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DABCO-Based Ionic Liquids: Recyclable Catalysts for Aza-Michael Addition of α,β-Unsaturated Amides under Solvent-Free Conditions

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What this work says

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

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Ionic Liquids Made with Dimethyl Carbonate: Solvents as well as Boosted Basic Catalysts for the Michael Reaction

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Nano‐Fe3O4 Encapsulated‐Silica Particles Bearing 3‐Aminopropyl Group as a Magnetically Separable Catalyst for Efficient Knoevenagel Condensation of Aromatic Aldehydes with Active Methylene Compounds

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Are Ionic Liquids Suitable Media for Organocatalytic Reactions?

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2‐Pyrrolidinecarboxylic Acid Ionic Liquid as a Highly Efficient Organocatalyst for the Asymmetric One‐Pot Mannich Reaction

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A simple, efficient, and green protocol for Knoevenagel condensation in a cost-effective ionic liquid 2-hydroxyethlammonium formate without a catalyst

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Conjugate Addition Reactions in Organic Synthesis

inferredcites →https://doi.org/10.1016/j.aca.2007.12.011openalex-snapshot

Applications of ionic liquids in electrochemical sensors

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Ionic liquids and catalysis: Recent progress from knowledge to applications

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Recyclable copper catalysts based on ionic-tagged C2-symmetric Indabox ligands and their application in asymmetric Henry reactions

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Application of ionic liquids in electrochemical sensing systems

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Ionic liquids in separation techniques

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Electrosynthesis of poly(o-phenylenediamine) in a room temperature ionic liquid

inferredcites →https://doi.org/10.1016/j.jorganchem.2005.03.007openalex-snapshot

Metal-containing ionic liquids and ionic liquid crystals based on imidazolium moiety

inferredcites →https://doi.org/10.1016/j.mencom.2011.01.009openalex-snapshot

Henry and Mannich reactions of polynitroalkanes in ionic liquids

inferredcites →https://doi.org/10.1016/j.molcata.2005.09.012openalex-snapshot

Mannich reaction in Brönsted acidic ionic liquid: A facile synthesis of β-amino carbonyl compounds

inferredcites →https://doi.org/10.1016/j.molcatb.2010.11.011openalex-snapshot

The lipase-catalyzed asymmetric C–C Michael addition

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Investigations on enzyme catalytic promiscuity: The first attempts at a hydrolytic enzyme-promoted conjugate addition of nucleophiles to α,β-unsaturated sulfinyl acceptors

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Stereoselective synthesis of spiro[5.5]undecane derivatives via biocatalytic [5+1] double Michael additions

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Michael additions of dihydropyrimidines and 2-amino-1,3,4-thiadiazoles to α,β-ethylenic compounds: using polyethylene glycols as a green reaction media

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A facile generation of C–S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions

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Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of β-alkoxyketones by the oxa-Michael addition reactions

inferredcites →https://doi.org/10.1016/j.tet.2010.11.018openalex-snapshot

Beyond the chiral pool: a general approach to β-amino-α-keto amides

inferredcites →https://doi.org/10.1016/j.tetlet.2005.03.112openalex-snapshot

Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds

inferredcites →https://doi.org/10.1016/j.tetlet.2006.01.124openalex-snapshot

β-Cyclodextrin promoted aza-Michael addition of amines to conjugated alkenes in water

inferredcites →https://doi.org/10.1016/j.tetlet.2008.03.108openalex-snapshot

Imidazolium-based polymer supported gadolinium triflate as a heterogeneous recyclable Lewis acid catalyst for Michael additions

inferredcites →https://doi.org/10.1016/j.tetlet.2008.09.116openalex-snapshot

Eco-friendly polyethylene glycol promoted Michael addition reactions of α,β-unsaturated carbonyl compounds

inferredcites →https://doi.org/10.1016/j.tetlet.2009.01.123openalex-snapshot

Aza-Michael addition of aliphatic or aromatic amines to α,β-unsaturated compounds catalyzed by a DBU-derived ionic liquid under solvent-free conditions

inferredcites →https://doi.org/10.1016/j.tetlet.2011.11.022openalex-snapshot

Friedel–Crafts acylation using bismuth triflate in [BMI][PF6]

inferredcites →https://doi.org/10.1016/j.tetlet.2013.01.071openalex-snapshot

Simple cleavage of diorganyl diselenides with NaBH4/PEG-400 and direct Michael addition to electron-deficient alkenes

inferredcites →https://doi.org/10.1016/j.tetlet.2014.01.112openalex-snapshot

Michael addition of indoles to β-nitrostyrenes catalyzed by HY zeolite under solvent-free conditions

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Dynamically coating the capillary with 1-alkyl-3-methylimidazolium-based ionic liquids for separation of basic proteins by capillary electrophoresis

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Enantioselective and practical syntheses of R- and S-fluoxetines

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Direct Extraction of Double-Stranded DNA Into Ionic Liquid 1-Butyl-3-methylimidazolium Hexafluorophosphate and Its Quantification

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2-Nitroglycals as Powerful Glycosyl Donors: Application in the Synthesis of Biologically Important Molecules

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Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2

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Room-Temperature Ionic Liquids. Solvents for Synthesis and Catalysis

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Novel Multiple-Acidic Ionic Liquids: Catalysts for Environmentally Friendly Benign Synthesis of trans-β-Nitrostyrenes under Solvent-Free Conditions

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Trisubstituted 2-Trifluoromethyl Pyrrolidines via Catalytic Asymmetric Michael Addition/Reductive Cyclization

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Polyethylene glycol as a non-ionic liquid solvent for Michael addition reaction of amines to conjugated alkenes

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MhyADH catalysed Michael addition of water and in situ oxidation

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Design of Ionic Liquids for Electrochemical Applications

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What points at this work

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

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ChemInform Abstract: DABCO‐Based Ionic Liquids: Recyclable Catalysts for Aza‐Michael Addition of α,β‐Unsaturated Amides under Solvent‐Free Conditions.

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Direct synthesis of carbamate from CO 2 using a task-specific ionic liquid catalyst

inferred← citeshttps://doi.org/10.1039/c7nj03450dopenalex-snapshot

Heterogenization of amine-functionalized ionic liquids using graphene oxide as a support material: a highly efficient catalyst for the synthesis of 3-substituted indoles via Yonemitsu-type reaction

inferred← citeshttps://doi.org/10.1039/c8nj01455hopenalex-snapshot

DABCO-based ionic liquids: introduction of two metal-free catalysts for one-pot synthesis of 1,2,4-triazolo[4,3- a ]pyrimidines and pyrido[2,3- d ]pyrimidines

inferred← citeshttps://doi.org/10.1039/c8nj06054aopenalex-snapshot

Difunctional ammonium ionic liquids with bicyclic cations

inferred← citeshttps://doi.org/10.1039/d0mh01088jopenalex-snapshot

Magnetically supported ionic liquids: a sustainable catalytic route for organic transformations

inferred← citeshttps://doi.org/10.1039/d0py00125bopenalex-snapshot

Organocatalyzed ring-opening polymerization (ROP) of functional β-lactones: new insights into the ROP mechanism and poly(hydroxyalkanoate)s (PHAs) macromolecular structure

inferred← citeshttps://doi.org/10.1039/d3ob00921aopenalex-snapshot

The versatility of DABCO as a reagent in organic synthesis: a review

inferred← citeshttps://doi.org/10.1039/d3ob02006aopenalex-snapshot

Reinvigorating aza-Michael reactions under ionic liquid catalysis: a greener approach

inferred← citeshttps://doi.org/10.1039/d5mr00068hopenalex-snapshot

Mechanochemistry-driven solvent-free synthesis of biologically relevant diversely substituted 2-amino-1,4-naphthoquinones

inferred← citeshttps://doi.org/10.1080/00397911.2018.1546401openalex-snapshot

Efficient protocol for Aza-Michael addition of N-heterocycles to α,β-unsaturated compound using [Ch]OH and [n-butyl urotropinium]OH as basic ionic liquids in aqueous/solvent free conditions

inferred← citeshttps://doi.org/10.1080/00397911.2019.1570268openalex-snapshot

Synthesis of a novel tetracationic acidic organic salt based on DABCO and its applications as catalyst in the Knoevenagel condensation reactions in water

inferred← citeshttps://doi.org/10.1080/10406638.2022.2030765openalex-snapshot

A Dicationic Molten Salt Catalyzed Synthesis of 1,2,4-Triazolopyrimidine, Quinazolinone and Biscoumarin Derivatives under Green Conditions

inferred← citeshttps://doi.org/10.1080/10426507.2017.1417298openalex-snapshot

TiCl2(OTf)-SiO2: A solid stable lewis acid catalyst for Michael addition of α-Aminophosphonates, Amines, Indoles and Pyrrole

inferred← citeshttps://doi.org/10.1080/17518253.2017.1293177openalex-snapshot

Green synthesis of new acyl hydrazide derivatives by single and double aza-Michael reaction under solvent-free conditions

inferred← citeshttps://doi.org/10.1098/rsos.190997openalex-snapshot

New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones

inferred← citeshttps://doi.org/10.1177/1747519819880693openalex-snapshot

Chemoselective aza-Michael addition of indoles to 2-aroyl-1,3-diarylenones

inferred← citeshttps://doi.org/10.1515/hc-2016-0182openalex-snapshot

Regioselective 1,4-conjugate aza-Michael addition of dienones with benzotriazole

inferred← citeshttps://doi.org/10.1515/hc-2022-0009openalex-snapshot

Two independent and consecutive Michael addition of 1,3-dimethylbarbituric acid to (2,6-diarylidene)cyclohexanone: Flying-bird-shaped 2D-polymeric structure

inferred← citeshttps://doi.org/10.2139/ssrn.4866576openalex-snapshot

Development of Cellulose-Supported Pd-Nanocatalyst for the Heck Coupling and Michael Addition Reactions

inferred← citeshttps://doi.org/10.2174/0115701786359672241226141225openalex-snapshot

DABCO-Based Ionic Liquids: A Non-Conventional Catalyst for the Synthesis of N-Substituted 2-Nitrophenylamines

inferred← citeshttps://doi.org/10.2174/2213337207999200831105105openalex-snapshot

Ionic Liquid Catalyzed Efficient Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles Under Metal and Solvent Free Conditions

inferred← citeshttps://doi.org/10.2174/2213346107666191227101538openalex-snapshot

DABCO as a Base and an Organocatalyst in Organic Synthesis: A Review

inferred← citeshttps://doi.org/10.3390/catal7070219openalex-snapshot

Recyclable Fe3O4 Nanoparticles Catalysts for Aza-Michael Addition of Acryl Amides by Magnetic Field

inferred← citeshttps://doi.org/10.3390/molecules24234224openalex-snapshot

Michael Addition Reaction Catalyzed by Imidazolium Chloride to Protect Amino Groups and Construct Medium Ring Heterocycles

inferred← citeshttps://doi.org/10.3390/molecules30132674openalex-snapshot

Catalytic Innovations in the Aza-Michael Reaction: An Experimental Benchmarking Focused on Sustainable Approaches

inferred← citeshttps://doi.org/10.3390/molecules31040628openalex-snapshot

Ionic Liquids in the Aza-Michael Reaction: From Early Imidazolium Salts to Bio-Based Catalytic Media

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