttps://doi.org/10.1002/adsc.201701063openalex-snapshot
Water‐Mediated One‐pot Three‐Component Synthesis of Hydrazinyl‐Thiazoles Catalyzed by Copper Oxide Nanoparticles Dispersed on Titanium Dioxide Support: A Green Catalytic Process
inferred← citeshttps://doi.org/10.1002/adsc.201800743openalex-snapshot
Magnetic Nanoparticle Anchored Deep Eutectic Solvents as a Catalyst for the Etherification and Amination of Naphthols
inferred← citeshttps://doi.org/10.1002/adsc.201800749openalex-snapshot
Stereodiversified Modular Synthesis of Non‐planar Five‐Membered Cyclic N‐Hydroxylamidines: Reactivity Study and Application to the Synthesis of Cyclic Amidines
inferred← citeshttps://doi.org/10.1002/adsc.201900558openalex-snapshot
Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles
inferred← citeshttps://doi.org/10.1002/adsc.201901037openalex-snapshot
Alkylation of Indoles with α,β‐Unsaturated Ketones using Alumina in Hexanes
inferred← citeshttps://doi.org/10.1002/adsc.201901096openalex-snapshot
Amino Acids: Nontoxic and Cheap Alternatives for Amines for the Synthesis of Benzoxazoles through the Oxidative Functionalization of Catechols
inferred← citeshttps://doi.org/10.1002/adsc.201901536openalex-snapshot
Rongalite‐Promoted on Water Synthesis of Functionalised Tellurides and Ditellurides
inferred← citeshttps://doi.org/10.1002/adsc.202000020openalex-snapshot
DBSA‐Catalyzed Regioselective Dehydrative Friedel‐Crafts Arylation of CF3‐Containing 3‐Indolyl(2‐thiophenyl)methanols with 2‐Substituted Indoles in Water
inferred← citeshttps://doi.org/10.1002/adsc.202001358openalex-snapshot
Recent Advances in Cross‐Dehydrogenative Couplings (CDC) of C−H Bond in Aqueous Media
inferred← citeshttps://doi.org/10.1002/adsc.202001407openalex-snapshot
Recent Trends and Prospects in the Copper‐Catalysed “on Water” Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202100535openalex-snapshot
Direct Use of Benzylic Alcohols for Multicomponent Synthesis of 2‐Aryl Quinazolinones Utilizing the π‐Benzylpalladium(II) System in Water
inferred← citeshttps://doi.org/10.1002/adsc.202200486openalex-snapshot
4‐(Dimethylamino)Pyridinium Azide in Protic Ionic Liquid Media as a Stable Equivalent of Hydrazoic Acid
inferred← citeshttps://doi.org/10.1002/adsc.202300947openalex-snapshot
Pentafluorophenyl‐Substituted Proline‐Derived Chiral Urea for “On Water” Asymmetric Hydrogen‐Bonding Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.202400298openalex-snapshot
On‐off Pulsed Ultrasound Promote Asymmetric Noncovalent Organocatalysis “on Water”: An Investigation in Michael Addition and Diels‐Alder Reactions
inferred← citeshttps://doi.org/10.1002/aic.18038openalex-snapshot
Catalytic template assisted interfacial polymerization for high‐performance acid‐resistant membrane preparation
inferred← citeshttps://doi.org/10.1002/aic.70162openalex-snapshot
Highly permeable organic solvent nanofiltration membrane prepared via cosolvent‐assisted interfacial polymerization
inferred← citeshttps://doi.org/10.1002/ajoc.201500397openalex-snapshot
p‐Toluenesulfonic Acid‐Mediated Three‐Component Reaction “On‐Water” Protocol for the Synthesis of Novel Thiadiazolo[2,3‐b]quinazolin‐6(7H)‐ones
inferred← citeshttps://doi.org/10.1002/ajoc.201600346openalex-snapshot
Catalyst‐Free Synthesis of 3‐Aryl‐3‐hydroxy‐2‐oxindole Derivatives by Using Water as the Solvent: Experimental and DFT Studies
inferred← citeshttps://doi.org/10.1002/ajoc.201600384openalex-snapshot
Designing Vasicine‐Derived Ligands and Their Application for Ruthenium‐Catalyzed Transfer Hydrogenation Reactions in Water: Synthesis of Amines and Alcohols
inferred← citeshttps://doi.org/10.1002/ajoc.201600475openalex-snapshot
Highly Efficient Brønsted Acidic Ionic Liquid Promoted Direct Diazenylation of Pyrazolones with Aryltriazenes under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ajoc.201700618openalex-snapshot
Palladium‐Catalyzed Dehydrogenation of Benzyl Alcohols for Construction of 2‐Arylbenzimidazoles “On Water”
inferred← citeshttps://doi.org/10.1002/ajoc.201700670openalex-snapshot
Catalyst‐Free Regioselective Sulfenylation of Imidazoheterocycles with Sulfonyl Hydrazides in Water
inferred← citeshttps://doi.org/10.1002/ajoc.201800396openalex-snapshot
Synthesis of Biologically Relevant Heterocycles in Aqueous Media
inferred← citeshttps://doi.org/10.1002/ajoc.202000419openalex-snapshot
Proline‐derived Long‐aliphatic‐chain Amphiphilic Organocatalysts (PDLACAOs) for Asymmetric Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/ajoc.202100308openalex-snapshot
Visible‐Light Mediated Metal‐Free Cross‐Electrophile Coupling of Isatin Derivatives with Electron‐Poor Alkenes
inferred← citeshttps://doi.org/10.1002/ajoc.202100427openalex-snapshot
Recent Advances in Metal‐ and Organocatalyzed Asymmetric Functionalization of Pyrroles
inferred← citeshttps://doi.org/10.1002/ajoc.202100773openalex-snapshot
Copper Sulfate‐Catalyzed Asymmetric 1,4‐Addition of Amido‐Functionalized Allylboronates to Maleimides in Water
inferred← citeshttps://doi.org/10.1002/ajoc.202200125openalex-snapshot
Aqueous Mediated Reactions Involving Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1002/ajoc.202200331openalex-snapshot
Transition‐metal‐catalyzed Heteroannulation Reactions in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/ajoc.202300071openalex-snapshot
Pd‐Catalyzed Dehydrative Synthesis of Allylic Amines in Water
inferred← citeshttps://doi.org/10.1002/ajoc.202300159openalex-snapshot
I2‐Mediated Oxidation of Amines in Water toward Imines and Amides
inferred← citeshttps://doi.org/10.1002/ajoc.202400812openalex-snapshot
Synthesis of Chiral β‐Trifluoromethyl‐β‐Amino Acid Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/ange.200902570openalex-snapshot
pH‐Regulated Asymmetric Transfer Hydrogenation of Quinolines in Water
inferred← citeshttps://doi.org/10.1002/ange.200905626openalex-snapshot
A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/ange.201200390openalex-snapshot
Rhodium(I)‐Catalyzed Domino Asymmetric Ring Opening/Enantioselective Isomerization of Oxabicyclic Alkenes with Water
inferred← citeshttps://doi.org/10.1002/ange.201200575openalex-snapshot
Investigation of “On Water” Conditions Using a Biphasic Fluidic Platform
inferred← citeshttps://doi.org/10.1002/ange.201208741openalex-snapshot
Lichtinduzierte Klickreaktionen
inferred← citeshttps://doi.org/10.1002/ange.201306632openalex-snapshot
Surfactant‐Type Brønsted Acid Catalyzed Stereoselective Synthesis of trans‐3‐Alkenyl Indazoles from Triazenylaryl Allylic Alcohols in Water
inferred← citeshttps://doi.org/10.1002/ange.201510090openalex-snapshot
Direct Observation of Self‐Organized Water‐Containing Structures in the Liquid Phase and Their Influence on 5‐(Hydroxymethyl)furfural Formation in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/ange.201511348openalex-snapshot
Chemoreactive Natural Products that Afford Resistance Against Disparate Antibiotics and Toxins
inferred← citeshttps://doi.org/10.1002/ange.201705006openalex-snapshot
Ruthenium‐Catalyzed Azide–Thioalkyne Cycloadditions in Aqueous Media: A Mild, Orthogonal, and Biocompatible Chemical Ligation
inferred← citeshttps://doi.org/10.1002/ange.201705412openalex-snapshot
Unprecedented Nucleophilic Additions of Highly Polar Organometallic Compounds to Imines and Nitriles Using Water as a Non‐Innocent Reaction Medium
inferred← citeshttps://doi.org/10.1002/ange.201708413openalex-snapshot
“On‐Droplet” Chemistry: The Cycloaddition of Diethyl Azodicarboxylate and Quadricyclane
inferred← citeshttps://doi.org/10.1002/ange.201809100openalex-snapshot
“On Water” Surface‐initiated Polymerization of Hydrophobic Monomers
inferred← citeshttps://doi.org/10.1002/ange.201812537openalex-snapshot
Water and Sodium Chloride: Essential Ingredients for Robust and Fast Pd‐Catalysed Cross‐Coupling Reactions between Organolithium Reagents and (Hetero)aryl Halides
inferred← citeshttps://doi.org/10.1002/ange.202003948openalex-snapshot
Cycloisomerization of Olefins in Water
inferred← citeshttps://doi.org/10.1002/ange.202103555openalex-snapshot
Interfacial Polymerization at the Alkane/Ionic Liquid Interface
inferred← citeshttps://doi.org/10.1002/ange.202103645openalex-snapshot
Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes
inferred← citeshttps://doi.org/10.1002/ange.202304720openalex-snapshot
Introducing Water and Deep Eutectic Solvents in Organosodium Chemistry: Chemoselective Nucleophilic Functionalizations in Air
inferred← citeshttps://doi.org/10.1002/ange.202518462openalex-snapshot
Where's the Salt? Sensing the Ionic Environment of the Air–Organic–Water Interface Using an Azide Probe
inferred← citeshttps://doi.org/10.1002/ange.5126293openalex-snapshot
Recyclable Pt‐Catalyzed Biphase Hydrosilylation on Water: From Functionalized Monomers to Polymer Materials
inferred← citeshttps://doi.org/10.1002/ange.9297515openalex-snapshot
Sustainable Pd‐Catalyzed Aminations “on Dirty Water”
inferred← citeshttps://doi.org/10.1002/anie.200902570openalex-snapshot
pH‐Regulated Asymmetric Transfer Hydrogenation of Quinolines in Water
inferred← citeshttps://doi.org/10.1002/anie.200905626openalex-snapshot
A Practical Heterogeneous Catalyst for the Suzuki, Sonogashira, and Stille Coupling Reactions of Unreactive Aryl Chlorides
inferred← citeshttps://doi.org/10.1002/anie.201200390openalex-snapshot
Rhodium(I)‐Catalyzed Domino Asymmetric Ring Opening/Enantioselective Isomerization of Oxabicyclic Alkenes with Water
inferred← citeshttps://doi.org/10.1002/anie.201200575openalex-snapshot
Investigation of “On Water” Conditions Using a Biphasic Fluidic Platform
inferred← citeshttps://doi.org/10.1002/anie.201306632openalex-snapshot
Surfactant‐Type Brønsted Acid Catalyzed Stereoselective Synthesis of trans‐3‐Alkenyl Indazoles from Triazenylaryl Allylic Alcohols in Water
inferred← citeshttps://doi.org/10.1002/anie.201510090openalex-snapshot
Direct Observation of Self‐Organized Water‐Containing Structures in the Liquid Phase and Their Influence on 5‐(Hydroxymethyl)furfural Formation in Ionic Liquids
inferred← citeshttps://doi.org/10.1002/anie.201511348openalex-snapshot
Chemoreactive Natural Products that Afford Resistance Against Disparate Antibiotics and Toxins
inferred← citeshttps://doi.org/10.1002/anie.201705006openalex-snapshot
Ruthenium‐Catalyzed Azide–Thioalkyne Cycloadditions in Aqueous Media: A Mild, Orthogonal, and Biocompatible Chemical Ligation
inferred← citeshttps://doi.org/10.1002/anie.201705412openalex-snapshot
Unprecedented Nucleophilic Additions of Highly Polar Organometallic Compounds to Imines and Nitriles Using Water as a Non‐Innocent Reaction Medium
inferred← citeshttps://doi.org/10.1002/anie.201708413openalex-snapshot
“On‐Droplet” Chemistry: The Cycloaddition of Diethyl Azodicarboxylate and Quadricyclane
inferred← citeshttps://doi.org/10.1002/anie.201809100openalex-snapshot
“On Water” Surface‐initiated Polymerization of Hydrophobic Monomers
inferred← citeshttps://doi.org/10.1002/anie.201812537openalex-snapshot
Water and Sodium Chloride: Essential Ingredients for Robust and Fast Pd‐Catalysed Cross‐Coupling Reactions between Organolithium Reagents and (Hetero)aryl Halides
inferred← citeshttps://doi.org/10.1002/anie.202003948openalex-snapshot
Cycloisomerization of Olefins in Water
inferred← citeshttps://doi.org/10.1002/anie.202103555openalex-snapshot
Interfacial Polymerization at the Alkane/Ionic Liquid Interface
inferred← citeshttps://doi.org/10.1002/anie.202103645openalex-snapshot
Bioorthogonal Azide–Thioalkyne Cycloaddition Catalyzed by Photoactivatable Ruthenium(II) Complexes
inferred← citeshttps://doi.org/10.1002/anie.202304720openalex-snapshot
Introducing Water and Deep Eutectic Solvents in Organosodium Chemistry: Chemoselective Nucleophilic Functionalizations in Air
inferred← citeshttps://doi.org/10.1002/anie.202518462openalex-snapshot
Where's the Salt? Sensing the Ionic Environment of the Air–Organic–Water Interface Using an Azide Probe
inferred← citeshttps://doi.org/10.1002/anie.5126293openalex-snapshot
Recyclable Pt‐Catalyzed Biphase Hydrosilylation on Water: From Functionalized Monomers to Polymer Materials
inferred← citeshttps://doi.org/10.1002/anie.9297515openalex-snapshot
Sustainable Pd‐Catalyzed Aminations “on Dirty Water”
inferred← citeshttps://doi.org/10.1002/aoc.1824openalex-snapshot
Synthesis of water‐soluble monotosylated ethylenediamines and their application in ruthenium and iridium‐catalyzed transfer hydrogenation of aldehydes
inferred← citeshttps://doi.org/10.1002/aoc.1857openalex-snapshot
A PdCl2–ionic liquid brush assembly: an efficient and reusable catalyst for Mizoroki–Heck reaction in neat water
inferred← citeshttps://doi.org/10.1002/aoc.1867openalex-snapshot
Nucleophilic substitution of ferrocenyl alcohols catalyzed by bismuth(III) in aqueous medium at room temperature
inferred← citeshttps://doi.org/10.1002/aoc.2895openalex-snapshot
Zn[(L)Proline]2: an eligible candidate for the synthesis of xanthenediones in water
inferred← citeshttps://doi.org/10.1002/aoc.2957openalex-snapshot
Basic CuCO3/ligand as a new catalyst for 'on water' borylation of Michael acceptors, alkenes and alkynes: application to the efficient asymmetric synthesis of β‐alcohol type sitagliptin side chain
inferred← citeshttps://doi.org/10.1002/aoc.3129openalex-snapshot
Pd( l ‐proline)2complex: an efficient catalyst for Suzuki–Miyaura coupling reaction in neat water
inferred← citeshttps://doi.org/10.1002/aoc.3392openalex-snapshot
A new magnetically recoverable heterogeneous palladium catalyst for phosphonation reactions in aqueous micellar solution
inferred← citeshttps://doi.org/10.1002/aoc.3471openalex-snapshot
Highly efficient and reusable polystyrene‐supported copper(II) catalytic system for S‐arylation of potassium thiocyanate by aryl halides in water
inferred← citeshttps://doi.org/10.1002/aoc.3473openalex-snapshot
Highly selective copper‐catalyzed oxidation of benzyl alcohols to aromatic aldehydes in water at room temperature
inferred← citeshttps://doi.org/10.1002/aoc.3536openalex-snapshot
A robust synthesis and characterization of superparamagnetic CoFe2O4 nanoparticles as an efficient and reusable catalyst for green synthesis of some heterocyclic rings
inferred← citeshttps://doi.org/10.1002/aoc.3598openalex-snapshot
Fe3O4@TiO2@O2PO2(CH2)NHSO3H as a novel nanomagnetic catalyst: Application to the preparation of 2‐amino‐4,6‐diphenylnicotinonitriles via anomeric‐based oxidation
inferred← citeshttps://doi.org/10.1002/aoc.3816openalex-snapshot
Synthesis of pyrano[2,3‐c]pyrazole derivatives using Fe3O4@SiO2@piperidinium benzene‐1,3‐disulfonate (Fe3O4@SiO2 nanoparticle‐supported IL) as a novel, green and heterogeneous catalyst
inferred← citeshttps://doi.org/10.1002/aoc.4063openalex-snapshot
Catalytic application of sulfonic acid‐functionalized titana‐coated magnetic nanoparticles for the preparation of 1,8‐dioxodecahydroacridines and 2,4,6‐triarylpyridines via anomeric‐based oxidation
inferred← citeshttps://doi.org/10.1002/aoc.4203openalex-snapshot
Denitrogenative Pd/Cu‐catalyzed Suzuki‐type Cross‐coupling of Aryltrifluoroborates with Arylhydrazine Hydrochlorides in Water under Room Temperature
inferred← citeshttps://doi.org/10.1002/aoc.4227openalex-snapshot
Use of an efficient polystyrene‐supported cerium catalyst for one‐pot multicomponent synthesis of spiro‐piperidine derivatives and click reactions in green solvent
inferred← citeshttps://doi.org/10.1002/aoc.4421openalex-snapshot
Urea‐based amphiphilic porous organic polymer‐supported palladium as a reusable catalyst for Suzuki–Miyaura coupling and hydroxycarbonylation reactions in water
inferred← citeshttps://doi.org/10.1002/aoc.4479openalex-snapshot
H 5 BW 12 O 40 as a green and efficient homogeneous but recyclable catalyst in the synthesis of 4 H ‐Pyrans via multicomponent reaction
inferred← citeshttps://doi.org/10.1002/aoc.4989openalex-snapshot
Iron (III)‐porphyrin Complex FeTSPP as an efficient catalyst for synthesis of tetrazole derivatives via [2 + 3]cycloaddition reaction in aqueous medium
inferred← citeshttps://doi.org/10.1002/aoc.5226openalex-snapshot
Oxime‐derived palladacycle Immobilized in an Ionic Liquid Brush as an Efficient and Reusable Catalyst for Mozoroki‐Heck Reaction in Neat Water
inferred← citeshttps://doi.org/10.1002/aoc.5289openalex-snapshot
Half‐sandwich ruthenium complexes with S chiff base ligands bearing a hydroxyl group: Preparation, characterization and catalytic activities
inferred← citeshttps://doi.org/10.1002/aoc.5513openalex-snapshot
Palladium‐catalyzed cyclization reaction of N‐(2‐Haloaryl)alkynylimines: Synthesis of 3‐acylindoles using water as the sole solvent and oxygen source
inferred← citeshttps://doi.org/10.1002/aoc.6223openalex-snapshot
Cu(OAc)2‐porphyrins as an efficient catalytic system for base‐free, nature mimicking Chan–Lam coupling in water
inferred← citeshttps://doi.org/10.1002/aoc.6418openalex-snapshot
Indium‐mediated allylation of carbonyl compounds in deep eutectic solvents
inferred← citeshttps://doi.org/10.1002/aoc.70012openalex-snapshot
Highly Efficient Ag/Fe3O4@MWCNTs MNCs Catalyzed Green Synthesis of New Derivatives of 1,2,4‐Triazine: The Cytotoxic Activity Investigation of 1,2,4‐Triazines
inferred← citeshttps://doi.org/10.1002/aoc.70164openalex-snapshot
Ag/SiO2/Fe3O4@GO as a Recyclable Catalyst Promoted Green Synthesis of Novel Pyrimidoazepines via Multicomponent Reaction of Isatins Employing
inferred← citeshttps://doi.org/10.1002/aoc.70168openalex-snapshot
Green Synthesis of New Chromenopyridines as New Heterocyclic Compounds and Evaluation of Biological Activity Using ZnO/Fe3O4 Decorated on Graphene Oxide
inferred← citeshttps://doi.org/10.1002/aoc.70302openalex-snapshot
Green Synthesis of Thiazinoquinolines and Evaluation of Antimicrobial and Antioxidant Activity Employing ZnO/CuO@GO Organometallic Nanocatalyst
inferred← citeshttps://doi.org/10.1002/aoc.70376openalex-snapshot
Green Synthesis of Novel Cyclopenta[1,2‐d]pyrimidins Using Ag/Fe3O4@GO Nanocatalyst: Characterization and Biological Activity
inferred← citeshttps://doi.org/10.1002/aoc.70592openalex-snapshot
Click Chemistry by Mes‐Imd Tagged Copper Catalysts for the Synthesis of 1,4‐Disubstituted 1,2,3‐Triazoles and 5‐Substituted 1H‐Tetrazoles in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/aoc.7252openalex-snapshot
Green synthesis and theoretical study of new 1,3,4‐oxadiazoles: Application of Cu/Fe3O4@MWCNT magnetic nanocomposites
inferred← citeshttps://doi.org/10.1002/aoc.7691openalex-snapshot
Employing Cu@Fe3O4/SiO2@MWCNTs as New Catalyst for the Green Synthesis of New Pyridopyrroloindoles Using Multicomponent Reactions of Isatins
inferred← citeshttps://doi.org/10.1002/aoc.7718openalex-snapshot
One‐Pot Multicomponent Synthesis of Substituted 1,6‐Naphthyridine Derivatives Employing 4‐Aminocumarin
inferred← citeshttps://doi.org/10.1002/aoc.7787openalex-snapshot
Bio‐Ag/ZnO@MWCNTs Promoted Green Synthesis of Novel Bis‐Pyrimidothiazines: Evaluation of Biological Activity
inferred← citeshttps://doi.org/10.1002/aoc.7855openalex-snapshot
Green Synthesis and Biological Study of Novel Cyclopenta[b]pyrrolizine: One‐Pot Multicomponent Reactions via Ag/Fe3O4@MWCNTs
inferred← citeshttps://doi.org/10.1002/aoc.7888openalex-snapshot
Green Synthesis of New Coumarins Employing SiO2/Fe3O4@MWCNTs as a Recyclable Catalyst and Evaluation of Antioxidant and Antiproliferative Activity
inferred← citeshttps://doi.org/10.1002/asia.201000071openalex-snapshot
Triazole‐Functionalized N‐Heterocyclic Carbene Complexes of Palladium and Platinum and Efficient Aqueous Suzuki–Miyaura Coupling Reaction
inferred← citeshttps://doi.org/10.1002/asia.201100174openalex-snapshot
“On Water” Nucleophilic Addition of Formaldehyde N,N‐Dialkylhydrazones to α‐Keto Esters
inferred← citeshttps://doi.org/10.1002/asia.201300440openalex-snapshot
Allylation Reactions of Aldehydes with Allylboronates in Aqueous Media: Unique Reactivity and Selectivity that are Only Observed in the Presence of Water
inferred← citeshttps://doi.org/10.1002/asia.201600744openalex-snapshot
Improvement in Aqueous Solubility of Retinoic Acid Receptor (RAR) Agonists by Bending the Molecular Structure
inferred← citeshttps://doi.org/10.1002/asia.201800358openalex-snapshot
An Active Palladium Colloidal Catalyst for the Selective Oxidative Heterocoupling of (Hetero)Aryl Boronic Acids
inferred← citeshttps://doi.org/10.1002/asia.201900982openalex-snapshot
Micelle‐Enabled One‐Pot Guanidine Synthesis in Water Directly from Isothiocyanate using Hypervalent Iodine(III) Reagents under Mild Conditions
inferred← citeshttps://doi.org/10.1002/asia.202100321openalex-snapshot
Rhodium‐terpyridine Catalyzed Transfer Hydrogenation of Aromatic Nitro Compounds in Water
inferred← citeshttps://doi.org/10.1002/asia.202100920openalex-snapshot
π‐Face Promoted Catalysis in Water: From Electron‐deficient Molecular Cages to Single Aromatic Slides
inferred← citeshttps://doi.org/10.1002/asia.202200883openalex-snapshot
Acceptorless Dehydrogenation of Alcohols and Transfer Hydrogenation of Aldehydes in Water Using a Single Bifunctional, Bistate, Water‐soluble Ruthenium Catalyst
inferred← citeshttps://doi.org/10.1002/asia.202300815openalex-snapshot
Transition‐Metal‐Catalyzed Directed C−H Functionalization in/on Water
inferred← citeshttps://doi.org/10.1002/asia.202500113openalex-snapshot
The Synergy of Microwave‐Irradiation and Water Surface: A Fast Access to C‐2 Functionalized Indolizines Via Baylis–Hillman Reaction
inferred← citeshttps://doi.org/10.1002/asia.70471openalex-snapshot
Recent Advances in Transition Metal–Catalyzed Csp 2 ‐X (X = S, N, O) Cross‐Coupling Reactions in Water
inferred← citeshttps://doi.org/10.1002/bkcs.10434openalex-snapshot
Facile Synthesis of Glycidyl Triazolyl Polymers in Water Using β‐Cyclodextrin
inferred← citeshttps://doi.org/10.1002/bkcs.70127openalex-snapshot
Research on synthesis of microwave‐assisted heterocyclic compounds with eco‐friendly solvents and transition metals via C–H activation
inferred← citeshttps://doi.org/10.1002/cctc.200900256openalex-snapshot
Ionic Tags in Catalyst Optimization: Beyond Catalyst Recycling
inferred← citeshttps://doi.org/10.1002/cctc.201000437openalex-snapshot
Dual Catalysis in Highly Enantioselective Multicomponent Reaction with Water: An Efficient Approach to Chiral β‐Amino‐α‐Hydroxy Acid Derivatives
inferred← citeshttps://doi.org/10.1002/cctc.201300339openalex-snapshot
Polymer‐ and Ionic Liquid‐Containing Palladium: Recoverable Soluble Cross‐Coupling Catalysts
inferred← citeshttps://doi.org/10.1002/cctc.201300458openalex-snapshot
1,2,3‐Trimethoxypropane and Glycerol Ethers as Bio‐Sourced Solvents from Glycerol. Synthesis by Solvent‐Free Phase‐Transfer Catalysis and Utilization as an Alternative Solvent in Chemical Transformations
inferred← citeshttps://doi.org/10.1002/cctc.201300870openalex-snapshot
Modulation of Silver–Titania Nanoparticles on Polymethylhydrosiloxane‐based Semi‐Interpenetrating Networks for Catalytic Alkynylation of Trifluoromethyl Ketones and Aromatic Aldehydes in Water
inferred← citeshttps://doi.org/10.1002/cctc.201402176openalex-snapshot
CuII and Cu0 Catalyzed Mono Borylation of Unsaturated Hydrocarbons with B2pin2: Entering into the Water
inferred← citeshttps://doi.org/10.1002/cctc.201601522openalex-snapshot
Role of Water in Catalyzing Proton Transfer in Glucose Dehydration to 5‐Hydroxymethylfurfural
inferred← citeshttps://doi.org/10.1002/cctc.202400723openalex-snapshot
From Aldehyde to Ketone via Water‐Accelerated Molybdenum‐Photocatalysis
inferred← citeshttps://doi.org/10.1002/cctc.202401825openalex-snapshot
Pd/CeO2 Single‐Atom Catalyst Forms Atypical C4 Product in a Suzuki Reaction with 2,4‐Dibromopyridine
inferred← citeshttps://doi.org/10.1002/cctc.202501441openalex-snapshot
Efficient Aqueous Intramolecular Alkyne Hydrofunctionalization Catalyzed by Monodentate Gold(I) Complex of Cocarboxylase
inferred← citeshttps://doi.org/10.1002/chem.200902252openalex-snapshot
Byproduct‐Catalyzed Four‐Component Reactions of Aldehydes with Hexamethyldisilazane, Chloroformates, and Nucleophiles in Acetonitrile Leading to Protected Primary Amines, β‐Amino Esters, and β‐Amino Ketones
inferred← citeshttps://doi.org/10.1002/chem.201000753openalex-snapshot
“On‐Water,” Microwave‐Assisted, Pd‐Catalyzed Synthesis of Indoles from Imines and o‐Difunctionalized Arenes
inferred← citeshttps://doi.org/10.1002/chem.201001387openalex-snapshot
Room‐Temperature Deoxygenation of Epoxides with CO Catalyzed by Hydrotalcite‐Supported Gold Nanoparticles in Water
inferred← citeshttps://doi.org/10.1002/chem.201001598openalex-snapshot
Electrophilic Reactivities of Azodicarboxylates
inferred← citeshttps://doi.org/10.1002/chem.201001705openalex-snapshot
The Mechanism of On‐Water Catalysis
inferred← citeshttps://doi.org/10.1002/chem.201101077openalex-snapshot
Asymmetric Mannich Reaction of Imines Derived from Aliphatic and Aromatic Aldehydes Catalyzed by Diarylprolinol Silyl Ether
inferred← citeshttps://doi.org/10.1002/chem.201102264openalex-snapshot
Acid–Base‐Catalysed Condensation Reaction in Water: Isoxazolines and Isoxazoles from Nitroacetates and Dipolarophiles
inferred← citeshttps://doi.org/10.1002/chem.201200049openalex-snapshot
Emulsion Reactors: A New Technique for the Preparation of Molecular Imaging Probes
inferred← citeshttps://doi.org/10.1002/chem.201201266openalex-snapshot
Suzuki Coupling Reactions in Neat Water as the Solvent: Where in the Biphasic Reaction Mixture Do the Catalytic Reaction Steps Occur?
inferred← citeshttps://doi.org/10.1002/chem.201202698openalex-snapshot
Conjugate Addition versus Cycloaddition/Condensation of Nitro Compounds in Water: Selectivity, Acid–Base Catalysis, and Induction Period
inferred← citeshttps://doi.org/10.1002/chem.201202886openalex-snapshot
Hot Water‐Promoted SN1 Solvolysis Reactions of Allylic and Benzylic Alcohols
inferred← citeshttps://doi.org/10.1002/chem.201204194openalex-snapshot
Fast Reductive Amination by Transfer Hydrogenation “on Water”
inferred← citeshttps://doi.org/10.1002/chem.201204373openalex-snapshot
Asymmetric Synthesis of trans‐β‐Lactams by a Kinugasa Reaction on Water
inferred← citeshttps://doi.org/10.1002/chem.201204396openalex-snapshot
The Combined Role of Catalysis and Solvent Effects on the Biginelli Reaction: Improving Efficiency and Sustainability
inferred← citeshttps://doi.org/10.1002/chem.201302838openalex-snapshot
“On Water”, Phosphine‐Free Palladium‐Catalyzed Room Temperature CH Arylation of Indoles
inferred← citeshttps://doi.org/10.1002/chem.201303069openalex-snapshot
Water Compatible Multicomponent Cascade Suzuki/Heck–Aldol, Suzuki–Aldol–Suzuki, and Aldol–Suzuki–Aldol Reactions: An Ecofriendly Paradigm for Multiple CarbonCarbon Bond Formation in One Pot
inferred← citeshttps://doi.org/10.1002/chem.201700832openalex-snapshot
Efficient and Mild Ullmann‐Type N‐Arylation of Amides, Carbamates, and Azoles in Water
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