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Reaction Solvent Selection: The Potential of Water as a Solvent for Organic Transformations

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Diels_Alder reactions in water

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INTRODUCTION
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A novel approach for selective cross aldol condensation using reusable NaOH-cationic micellar systems
inferred← citeshttps://doi.org/10.1016/j.apcata.2013.09.016openalex-snapshot
H40-PCL-PEG unimolecular micelles both as anchoring sites for palladium nanoparticles and micellar catalyst for Heck reaction in water
inferred← citeshttps://doi.org/10.1016/j.apsusc.2024.160198openalex-snapshot
Synthesis of InZrOx nanosheets and its application in CO2 hydrogenation to methanol
inferred← citeshttps://doi.org/10.1016/j.arabjc.2015.08.027openalex-snapshot
Aqua mediated multicomponent reaction under phase transfer catalysis: A novel and green approach to access fused pyrazoles
inferred← citeshttps://doi.org/10.1016/j.catcom.2009.12.005openalex-snapshot
Immobilization of β-cyclodextrin onto Dowex resin as a stationary microvessel and phase transfer catalyst
inferred← citeshttps://doi.org/10.1016/j.catcom.2011.02.027openalex-snapshot
Selective hydrogenation of nitroarenes using gum acacia supported Pt colloid an effective reusable catalyst in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.catcom.2015.06.005openalex-snapshot
Synthesis of atropisomeric chiral MeOBIPHEP analogues via Pd-catalyzed P–C coupling — applications to asymmetric Rh-catalyzed C–C bond formations in water
inferred← citeshttps://doi.org/10.1016/j.cattod.2011.01.050openalex-snapshot
Hydrogenation of bisphenol A – Using a mesoporous silica based nano ruthenium catalyst Ru/MCM-41 and water as the solvent
inferred← citeshttps://doi.org/10.1016/j.cattod.2018.11.044openalex-snapshot
A novel and an eco-friendly approach for organic dyes degradation using Spirulina platensis cultivated water
inferred← citeshttps://doi.org/10.1016/j.cclet.2008.07.016openalex-snapshot
Clean heterocyclic synthesis in water: I2/KI catalyzed one-pot synthesis of quinazolin-4(3H)-ones
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.04.033openalex-snapshot
Sustainable routes for quantitative green selenocyanation of activated alkynes
inferred← citeshttps://doi.org/10.1016/j.ccr.2024.216382openalex-snapshot
Recent trends and perspectives in rhenium-based nanomaterials for sustainable applications
inferred← citeshttps://doi.org/10.1016/j.cogsc.2022.100690openalex-snapshot
Efficient catalysis in dynamic nanomicelles of PS-750-M suspended in water
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2024.133368openalex-snapshot
Efficient hydrogenation of rosin and α-pinene catalyzed by amphiphilic Ni–W–B catalysts
inferred← citeshttps://doi.org/10.1016/j.crci.2018.03.010openalex-snapshot
Some aspects of green solvents
inferred← citeshttps://doi.org/10.1016/j.ica.2016.06.004openalex-snapshot
Micellar promoted alkenes isomerization in water mediated by a cationic half-sandwich Ru(II) complex
inferred← citeshttps://doi.org/10.1016/j.ica.2018.04.018openalex-snapshot
Palladium PEPPSI complexes: Synthesis and catalytic activity on the Suzuki-Miyaura coupling reactions for aryl bromides at room temperature in aqueous media
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115140openalex-snapshot
Aqueous-phase hydrogenation of α-pinene catalyzed by Ni-B alloys loaded on a Janus amphiphilic carbon@silica nanomaterial
inferred← citeshttps://doi.org/10.1016/j.jcat.2012.04.020openalex-snapshot
Deactivation of Ni/TiO2 catalyst in the hydrogenation of nitrobenzene in water and improvement in its stability by coating a layer of hydrophobic carbon
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122303openalex-snapshot
Directing group enabled ‘On-Water’ C H bond functionalization of ferrocene derivatives
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2008.03.007openalex-snapshot
Comparative effect of cyclodextrin nanocavities versus organic solvents on the fluorescence of carbamate and indole compounds
inferred← citeshttps://doi.org/10.1016/j.jscs.2014.04.001openalex-snapshot
One pot four component sequential synthesis of hexahydroquinoline derivatives in aqueous media via enaminone intermediates: A green protocol
inferred← citeshttps://doi.org/10.1016/j.micromeso.2017.04.048openalex-snapshot
Catecholase activity of a manganese Schiff base complex functionalized over SBA-15 in aqueous heterogeneous medium
inferred← citeshttps://doi.org/10.1016/j.molcata.2011.09.013openalex-snapshot
Disproportionation of hydrophobic dihydroarenes by recyclable rhodium and palladium catalysts in aqueous microemulsions
inferred← citeshttps://doi.org/10.1016/j.molliq.2015.02.017openalex-snapshot
Study on catalytic property of NaOH-cationic surfactant solutions for efficient, green and selective synthesis of flavanone
inferred← citeshttps://doi.org/10.1016/j.molliq.2019.112429openalex-snapshot
Micellar catalyzed hydroxylation of 1,2,3-trichloro-4,6-dinitrobenzene: Role of cationic head group–π interaction
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120817openalex-snapshot
Synergistic reinforcement of CPC/TX-100 mixed micellar microenvironment for diperiodatocuprate(III) (DPC) oxidation of 1-propanol and 1,3-propanediol
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116124openalex-snapshot
A retrospective-prospective review of Suzuki–Miyaura reaction: From cross-coupling reaction to pharmaceutical industry applications
inferred← citeshttps://doi.org/10.1016/j.scp.2018.06.001openalex-snapshot
Liquefied dimethyl ether (DME) as a green solvent in chemical reactions: Synthesis of O -alkyl trichloroacetimidates
inferred← citeshttps://doi.org/10.1016/j.seppur.2019.116403openalex-snapshot
High efficiency treatment of organic/inorganic pollutants using recyclable magnetic N-heterocyclic copper(II) complex and its antimicrobial applications
inferred← citeshttps://doi.org/10.1016/j.snr.2022.100100openalex-snapshot
A review on chemiresistive ZnO gas sensors
inferred← citeshttps://doi.org/10.1016/j.supflu.2016.02.012openalex-snapshot
Guide to by-products formed in organic solvents under solvothermal conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.03.034openalex-snapshot
Environmentally benign electrophilic and radical bromination ‘on water’: H2O2–HBr system versus N-bromosuccinimide
inferred← citeshttps://doi.org/10.1016/j.tet.2010.05.082openalex-snapshot
DBU: a highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H benzo[g]chromenes in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.020openalex-snapshot
New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4-b]pyridine derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.030openalex-snapshot
Urotropine–bromine promoted synthesis of functionalized oxaspirotricyclic furopyrimidines via a domino Knoevenagel condensation/Michael addition/α-bromination/Williamson cycloetherification sequence in water
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.005openalex-snapshot
Highly efficient heterogeneous synthesis of benzofurans under aqueous condition
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.077openalex-snapshot
Water as an additive for selective synthesis of saturated 1,4-diketones and tetrasubstituted furans directly from 1,4-enediones
inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.089openalex-snapshot
Synthesis of spiroindolone scaffolds by Pictet-Spengler spirocyclisation using β-cyclodextrin-SO3H as a recyclable catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2019.02.062openalex-snapshot
PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130536openalex-snapshot
Singlet oxygen mediated one pot synthesis of N-pyridinylamides via oxidative amidation of aryl alkyl ketones
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.02.023openalex-snapshot
Simple and inexpensive threonine-based organocatalysts as highly active and recoverable catalysts for large-scale asymmetric direct stoichiometric aldol reactions on water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.146openalex-snapshot
‘On water’ synthesis of 2,4-diaryl-2,3-dihydro-1,5-benzothiazepines catalysed by sodium dodecyl sulfate (SDS)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.07.055openalex-snapshot
Rapid four-component reactions in water: synthesis of pyranopyrazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.09.079openalex-snapshot
Synthesis of novel annulated uracils via domino Knoevenagel-hetero-Diels–Alder reaction in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.018openalex-snapshot
PEG350-based di-(2-pyridyl)methylamine as a ligand in the Pd-catalyzed water Suzuki–Miyaura reaction of aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.106openalex-snapshot
Facile reaction of thiols and amines with alkyl 4-hydroxy-2-alkynoates in water under neutral conditions and ultrasound irradiation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.172openalex-snapshot
An aqueous medium synthesis and tautomerism study of 3(5)-amino-1,2,4-triazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.10.082openalex-snapshot
The rhodium-catalysed 1,2-addition of arylboronic acids to aldehydes and ketones with sulfonated S-Phos
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.087openalex-snapshot
Solvent-free multicomponent synthesis of pyranopyrazoles: per-6-amino-β-cyclodextrin as a remarkable catalyst and host
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.02.093openalex-snapshot
Efficient and mild synthesis of functionalized 2,3-dihydrofuran derivatives via domino reaction in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.047openalex-snapshot
An efficient one-pot three-component synthesis of functionalized pyrimido[4,5-b]quinolines and indeno fused pyrido[2,3-d]pyrimidines in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.080openalex-snapshot
Convenient and simple synthesis of 2-aminothiazoles by the reaction of α-halo ketone carbonyls with ammonium thiocyanate in the presence of N-methylimidazole
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.025openalex-snapshot
Simple and efficient protocol for the synthesis of novel dihydro-1H-pyrano[2,3-c]pyrazol-6-ones via a one-pot four-component reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.055openalex-snapshot
An efficient one-pot organocatalytic synthesis of 9-(1H-indol-3-yl)-xanthen-4-(9H)-ones under mild aqueous micellar conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.082openalex-snapshot
Water-based conditions for the microscale parallel synthesis of bicyclic lactams
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.133openalex-snapshot
Flavin-catalyzed aerobic oxidation of sulfides in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.12.095openalex-snapshot
An efficient and regioselective one-pot multi-component synthesis of pyrimido[4,5-d]pyrimidine derivatives in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.04.122openalex-snapshot
A four-component synthesis of dihydropyrano[2,3-c]pyrazoles in a new water-based worm-like micellar medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.125openalex-snapshot
Sodium chloride: a proficient additive for the synthesis of pyridine derivatives in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.064openalex-snapshot
Aqueous bile salt accelerated cascade synthesis of 1,2,3-triazoles from arylboronic acids
inferred← citeshttps://doi.org/10.1016/j.tibtech.2008.03.004openalex-snapshot
New opportunities for biocatalysis: making pharmaceutical processes greener
inferred← citeshttps://doi.org/10.1016/s0065-3160(08)00001-4openalex-snapshot
Kinetic medium effects on organic reactions in aqueous colloidal solutions
inferred← citeshttps://doi.org/10.1021/acs.iecr.6b04875openalex-snapshot
Role of Re and Ru in Re–Ru/C Bimetallic Catalysts for the Aqueous Hydrogenation of Succinic Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01053openalex-snapshot
Metal-Free Synthesis of Benzimidazoles via Oxidative Cyclization of d -Glucose with o-Phenylenediamines in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02076openalex-snapshot
Visible Light-Induced Photocatalyst-Free Diastereoselective Iodosulfonylation of Cyclopropenes in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02327openalex-snapshot
A Serendipitous Synthesis of 11a-Hydroxy-11,11a-dihydrobenzo[e]indeno[2,1-b][1,4]diazepine-10,12-dione Derivatives by Condensation of 2-Aminobenzamides with Ninhydrin in Water
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02510openalex-snapshot
Solvent-Free α-Arylation Reaction of Ketones with (Hetero)aryl Chlorides by N -Heterocyclic Carbene–Palladium Complex (SIPr) Ph2 Pd(cin)Cl
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01850openalex-snapshot
“On Water” C(sp3)–H Functionalization/C–O/C–N Bonds Formations: Synthesis of Functionalized Oxazolidines and Imidazolidines
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01679openalex-snapshot
Concentrated Aqueous Sodium Tosylate as Green Medium for Alkene Oxidation and Nucleophilic Substitution Reactions
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00266openalex-snapshot
“On-Water” Reaction of (Thio)isocyanate: A Sustainable Process for the Synthesis of Unsymmetrical (Thio)ureas
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03395openalex-snapshot
N-Iodosuccinimide-Promoted [3 + 2] Annulation Reaction of Aryldiazonium Salts with Guanidines To Construct Aminotetrazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01663openalex-snapshot
Design and Discovery of Water-Soluble Benzooxaphosphole-Based Ligands for Hindered Suzuki–Miyaura Coupling Reactions with Low Catalyst Load
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00303openalex-snapshot
Additive-Free Decarboxylative Coupling of Cinnamic Acid Derivatives in Water: Synthesis of Allyl Amines
inferred← citeshttps://doi.org/10.1021/acsami.4c04739openalex-snapshot
Elucidating the Synergistic Promotional Mechanism of Water and Oxygen in the Aerobic C–C Homocoupling Reaction Catalyzed by Visible-Light-Derived Core–Shell Pd@A-CQDs Nanostructures
inferred← citeshttps://doi.org/10.1021/acscatal.0c01196openalex-snapshot
Scalable α-Arylation of Nitriles in Aqueous Micelles using Ultrasmall Pd Nanoparticles: Surprising Formation of Carbanions in Water
inferred← citeshttps://doi.org/10.1021/acscatal.2c05288openalex-snapshot
Trichloromethyl Carbanion in Aqueous Micelles: Mechanistic Insights and Access to Carboxylic Acids from (Hetero)aryl Halides
inferred← citeshttps://doi.org/10.1021/acscatal.8b02509openalex-snapshot
Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis
inferred← citeshttps://doi.org/10.1021/acsomega.8b01501openalex-snapshot
TEMPO-Catalyzed Direct Conversion of Primary Alcohols to α-Chloroacetals with TCCA Both as an Oxidant and a Chlorination Reagent
inferred← citeshttps://doi.org/10.1021/acsomega.8b03051openalex-snapshot
Recent Advances in the Nanocatalyst-Assisted NaBH4 Reduction of Nitroaromatics in Water
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c01577openalex-snapshot
Reactivity of Styrenes in Micelles: Safe, Selective, and Sustainable Functionalization with Azides and Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acssuschemeng.4c05293openalex-snapshot
“In-Water” Three-Component One-Pot Reaction for the Facile Synthesis of Densely Functionalized 2,3-Dihydro-1H-pyrrol-2-ols and Mechanistic Insight
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b00045openalex-snapshot
Magnetically Retrievable Rh(0) Nanocomposite as Relevant Catalyst for Mild Hydrogenation of Functionalized Arenes in Water
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b01718openalex-snapshot
Practical Approach for Quantitative Green Esterifications
inferred← citeshttps://doi.org/10.1021/cc100047jopenalex-snapshot
Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones by Three-Component Coupling of Isatoic Anhydride, Amines, and Aldehydes Catalyzed by Magnetic Fe3O4 Nanoparticles in Water
inferred← citeshttps://doi.org/10.1021/cc800212vopenalex-snapshot
Synthesis of Isoxazolo[5,4-b]pyridines by Microwave-Assisted Multi-Component Reactions in Water
inferred← citeshttps://doi.org/10.1021/cg700953kopenalex-snapshot
In situ and Ex situ Analysis of Salmeterol Xinafoate Microcrystal Formation from Poly(ethylene glycol) 400−Water Cosolvent Mixtures
inferred← citeshttps://doi.org/10.1021/cr100209dopenalex-snapshot
Intermolecular Dehydrogenative Heck Reactions
inferred← citeshttps://doi.org/10.1021/ic2009094openalex-snapshot
Novel Heterotetranuclear V2Mo2 or V2W2 Complexes with 4,4′-Di-tert-butyl-2,2′-bipyridine: Syntheses, Crystal Structures, and Catalytic Activities
inferred← citeshttps://doi.org/10.1021/ja078057+openalex-snapshot
Effect of Water on the Catalytic Oxidation of Catechols
inferred← citeshttps://doi.org/10.1021/ja802370copenalex-snapshot
Peptide Synthesis in Aqueous Environments: The Role of Extreme Conditions on Amino Acid Activation
inferred← citeshttps://doi.org/10.1021/ja9032742openalex-snapshot
Peptide Synthesis in Aqueous Environments: The Role of Extreme Conditions on Peptide Bond Formation and Peptide Hydrolysis
inferred← citeshttps://doi.org/10.1021/jacs.6c02938openalex-snapshot
Aqueous-Based Biomimetic Porphyrin-Catalyzed Surface Oxidation of Polyethylenes for Enhanced 3D-Printability
inferred← citeshttps://doi.org/10.1021/jacsau.0c00087openalex-snapshot
Metal–Micelle Cooperativity: Phosphine Ligand-Free Ultrasmall Palladium(II) Nanoparticles for Oxidative Mizoroki–Heck-type Couplings in Water at Room Temperature
inferred← citeshttps://doi.org/10.1021/jacsau.2c00367openalex-snapshot
Catalytically Active Multicompartment Micelles
inferred← citeshttps://doi.org/10.1021/jo800980copenalex-snapshot
C−H Carbene Insertion of α-Diazo Acetamides by Photolysis in Non-Conventional Media
inferred← citeshttps://doi.org/10.1021/ol201877vopenalex-snapshot
An Expeditious and Efficient Synthesis of Highly Functionalized [1,6]-Naphthyridines under Catalyst-Free Conditions in Aqueous Medium
inferred← citeshttps://doi.org/10.1021/ol302034ropenalex-snapshot
Fischer Indole Synthesis in Low Melting Mixtures
inferred← citeshttps://doi.org/10.1021/op4001274openalex-snapshot
Kinetic Analysis of Aqueous-Phase Pd-Catalyzed, Cu-Free Direct Arylation of Terminal Alkynes Using a Hydrophilic Ligand
inferred← citeshttps://doi.org/10.1039/9781782626763-00137openalex-snapshot
Efficient Transformation of Biomass-derived Compounds into Different Valuable Products: A “Green” Approach
inferred← citeshttps://doi.org/10.1039/9781839167461-00035openalex-snapshot
Green Corrosion Inhibition: Concepts of Green Chemistry
inferred← citeshttps://doi.org/10.1039/9781847559524-00044openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1039/9781849736824-00082openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1039/b710414fopenalex-snapshot
“On water” organic synthesis: a highly efficient and clean synthesis of 2-aryl/heteroaryl/styryl benzothiazoles and 2-alkyl/aryl alkyl benzothiazolines
inferred← citeshttps://doi.org/10.1039/b810684copenalex-snapshot
Succinic acid from renewable resources as a C 4 building-block chemical—a review of the catalytic possibilities in aqueous media
inferred← citeshttps://doi.org/10.1039/b900137aopenalex-snapshot
Simple and quick preparation of α-thiocyanate ketones in hydroalcoholic media. Access to 5-aryl-2-imino-1,3-oxathiolanes
inferred← citeshttps://doi.org/10.1039/b900807aopenalex-snapshot
Selective aerobic oxidation of styrene to benzaldehyde catalyzed by water-soluble palladium(II) complex in water
inferred← citeshttps://doi.org/10.1039/b909964fopenalex-snapshot
Recent developments in the utilization of green solvents in polymer chemistry
inferred← citeshttps://doi.org/10.1039/b916765jopenalex-snapshot
Water as the medium of choice for the 1,3-dipolar cycloaddition reactions of hydrophobic nitrones
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