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Surfactant-type asymmetric organocatalyst: organocatalytic asymmetric Michael addition to nitrostyrenes in water
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.200404037openalex-snapshot
The Use of N‐Alkyl‐2,2′‐bipyrrolidine Derivatives as Organocatalysts for the Asymmetric Michael Addition of Ketones and Aldehydes to Nitroolefins
inferredcites →https://doi.org/10.1002/adsc.200505373openalex-snapshot
Small Peptide‐Catalyzed Enantioselective Addition of Ketones to Nitroolefins
inferredcites →https://doi.org/10.1002/ange.200502488openalex-snapshot
Highly Diastereo‐ and Enantioselective Direct Aldol Reactions in Water
inferredcites →https://doi.org/10.1002/anie.200400650openalex-snapshot
In the Golden Age of Organocatalysis
inferredcites →https://doi.org/10.1002/anie.200461959openalex-snapshot
Direct, Highly Enantioselective Pyrrolidine Sulfonamide Catalyzed Michael Addition of Aldehydes to Nitrostyrenes
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.200500599openalex-snapshot
Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes
inferredcites →https://doi.org/10.1002/anie.200502488openalex-snapshot
Highly Diastereo‐ and Enantioselective Direct Aldol Reactions in Water
inferredcites →https://doi.org/10.1002/anie.200600048openalex-snapshot
Functionalized Chiral Ionic Liquids as Highly Efficient Asymmetric Organocatalysts for Michael Addition to Nitroolefins
inferredcites →https://doi.org/10.1002/chem.200600115openalex-snapshot
Enantio‐ and Diastereoselective Michael Addition Reactions of Unmodified Aldehydes and Ketones with Nitroolefins Catalyzed by a Pyrrolidine Sulfonamide
inferredcites →https://doi.org/10.1002/chin.200503030openalex-snapshot
5‐Pyrrolidin‐2‐yltetrazole as an Asymmetric Organocatalyst for the Addition of Ketones to Nitro‐Olefins.
inferredcites →https://doi.org/10.1002/chin.200624079openalex-snapshot
Organocatalytic Direct Asymmetric Aldol Reactions in Water.
inferredcites →https://doi.org/10.1002/hlca.19810640518openalex-snapshot
Synthesis of Open‐Chain 2,3‐Disubstituted 4‐nitroketones by Diastereoselective Michael‐addition of (E)‐Enamines to (E)‐Nitroolefins. A topological rule for C, C‐bond forming processes between prochiral centres. Preliminary communication
inferredcites →https://doi.org/10.1002/hlca.200490125openalex-snapshot
Studies on Direct Stereoselective Aldol Reactions in Aqueous Media
inferredcites →https://doi.org/10.1002/pol.1978.170160507openalex-snapshot
Anionic‐initiated polymerization of β‐nitrostyrenes
inferredcites →https://doi.org/10.1002/recl.19961151103openalex-snapshot
Lewis‐acid catalysis of carbon carbon bond forming reactions in water
inferredcites →https://doi.org/10.1016/j.cplett.2004.10.127openalex-snapshot
Aggregation and micelle formation of ionic liquids in aqueous solution
inferredcites →https://doi.org/10.1016/j.talanta.2004.01.001openalex-snapshot
Behaviour of a binary solvent mixture constituted by an amphiphilic ionic liquid, 1-decyl-3-methylimidazolium bromide and water
inferredcites →https://doi.org/10.1016/j.tetasy.2006.01.034openalex-snapshot
A highly enantioselective organocatalyst for the Michael addition of cyclic ketones to nitroolefins
inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.112openalex-snapshot
Protonated chiral prolinamide catalyzed enantioselective direct aldol reaction in water
inferredcites →https://doi.org/10.1016/s0013-4686(97)85506-5openalex-snapshot
Addition of electrochemically-generated anions to aldehydes and olefins: effect of reaction medium and anion basicity
inferredcites →https://doi.org/10.1016/s0040-4039(02)01500-9openalex-snapshot
Amine-catalyzed direct self Diels–Alder reactions of α,β-unsaturated ketones in water: synthesis of pro-chiral cyclohexanones
inferredcites →https://doi.org/10.1016/s0040-4039(03)00692-0openalex-snapshot
Proline catalyzed aldol reactions in aqueous micelles: an environmentally friendly reaction system
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/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/ja001420ropenalex-snapshot
Organic Synthesis Inside Particles in Water: Lewis Acid−Surfactant-Combined Catalysts for Organic Reactions in Water Using Colloidal Dispersions as Reaction Media
inferredcites →https://doi.org/10.1021/ja010037zopenalex-snapshot
Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon−Carbon Bond-Forming Reactions
inferredcites →https://doi.org/10.1021/ja026241jopenalex-snapshot
Dehydration Reactions in Water. Brønsted Acid−Surfactant-Combined Catalyst for Ester, Ether, Thioether, and Dithioacetal Formation in Water
inferredcites →https://doi.org/10.1021/ja046871gopenalex-snapshot
A New Class of Chiral Pyrrolidine−Pyridine Conjugate Base Catalysts for Use in Asymmetric Michael Addition Reactions
inferredcites →https://doi.org/10.1021/ja0573312openalex-snapshot
Organocatalytic Direct Asymmetric Aldol Reactions in Water
inferredcites →https://doi.org/10.1021/ja060338eopenalex-snapshot
Organocatalytic Direct Michael Reaction of Ketones and Aldehydes with β-Nitrostyrene in Brine
inferredcites →https://doi.org/10.1021/ja0620890openalex-snapshot
Highly Enantioselective Direct Conjugate Addition of Ketones to Nitroalkenes Promoted by A Chiral Primary Amine−Thiourea Catalyst
inferredcites →https://doi.org/10.1021/ja9816537openalex-snapshot
Million-Fold Acceleration of a Diels−Alder Reaction due to Combined Lewis Acid and Micellar Catalysis in Water
inferredcites →https://doi.org/10.1021/ol015611qopenalex-snapshot
Efficient Catalysis of a Diels−Alder Reaction by Metallo-Vesicles in Aqueous Solution
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/ol0607490openalex-snapshot
3,3‘-Bimorpholine Derivatives as a New Class of Organocatalysts for Asymmetric Michael Addition
inferredcites →https://doi.org/10.1039/a802825gopenalex-snapshot
Novel application of chiral micellar media to the Diels–Alder reaction
inferredcites →https://doi.org/10.1039/a904439fopenalex-snapshot
Catalytic asymmetric aldol reactions in water
inferredcites →https://doi.org/10.1039/b205425fopenalex-snapshot
1-n-Butyl-3-methylimidazolium ([bmim]) octylsulfate—an even ‘greener’ ionic liquid
inferredcites →https://doi.org/10.1039/b207664kopenalex-snapshot
Direct organocatalytic aldol reactions in buffered aqueous media
inferredcites →https://doi.org/10.1039/b305672dopenalex-snapshot
Hydrophobic interactions and chemical reactivity
inferredcites →https://doi.org/10.1039/b409646kopenalex-snapshot
5-Pyrrolidin-2-yltetrazole as an asymmetric organocatalyst for the addition of ketones to nitro-olefins
inferredcites →https://doi.org/10.1039/b512542aopenalex-snapshot
Organocatalytic asymmetric epoxidation reactions in water–alcohol solutions
inferredcites →https://doi.org/10.1039/b514783mopenalex-snapshot
Simple highly modular acyclic amine-catalyzed direct enantioselective addition of ketones to nitro-olefins
inferredcites →https://doi.org/10.1039/b515880jopenalex-snapshot
The small peptide-catalyzed direct asymmetric aldol reaction in water
inferredcites →https://doi.org/10.1039/b517937hopenalex-snapshot
Highly enantioselective addition of ketones to nitroolefins catalyzed by new thiourea–amine bifunctional organocatalysts
inferredcites →https://doi.org/10.1039/b606154kopenalex-snapshot
Asymmetric aldol reactions catalyzed by tryptophan in water
inferredcites →https://doi.org/10.1039/ji9598300609openalex-snapshot
Journal of the Royal Institute of Chemistry. November 1959
inferredcites →https://doi.org/10.1055/s-2002-19336openalex-snapshot
Proline-Catalyzed Enantioselective Michael Additions of Ketones to Nitrostyrene
inferredcites →https://doi.org/10.3184/030823403103173318openalex-snapshot
Chiral Anionic Surfactants for Asymmetric Mukaiyama Aldol-Type Reaction in Water
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.4765444openalex-extracted
Cobalt(Ii) Catalyzed Michael-Type Hydroarylamination of Activated Olefins
inferred← citeshttps://doi.org/10.1002/0471264180.or090.01openalex-snapshot
The Catalytic, Enantioselective Michael Reaction
inferred← citeshttps://doi.org/10.1002/9780470584248.ch8openalex-snapshot
Asymmetric CarbonCarbon Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9780470711828.ch10openalex-snapshot
Organic Synthesis in Water
inferred← citeshttps://doi.org/10.1002/9780470711828.ch5openalex-snapshot
Supported Asymmetric Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781118158753.ch10openalex-snapshot
“Nonsolvent” Applications of Ionic Liquids in Organocatalysis
inferred← citeshttps://doi.org/10.1002/9781119288152.ch12openalex-snapshot
Asymmetric Organocatalysis in Aqueous Media
inferred← citeshttps://doi.org/10.1002/9781119757153.ch14openalex-snapshot
Asymmetric Organocatalysis in Alternative Media
inferred← citeshttps://doi.org/10.1002/9783527658862.ch1openalex-snapshot
Proline‐Related Secondary Amine Catalysts and Applications
inferred← citeshttps://doi.org/10.1002/9783527658862.ch22openalex-snapshot
Ionic Liquid Organocatalysts
inferred← citeshttps://doi.org/10.1002/9783527658862.ch24openalex-snapshot
Water in Organocatalytic Reactions
inferred← citeshttps://doi.org/10.1002/9783527675906.ch8openalex-snapshot
Emulsion Catalysis: Interface between Homogeneous and Heterogeneous Catalysis
inferred← citeshttps://doi.org/10.1002/9783527814923.ch14openalex-snapshot
Supramolecular Catalysis in Water
inferred← citeshttps://doi.org/10.1002/adsc.200800145openalex-snapshot
Enantioselective Michael Addition of Dicyanoolefins to α,β‐Unsaturated Aldehydes in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/adsc.200800445openalex-snapshot
A Novel Bifunctional Sulfonamide Primary Amine‐Catalyzed Enantioselective Conjugate Addition of Ketones to Nitroolefins
inferred← citeshttps://doi.org/10.1002/adsc.200800731openalex-snapshot
Water in Stereoselective Organocatalytic Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201000162openalex-snapshot
Sugar‐Based Pyrrolidine as a Highly Enantioselective Organocatalyst for Asymmetric Michael Addition of Ketones to Nitrostyrenes
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.201100395openalex-snapshot
The Application of a Recyclable Organocatalytic System to the Asymmetric Domino Michael/Henry Reaction in Aqueous Media
inferred← citeshttps://doi.org/10.1002/adsc.201200215openalex-snapshot
Asymmetric Michael Reaction of Acetaldehyde with Nitroolefins Catalyzed by Highly Water‐Compatible Organocatalysts 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/ange.200703261openalex-snapshot
Water‐Compatible Iminium Activation: Organocatalytic Michael Reactions of Carbon‐Centered Nucleophiles with Enals
inferred← citeshttps://doi.org/10.1002/ange.200703305openalex-snapshot
“Nonsolvens”‐Anwendungen von ionischen Flüssigkeiten bei Biotransformationen und in der Organokatalyse
inferred← citeshttps://doi.org/10.1002/ange.200703459openalex-snapshot
DNA‐Based Catalytic Enantioselective Michael Reactions in Water
inferred← citeshttps://doi.org/10.1002/ange.200703606openalex-snapshot
Highly Efficient Asymmetric Direct Stoichiometric Aldol Reactions on/in Water
inferred← citeshttps://doi.org/10.1002/ange.200902945openalex-snapshot
Polarity‐Directed One‐Pot Asymmetric Cascade Reactions Mediated by Two Catalysts in an Aqueous Buffer
inferred← citeshttps://doi.org/10.1002/ange.201206438openalex-snapshot
The Synthesis of Chiral Isotetronic Acids with Amphiphilic Imidazole/Pyrrolidine Catalysts Assembled in Oil‐in‐Water Emulsion Droplets
inferred← citeshttps://doi.org/10.1002/ange.201402069openalex-snapshot
Grenzflächenkatalyse in Pickering‐Zweiphasensystemen: vom Emulsionsdesign zu grünen Reaktionen
inferred← citeshttps://doi.org/10.1002/anie.200703261openalex-snapshot
Water‐Compatible Iminium Activation: Organocatalytic Michael Reactions of Carbon‐Centered Nucleophiles with Enals
inferred← citeshttps://doi.org/10.1002/anie.200703305openalex-snapshot
“Nonsolvent” Applications of Ionic Liquids in Biotransformations and Organocatalysis
inferred← citeshttps://doi.org/10.1002/anie.200703459openalex-snapshot
DNA‐Based Catalytic Enantioselective Michael Reactions in Water
inferred← citeshttps://doi.org/10.1002/anie.200703606openalex-snapshot
Highly Efficient Asymmetric Direct Stoichiometric Aldol Reactions on/in Water
inferred← citeshttps://doi.org/10.1002/anie.200902945openalex-snapshot
Polarity‐Directed One‐Pot Asymmetric Cascade Reactions Mediated by Two Catalysts in an Aqueous Buffer
inferred← citeshttps://doi.org/10.1002/anie.201206438openalex-snapshot
The Synthesis of Chiral Isotetronic Acids with Amphiphilic Imidazole/Pyrrolidine Catalysts Assembled in Oil‐in‐Water Emulsion Droplets
inferred← citeshttps://doi.org/10.1002/anie.201402069openalex-snapshot
Pickering Interfacial Catalysis for Biphasic Systems: From Emulsion Design to Green Reactions
inferred← citeshttps://doi.org/10.1002/asia.200700417openalex-snapshot
α,α‐Diarylprolinol Ethers: New Tools for Functionalization of Carbonyl Compounds
inferred← citeshttps://doi.org/10.1002/asia.200900080openalex-snapshot
Functionalized Chiral Ionic Liquids: A New Type of Asymmetric Organocatalysts and Nonclassical Chiral Ligands
inferred← citeshttps://doi.org/10.1002/cctc.201300097openalex-snapshot
Optimizing the Structure of 4‐Dialkylamino‐α,α‐diarylprolinol Ethers as Catalysts for the Enantioselective Cyclopropanation of α,β‐Unsaturated Aldehydes in Water
inferred← citeshttps://doi.org/10.1002/chem.200701129openalex-snapshot
Noncovalently Supported Heterogeneous Chiral Amine Catalysts for Asymmetric Direct Aldol and Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/chem.200902509openalex-snapshot
Asymmetric SN1 α‐Alkylation of Cyclic Ketones Catalyzed by Functionalized Chiral Ionic Liquid (FCIL) Organocatalysts
inferred← citeshttps://doi.org/10.1002/chem.201101730openalex-snapshot
Polystyrene‐Supported Diarylprolinol Ethers as Highly Efficient Organocatalysts for Michael‐Type Reactions
inferred← citeshttps://doi.org/10.1002/chem.201102474openalex-snapshot
Polymer‐Supported Enantioselective Bifunctional Catalysts for Nitro‐Michael Addition of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/chem.202501446openalex-snapshot
The Ascent of Supramolecular Polymers and Gels in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1002/chin.200704095openalex-snapshot
Surfactant‐Type Asymmetric Organocatalyst: Organocatalytic Asymmetric Michael Addition to Nitrostyrenes in Water.
inferred← citeshttps://doi.org/10.1002/ejoc.200700031openalex-snapshot
Asymmetric Conjugate Addition of Ketones to β‐Nitrostyrenes by Means of 1,2‐Amino‐Alcohol‐Derived Prolinamides as Bifunctional Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.200700856openalex-snapshot
2‐[(Imidazolylthio)methyl]pyrrolidine as a Trifunctional Organocatalyst for the Highly Asymmetric Michael Addition of Ketones to Nitroolefins
inferred← citeshttps://doi.org/10.1002/ejoc.200701122openalex-snapshot
Organocatalytic Double Michael Reaction of 7‐Oxohept‐2‐enoates and Nitrostyrene – Formal Synthesis of (–)‐α‐ and (–)‐β‐Lycorane
inferred← citeshttps://doi.org/10.1002/ejoc.200800915openalex-snapshot
Chiral Amine–Polyoxometalate Hybrids as Recoverable Asymmetric Enamine Catalysts under Neat and Aqueous Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.200900716openalex-snapshot
Simple Chiral Pyrrolidine–Pyridine‐Based Catalysts for Highly Enantioselective Michael Addition to Nitro Olefins
inferred← citeshttps://doi.org/10.1002/ejoc.201000569openalex-snapshot
C3‐Symmetric Proline‐Functionalized Organocatalysts: Enantioselective Michael Addition Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.201000609openalex-snapshot
Functionalized Chiral Ionic Liquid Catalyzed Asymmetric S N 1 α‐Alkylation of Ketones and Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201000945openalex-snapshot
Highly Enantioselective Michael Addition of Acetone to Nitro Olefins Catalyzed by Chiral Bifunctional Primary Amine‐Thiophosphoramide Catalyst
inferred← citeshttps://doi.org/10.1002/ejoc.201001211openalex-snapshot
4‐Aminothioureaprolinal Dithioacetal as a Catalyst for Highly Enantioselective Michael Additions of Ketones and Aldehydes to Nitroolefins
inferred← citeshttps://doi.org/10.1002/ejoc.201101086openalex-snapshot
Highly Enantioselective Michael Additions of Isobutyraldehyde to Nitroalkenes Promoted by Amphiphilic Bifunctional Primary Amine‐Thioureas in Organic or Aqueous Medium
inferred← citeshttps://doi.org/10.1002/ejoc.201300431openalex-snapshot
An Eco‐Friendly Asymmetric Organocatalytic Conjugate Addition of Malonates to α,β‐Unsaturated Aldehydes: Application on the Synthesis of Chiral Indoles
inferred← citeshttps://doi.org/10.1002/ejoc.201500913openalex-snapshot
Unmodified Primary Amine Organocatalysts for Asymmetric Michael Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/ejoc.202000648openalex-snapshot
A pH‐Switchable Aqueous Organocatalysis with Amphiphilic Secondary Amine–Porphyrin Hybrids
inferred← citeshttps://doi.org/10.1002/ejoc.202401466openalex-snapshot
Efficient Synthesis of Indolyl Benzo[b]Carbazoles via Surfactant‐Type Brønsted Acid‐Catalyzed Three‐Component Cyclization of Ortho‐Formylarylketones with Indoles
inferred← citeshttps://doi.org/10.1002/jsde.12270openalex-snapshot
Aggregation Behavior of Imidazolium‐Based Amino Acid Ionic Liquid Surfactants in Aqueous Solution: The Effect of Amino Acid Counterions
inferred← citeshttps://doi.org/10.1002/macp.201500522openalex-snapshot
Helical Polymers Showing Inverse Helicity and Synergistic Effect in Chiral Catalysis: Catalytic Functionality Determining Enantioconfiguration and Helical Frameworks Providing Asymmetric Microenvironment
inferred← citeshttps://doi.org/10.1002/tcr.201700020openalex-snapshot
Journey Heading towards Enantioselective Synthesis Assisted by Organocatalysis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1579-9_8openalex-snapshot
Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles
inferred← citeshttps://doi.org/10.1007/s10562-010-0351-yopenalex-snapshot
Acyclic Amino Acids Catalyzed Direct Asymmetric Aldol Reactions in Aqueous Media Assisted by 2,4-Dinitrophenol
inferred← citeshttps://doi.org/10.1007/s10562-011-0649-4openalex-snapshot
Pyrrolidine-Based Chiral Quaternary Alkylammonium Ionic Liquids as Organocatalysts for Asymmetric Michael Additions
inferred← citeshttps://doi.org/10.1007/s11164-011-0480-yopenalex-snapshot
Chiral pyrrolidine quaternary derivatives as organocatalysts for asymmetric Michael additions
inferred← citeshttps://doi.org/10.1007/s11164-012-0667-xopenalex-snapshot
A new chiral primary–tertiary diamine-Brønsted acid salt organocatalyst for the highly enantioselective direct anti-aldol and syn-Mannich reactions
inferred← citeshttps://doi.org/10.1007/s11224-014-0409-3openalex-snapshot
Theoretical investigation on mechanism of asymmetric Michael addition of trans-1-nitro-2-phenylethylene to 2-methylpropionaldehyde catalyzed by a Cinchona alkaloid-derived primary amine
inferred← citeshttps://doi.org/10.1007/s11434-010-3120-9openalex-snapshot
Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes
inferred← citeshttps://doi.org/10.1007/s12039-017-1371-6openalex-snapshot
Enantioselective aminocatalysis: Michael addition of unactivated ketones to nitroolefins catalyzed by D-fructose derived monofunctional primary amine
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00405-5openalex-snapshot
4.03 Organocatalytic Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-819542-0.00006-3openalex-snapshot
Stereoselective organic synthesis in water: Organocatalysis by proline and its derivatives
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.08.014openalex-snapshot
d-Glucosamine, a natural aminosugar as organocatalyst for an ecofriendly direct aldol reaction of ketones with aromatic aldehydes in water
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.12.006openalex-snapshot
Catalytic asymmetric formation of carbon–carbon bond in the presence of water
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2024.134202openalex-snapshot
Chiral Janus emulsions with gold nanocomposite for enantioselective catalysis
inferred← citeshttps://doi.org/10.1016/j.jcat.2012.11.024openalex-snapshot
An effective heterogeneous l-proline catalyst for the direct asymmetric aldol reaction using graphene oxide as support
inferred← citeshttps://doi.org/10.1016/j.jcat.2015.12.012openalex-snapshot
Thermo-responsive self-assembled metallomicelles accelerate asymmetric sulfoxidation in water
inferred← citeshttps://doi.org/10.1016/j.mencom.2010.03.001openalex-snapshot
Ionic liquids as substrate-specific recoverable solvents and catalysts of regio-, stereo- and enantioselective organic reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.079openalex-snapshot
Functionalized ionic liquids catalyzed direct aldol reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.08.096openalex-snapshot
Facile evolution of asymmetric organocatalysts in water assisted by surfactant Brønsted acids
inferred← citeshttps://doi.org/10.1016/j.tet.2008.09.085openalex-snapshot
Surfactant-type catalysts in organic reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.09.005openalex-snapshot
Highly enantioselective desymmetrization of meso- and prochiral cyclic ketones via organocatalytic Michael reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2009.11.015openalex-snapshot
Nano-organocatalyst: magnetically retrievable ferrite-anchored glutathione for microwave-assisted Paal–Knorr reaction, aza-Michael addition, and pyrazole synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2010.05.054openalex-snapshot
An effective aza-Michael addition of aromatic amines to electron-deficient alkenes in alkaline Al2O3
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.082openalex-snapshot
Green, efficient and practical Michael addition of arylamines to α,β-unsaturated ketones
inferred← citeshttps://doi.org/10.1016/j.tet.2012.09.071openalex-snapshot
Novel aminoimidazole derived proline organocatalysts for aldol reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.133openalex-snapshot
Enantioselective Michael addition reactions in water using a DNA-based catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2016.11.052openalex-snapshot
Highly enantioselective aldol reactions catalyzed by reusable upper rim-functionalized calix[4]arene-based l -proline organocatalyst in aqueous conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2017.10.008openalex-snapshot
Prolinal dithioacetals: Highly efficient organocatalysts for the direct nitro-Michael additions in both organic and aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.12.003openalex-snapshot
Combining proline and ‘click chemistry’: a class of versatile organocatalysts for the highly diastereo- and enantioselective Michael addition in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.01.023openalex-snapshot
Organocatalytic asymmetric conjugate additions
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.07.021openalex-snapshot
Pyrrolidine–pyridinium based organocatalysts for highly enantioselective Michael addition of cyclohexanone to nitroalkenes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.10.016openalex-snapshot
Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent
inferred← citeshttps://doi.org/10.1016/j.tetasy.2008.12.007openalex-snapshot
New pyrrolidine-triazole-based C2 symmetric organocatalysts and their utility in the asymmetric Michael reaction of β-nitrostyrenes and the synthesis of nitrochromenes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.02.036openalex-snapshot
Asymmetric transfer hydrogenation in aqueous media catalyzed by resin-supported peptide having a polyleucine tether
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.05.032openalex-snapshot
Highly efficient primary amine organocatalysts for the direct asymmetric aldol reaction in brine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.09.019openalex-snapshot
Highly diastereo- and enantioselective direct aldol reactions by 4-tert-butyldimethylsiloxy-substituted organocatalysts derived from N-prolylsulfonamides in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.08.012openalex-snapshot
Hydroxyphthalimide allied triazole-pyrrolidine catalyst for asymmetric Michael additions in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.10.009openalex-snapshot
Chiral quaternary alkylammonium ionic liquid [Pro-dabco][BF4]: as a recyclable and highly efficient organocatalyst for asymmetric Michael addition reactions
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.11.001openalex-snapshot
Asymmetric organocatalytic synthesis of γ-nitrocarbonyl compounds through Michael and Domino reactions
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.04.010openalex-snapshot
A chiral pyrrolidine-pyrazole catalyst for the enantioselective Michael addition of carbonyls to nitroolefins
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.11.009openalex-snapshot
Catalytic asymmetric carbon–carbon bond-forming reactions in aqueous media
inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.11.023openalex-snapshot
Asymmetric triple cascade organocatalytic reaction in water: construction of polyfunctional cyclohexene building blocks having multiple stereocenters
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.06.026openalex-snapshot
Chiral amine catalyzed enantio- and diastereoselective Michael reaction in brine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2013.11.002openalex-snapshot
Direct asymmetric Michael addition of ketones to chalcones catalyzed by a hydroxyphthalimide derived triazole–pyrrolidine
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.02.003openalex-snapshot
Sugar amide-pyrrolidine catalyst for the asymmetric Michael addition of ketones to nitroolefins
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.06.009openalex-snapshot
Enantioselective Michael addition of α,α-disubstituted aldehydes to nitroolefins catalyzed by a pyrrolidine-pyrazole
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.07.005openalex-snapshot
Asymmetric Michael addition of aldehydes to nitroolefins catalyzed by a pyrrolidine–pyrazole
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.10.014openalex-snapshot
Pyrrolidine-oxyimides: new chiral catalysts for enantioselective Michael addition of ketones to nitroolefins in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.08.006openalex-snapshot
Pyrrolidine-HOBt: an oxytriazole catalyst for the enantioselective Michael addition of cyclohexanone to nitroolefins in water
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.02.005openalex-snapshot
Enantioselective Michael addition of aldehydes to nitroolefins catalyzed by pyrrolidine-HOBt
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.085openalex-snapshot
Synthesis of prolinal dithioacetals as catalysts for the highly stereoselective Michael addition of ketones and aldehydes to β-nitrostyrenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.09.168openalex-snapshot
An enantioselective Michael addition of malonate to nitroalkenes catalyzed by low loading demethylquinine salts in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.10.008openalex-snapshot
Tandem bis-aza-Michael addition reaction of amines in aqueous medium promoted by polystyrenesulfonic acid
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.12.024openalex-snapshot
Pyrrolidine-based chiral pyridinium ionic liquids (ILs) as recyclable and highly efficient organocatalysts for the asymmetric Michael addition reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.03.131openalex-snapshot
Organo-catalyzed highly diastereo- and enantio-selective direct aldol reactions in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.120openalex-snapshot
Rationally designed 4-phenoxy substituted prolinamide phenols organocatalyst for the direct aldol reaction in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.211openalex-snapshot
4-Trifluoromethanesulfonamidyl prolinol tert-butyldiphenylsilyl ether as a highly efficient bifunctional organocatalyst for Michael addition of ketones and aldehydes to nitroolefins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.011openalex-snapshot
Highly enantioselective Michael addition reactions in water catalyzed by an insoluble MPS-supported 4-sulfonamidyl prolinol tert-butyldiphenylsilyl ether
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.06.037openalex-snapshot
Organocatalytic asymmetric syn-selective direct aldol reactions in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.07.164openalex-snapshot
Functionalized proline with double hydrogen bonding potential: highly enantioselective Michael addition of carbonyl compounds to β-nitrostyrenes in brine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.08.123openalex-snapshot
Synthesis and application of proline based organocatalyst for highly enantioselective aldol reaction by hydrogen bonding
inferred← citeshttps://doi.org/10.1016/s1872-2067(14)60080-2openalex-snapshot
An amphiphilic organic catalyst for the direct asymmetric Michael addition of cycloketone to nitroolefins in water
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00417openalex-snapshot
Catalytic Organic Reactions in Water toward Sustainable Society
inferred← citeshttps://doi.org/10.1021/acscatal.7b02118openalex-snapshot
Chiral Catalysis at the Water/Oil Interface
inferred← citeshttps://doi.org/10.1021/jo061657ropenalex-snapshot
Evolution of Pyrrolidine-Type Asymmetric Organocatalysts by “Click” Chemistry
inferred← citeshttps://doi.org/10.1021/jo071004qopenalex-snapshot
Insights on Co-Catalyst-Promoted Enamine Formation between Dimethylamine and Propanal through Ab Initio and Density Functional Theory Study
inferred← citeshttps://doi.org/10.1021/jo101188mopenalex-snapshot
Water-Compatible Iminium Activation: Highly Enantioselective Organocatalytic Michael Addition of Malonates to α,β-Unsaturated Enones
inferred← citeshttps://doi.org/10.1021/jo2002819openalex-snapshot
A Recyclable Organocatalyst for Asymmetric Michael Addition of Acetone to Nitroolefins
inferred← citeshttps://doi.org/10.1021/ol0628006openalex-snapshot
Readily Accessible 9-epi-amino Cinchona Alkaloid Derivatives Promote Efficient, Highly Enantioselective Additions of Aldehydes and Ketones to Nitroolefins
inferred← citeshttps://doi.org/10.1021/ol070002popenalex-snapshot
Enantioselective Direct Aldol Reaction “on Water” Promoted by Chiral Organic Catalysts
inferred← citeshttps://doi.org/10.1021/ol100415hopenalex-snapshot
Efficient Asymmetric α-Oxyamination of Aldehydes by Resin-Supported Peptide Catalyst in Aqueous Media
inferred← citeshttps://doi.org/10.1021/ol800031popenalex-snapshot
Organocatalytic Asymmetric Transfer Hydrogenation in Aqueous Media Using Resin-Supported Peptide Having a Polyleucine Tether
inferred← citeshttps://doi.org/10.1021/ol8005369openalex-snapshot
Organocatalytic Enantioselective Domino Michael-aldol Condensation of 5-Oxoalkanal and α,β-Unsaturated Aldehydes. Efficient Assembly of Densely Functionalized Cyclohexenes
inferred← citeshttps://doi.org/10.1021/ol901204bopenalex-snapshot
Di(methylimidazole)prolinol Silyl Ether Catalyzed Highly Michael Addition of Aldehydes to Nitroolefins in Water
inferred← citeshttps://doi.org/10.1039/9781847559760-00001openalex-snapshot
Catalysis in Non-conventional Reaction Media
inferred← citeshttps://doi.org/10.1039/9781849732185-00018openalex-snapshot
Enantioselective Conjugate Addition Reactions via Enamine Activation
inferred← citeshttps://doi.org/10.1039/b611366dopenalex-snapshot
A simple asymmetric organocatalytic approach to optically active cyclohexenones
inferred← citeshttps://doi.org/10.1039/b701216kopenalex-snapshot
Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation
inferred← citeshttps://doi.org/10.1039/b708525gopenalex-snapshot
Organocatalysts wrapped around by poly(ethylene glycol)s (PEGs): a unique host–guest system for asymmetric Michael addition reactions
inferred← citeshttps://doi.org/10.1039/b713843aopenalex-snapshot
Combinatorial synthesis of functionalized chiral and doubly chiral ionic liquids and their applications as asymmetric covalent/non-covalent bifunctional organocatalysts
inferred← citeshttps://doi.org/10.1039/b803209bopenalex-snapshot
Transfer hydrogenation of aldehydes on amphiphilic catalyst assembled at the interface of emulsion droplets
inferred← citeshttps://doi.org/10.1039/b910249copenalex-snapshot
Enantioselective nitro-Michael reactions catalyzed by short peptides on water
inferred← citeshttps://doi.org/10.1039/b916583eopenalex-snapshot
Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water
inferred← citeshttps://doi.org/10.1039/b921538gopenalex-snapshot
CO2-controlled reactors: epoxidation in emulsions with droplet size from micron to nanometre scale
inferred← citeshttps://doi.org/10.1039/b9nj00764dopenalex-snapshot
Supramolecular gels as active media for organic reactions and catalysis
inferred← citeshttps://doi.org/10.1039/c004970kopenalex-snapshot
In water, on water, and by water: mimicking nature's aldolases with organocatalysis and water
inferred← citeshttps://doi.org/10.1039/c0ob00834fopenalex-snapshot
Enantioselective organocatalytic domino Michael–acetalization–Henry reactions of 2-hydroxynitrostyrene and aldehyde for the synthesis of tetrahydro-6H-benzo[c]chromenones
inferred← citeshttps://doi.org/10.1039/c1cs15222jopenalex-snapshot
Green chemistry oriented organic synthesis in water
inferred← citeshttps://doi.org/10.1039/c1cy00318fopenalex-snapshot
Highly efficient direct large-scale stoichiometric aldol reactions catalyzed by a new diamine salt in the presence of water
inferred← citeshttps://doi.org/10.1039/c2ob26248gopenalex-snapshot
Highly enantioselective and recyclable organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in aqueous media
inferred← citeshttps://doi.org/10.1039/c3cs60037hopenalex-snapshot
Supramolecular catalysis. Part 2: artificial enzyme mimics
inferred← citeshttps://doi.org/10.1039/c3ob27398aopenalex-snapshot
Asymmetric Michael reactions catalyzed by a highly efficient and recyclable quaternary ammonium ionic liquid-supported organocatalyst in aqueous media
inferred← citeshttps://doi.org/10.1039/c4cc01759eopenalex-snapshot
Peptide catalysis in aqueous emulsions
inferred← citeshttps://doi.org/10.1039/c5cy00953gopenalex-snapshot
Asymmetric epoxidation of unfunctionalized olefins accelerated by thermoresponsive self-assemblies in aqueous systems
inferred← citeshttps://doi.org/10.1039/c6ob01558aopenalex-snapshot
Binaphthyl-based chiral bifunctional organocatalysts for water mediated asymmetric List–Lerner–Barbas aldol reactions
inferred← citeshttps://doi.org/10.1039/c6ra01130fopenalex-snapshot
Cooperative chiral salen Ti IV catalysts with built-in phase-transfer capability accelerate asymmetric sulfoxidation in water
inferred← citeshttps://doi.org/10.1039/c6ra14399gopenalex-snapshot
Design for carbon–carbon bond forming reactions under ambient conditions
inferred← citeshttps://doi.org/10.1039/c9py00326fopenalex-snapshot
Pyrrolidine-based chiral porous polymers for heterogeneous organocatalysis in water
inferred← citeshttps://doi.org/10.1039/d0cc04410eopenalex-snapshot
A novel chiral surfactant-type metallomicellar catalyst for asymmetric Michael addition in water
inferred← citeshttps://doi.org/10.1055/a-2464-6964openalex-snapshot
Facile Synthesis of 2- and 3-Substituted Indoles Using a Catalytic Amount of Pd/C and 1-Octene System
inferred← citeshttps://doi.org/10.1071/ch12428openalex-snapshot
Water-Assisted Organocatalysis: An Enantioselective Green Protocol for the Henry Reaction
inferred← citeshttps://doi.org/10.1246/cl.2010.412openalex-snapshot
Efficient and Highly Enantioselective Michael Addition of Aldehydes to Nitroalkenes Catalyzed by a Surfactant-type Organocatalyst in the Presence of Water
inferred← citeshttps://doi.org/10.2174/1385272821666170818160915openalex-snapshot
Recent Developments in Enantioselective Organocatalytic Michael Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.2174/1385272824999200801022221openalex-snapshot
Ionic Liquid Assisted C-C Bond Formation
inferred← citeshttps://doi.org/10.3390/catal3030709openalex-snapshot
Ionic Liquid Immobilized Organocatalysts for Asymmetric Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.3390/molecules25153420openalex-snapshot
Chiral Amphiphilic Secondary Amine-Porphyrin Hybrids for Aqueous Organocatalysis
inferred← citeshttps://doi.org/10.3987/com-09-s(s)71openalex-snapshot
Design of Reaction Media for Nucleophilic Substitution Reactions by Using a Catalytic Amount of an Amphiphilic Imidazolium Salt in Water
inferred← citeshttps://doi.org/10.3987/rev-07-621openalex-snapshot
Organocatalytic Asymmetric Synthesis Using Proline and Related Molecules. Part 2.
inferred← citeshttps://doi.org/10.70675/587aa913z42f0z4178z91efz7428077cb4caopenalex-snapshot
Highly efficient enantioselective catalysis through supramolecular chirality amplification
inferred← citeshttps://doi.org/10.7868/s0514749218080101openalex-snapshot
СИНТЕЗ ПРОИЗВОДНЫХ 5H-ХРОМЕНО[2,3-6]ПИРИДИНА С ИСПОЛЬЗОВАНИЕМ УЛЬТРАЗВУКА, "Журнал органической химии"
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.