On the public citation graph

The KA2 coupling reaction under green, solventless, heterogeneous catalysis

https://doi.org/10.1016/j.molcata.2016.09.028

0 signed · 69 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1098-2299(199711/12)42:3/4<150::aid-ddr6>3.0.co;2-popenalex-snapshot

Aliphatic propargylamines: New antiapoptotic drugs

inferredcites →https://doi.org/10.1002/adsc.201000914openalex-snapshot

Gold‐Catalyzed Direct Intermolecular Coupling of Ketones, Secondary Amines, and Alkynes: A Facile and Versatile Access to Propargylic Amines Containing a Quaternary Carbon Center

inferredcites →https://doi.org/10.1002/anie.200800098openalex-snapshot

Supported Gold(III) Catalysts for Highly Efficient Three‐Component Coupling Reactions

inferredcites →https://doi.org/10.1002/cjoc.200590266openalex-snapshot

Preferential Intercalation of Pyridinedicarboxylates into Layered Double Hydroxides

inferredcites →https://doi.org/10.1002/cjoc.200591076openalex-snapshot

Mercurous Chloride Catalyzed Mannich Condensation of Terminal Alkynes with Secondary Amines and Aldehydes

inferredcites →https://doi.org/10.1002/ejoc.201200090openalex-snapshot

Three‐Component Coupling of Aldehydes, Amines, and Alkynes Catalyzed by Oxidized Copper Nanoparticles on Titania

inferredcites →https://doi.org/10.1002/hlca.19870700310openalex-snapshot

Catalysis of Friedel‐Crafts Alkylation by a Montmorillonite Doped with Transition‐Metal Cations

inferredcites →https://doi.org/10.1016/j.catcom.2015.03.009openalex-snapshot

Cu2O/nano-CuFe2O4: A novel and recyclable magnetic catalyst for three-component coupling of carbonyl compounds–alkynes–amines under solvent-free condition

inferredcites →https://doi.org/10.1016/j.jcat.2011.10.013openalex-snapshot

Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand

inferredcites →https://doi.org/10.1016/j.molcata.2013.10.009openalex-snapshot

Nano-size ZnS: A novel, efficient and recyclable catalyst for A3-coupling reaction of propargylamines

inferredcites →https://doi.org/10.1016/j.tetlet.2008.09.026openalex-snapshot

Highly efficient three-component (aldehyde–alkyne–amine) coupling reactions catalyzed by a reusable PS-supported NHC–Ag(I) under solvent-free reaction conditions

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/jo500981ropenalex-snapshot

[Silver(I)(Pyridine-Containing Ligand)] Complexes As Unusual Catalysts for A3-Coupling Reactions

inferredcites →https://doi.org/10.1021/ol017022qopenalex-snapshot

Direct Addition of TMS-acetylene to Aldimines Catalyzed by a Simple, Commercially Available Ir(I) Complex

inferredcites →https://doi.org/10.1021/ol049936topenalex-snapshot

Microwave-Promoted Three-Component Coupling of Aldehyde, Alkyne, and Amine via C−H Activation Catalyzed by Copper in Water

inferredcites →https://doi.org/10.1021/ol060283lopenalex-snapshot

Reusable Polymer-Supported Catalyst for the [3+2] Huisgen Cycloaddition in Automation Protocols

inferredcites →https://doi.org/10.1039/b917923bopenalex-snapshot

Impregnated copper on magnetite: an efficient and green catalyst for the multicomponent preparation of propargylamines under solvent free conditions

inferredcites →https://doi.org/10.1039/c0ob00224kopenalex-snapshot

A simple method for the preparation of propargylamines using molecular sieve modified with copper(ii)

inferredcites →https://doi.org/10.1039/c2gc35604jopenalex-snapshot

Dual use of a chemical auxiliary: molecularly imprinted polymers for the selective recovery of products from biocatalytic reaction mixtures

inferredcites →https://doi.org/10.1039/c2gc35713eopenalex-snapshot

Copper(ii) catalysis provides cyclohexanone-derived propargylamines free of solvent or excess starting materials: sole by-product is water

inferredcites →https://doi.org/10.1039/c3cc45301dopenalex-snapshot

CuBr for KA2 reaction: en route to propargylic amines bearing a quaternary carbon center

inferredcites →https://doi.org/10.1039/c3cy00639eopenalex-snapshot

Efficient three-component coupling reactions catalyzed by Cu 0 -nanoparticles stabilized on modified montmorillonite

inferredcites →https://doi.org/10.1039/c3gc36607copenalex-snapshot

Efficient three-component coupling catalysed by mesoporous copper–aluminum based nanocomposites

inferredcites →https://doi.org/10.1039/c3nj01146aopenalex-snapshot

Nano copper( i ) oxide–zinc oxide catalyzed coupling of aldehydes or ketones, secondary amines, and terminal alkynes in solvent-free conditions

inferredcites →https://doi.org/10.1039/c5ra05468kopenalex-snapshot

Lanthanum loaded CuO nanoparticles: synthesis and characterization of a recyclable catalyst for the synthesis of 1,4-disubstituted 1,2,3-triazoles and propargylamines

inferredcites →https://doi.org/10.1039/c5ra05546fopenalex-snapshot

Unprecedented one-pot multicomponent synthesis of propargylamines using Amberlyst A-21 supported CuI under solvent-free conditions

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.4636655openalex-extracted

Probing the MAO Enzymes with a Novel Family of Quaternary Propargylamine Derivatives

inferred← citeshttps://doi.org/10.1002/adsc.201700535openalex-snapshot

Making Copper(0) Nanoparticles in Glycerol: A Straightforward Synthesis for a Multipurpose Catalyst

inferred← citeshttps://doi.org/10.1002/adsc.202000566openalex-snapshot

Manganese‐Catalyzed Multicomponent Synthesis of Tetrasubstituted Propargylamines: System Development and Theoretical Study

inferred← citeshttps://doi.org/10.1002/aoc.4669openalex-snapshot

A reusable polymer‐supported copper(I) catalyst for triazole click reaction on water: An experimental and computational study

inferred← citeshttps://doi.org/10.1002/aoc.5429openalex-snapshot

CuII@PAA/PVC mesoporous fibers: A hybrid wedding as a high‐performance versatile heterogeneous catalyst for A3, KA2, and decarboxylative A3 reactions

inferred← citeshttps://doi.org/10.1002/aoc.6109openalex-snapshot

Effective catalytic approach of NiTiO3 photosonocatalyst for the synthesis of indazolo[3,2‐b]quinazoline and its photophysical property

inferred← citeshttps://doi.org/10.1002/cplu.202400365openalex-snapshot

Silver Complex Bearing N‐Heterocyclic Carbene Bidentate Chelating Ligand as an Efficient Catalyst in Solvent‐Free KA2 Coupling

inferred← citeshttps://doi.org/10.1002/ejoc.201701033openalex-snapshot

The Synthesis of Group 10 and 11 Metal Complexes of 3,6,9‐Trithia‐1‐(2,6)‐pyridinacyclodecaphane and Their Use in A3‐Coupling Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.201800850openalex-snapshot

Transition‐Metal‐Free Addition of Acetylenes to Ketimines: the First Base‐Catalyzed Ethynylation of the C=N Bond

inferred← citeshttps://doi.org/10.1002/ejoc.202301095openalex-snapshot

KA2 Coupling, Catalyzed by Well‐Defined NHC‐Coordinated Copper(I): Straightforward and Efficient Construction of α‐Tertiary Propargylamines**

inferred← citeshttps://doi.org/10.1002/open.202200223openalex-snapshot

Propargyl Amines: Versatile Building Blocks in Post‐Ugi Transformations

inferred← citeshttps://doi.org/10.1002/slct.201801516openalex-snapshot

KA 2 ‐Coupling Reaction Catalyzed by Semi‐Heterogeneous Magnetically Graphene Oxide Supported Copper Catalyst under Microwave Condition

inferred← citeshttps://doi.org/10.1002/slct.201901729openalex-snapshot

Cu doped ZIF Catalyzed Synthesis of Propargyl Amines with Quaternary Carbon Center Under Solvent Free Conditions

inferred← citeshttps://doi.org/10.1002/slct.202505339openalex-snapshot

TIBAL‐Assisted Copper‐Catalyzed Ketone‐Amine‐Alkyne (KA 2 ) Reaction for Preparation of α‐Tertiary Propargylamines in Mild Conditions

inferred← citeshttps://doi.org/10.1007/s00289-021-03651-8openalex-snapshot

KA2 and A3 coupling reactions promoted by Fe3O4@T-CS@Cys@Ag+ nanocomposite

inferred← citeshttps://doi.org/10.1007/s10562-018-2449-6openalex-snapshot

[Zn(l-proline)2] Catalyzed One-Pot Synthesis of Propargylamines Under Solvent-Free Conditions

inferred← citeshttps://doi.org/10.1016/j.apcata.2017.07.006openalex-snapshot

Combining ethylenediamine and ionic liquid functionalities within SBA-15: A promising catalytic pair for tandem Cu–AAC reaction

inferred← citeshttps://doi.org/10.1016/j.arabjc.2020.09.053openalex-snapshot

Facile Amberlyst A-21 catalyzed access of β-hydroxynitriles via epoxide opening in water

inferred← citeshttps://doi.org/10.1016/j.carbpol.2019.115393openalex-snapshot

Cu-metal-organic framework supported on chitosan for efficient condensation of aromatic aldehydes and malononitrile

inferred← citeshttps://doi.org/10.1016/j.cclet.2019.11.004openalex-snapshot

1D Fe3O4@CuSiO3 composites catalyzed decarboxylative A3-coupling for propargylamine synthesis

inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213603openalex-snapshot

The Ketone-Amine-Alkyne (KA2) coupling reaction: Transition metal-catalyzed synthesis of quaternary propargylamines

inferred← citeshttps://doi.org/10.1016/j.ccr.2021.213827openalex-snapshot

Metal-organic framework composites as green/sustainable catalysts

inferred← citeshttps://doi.org/10.1016/j.cej.2018.05.046openalex-snapshot

Cooperative N-heterocyclic carbene Au and amino catalysis for continuous synthesis of secondary propargylamines in a fiber supported hydrophilic microenvironment

inferred← citeshttps://doi.org/10.1016/j.matchemphys.2018.10.057openalex-snapshot

Copper incorporated into 1H-1,2,3-triazole-5-methanol functionalized halloysite nano clay as an efficient and heterogeneous catalyst for promoting green A3 and KA2 coupling reaction: Optimization of reaction variables using response surface methodology

inferred← citeshttps://doi.org/10.1016/j.saa.2020.118327openalex-snapshot

Fluorescent detection of S2− based on ZnMOF-74 and CuMOF-74

inferred← citeshttps://doi.org/10.1016/j.tgchem.2023.100027openalex-snapshot

Tandem CuI – Zinc dust as a sustainable catalyst for the preparation of propargylamine derivatives via an A3 coupling reaction, under neat conditions

inferred← citeshttps://doi.org/10.1021/acsanm.2c02666openalex-snapshot

Hollow CuO–CeO2 Nanospheres for an Effectively Catalytic Annulation/A3-Coupling Reaction Sequence

inferred← citeshttps://doi.org/10.1021/acsomega.9b01387openalex-snapshot

Zn-Catalyzed Multicomponent KA2 Coupling: One-Pot Assembly of Propargylamines Bearing Tetrasubstituted Carbon Centers

inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b01754openalex-snapshot

Solvent-Free A3 and KA2 Coupling Reactions with mol ppm Level Loadings of a Polymer-Supported Copper(II)–Bipyridine Complex for Green Synthesis of Propargylamines

inferred← citeshttps://doi.org/10.1039/c7gc02038dopenalex-snapshot

A regioselective one-pot aza-Friedel–Crafts reaction for primary, secondary and tertiary anilines using a heterogeneous catalyst

inferred← citeshttps://doi.org/10.1039/c8nj01718bopenalex-snapshot

Synthesis and crystal structures of salen-type Cu( ii ) and Ni( ii ) Schiff base complexes: application in [3+2]-cycloaddition and A 3 -coupling reactions

inferred← citeshttps://doi.org/10.1039/d1ra03324gopenalex-snapshot

Solvent-free synthesis of propargylamines: an overview

inferred← citeshttps://doi.org/10.1039/d2ra07700kopenalex-snapshot

Stabilization of copper nanoparticles onto the double Schiff-base-functionalized ZSM-5 for A 3 coupling reaction catalysis aimed under mild conditions

inferred← citeshttps://doi.org/10.1155/2017/6267036openalex-snapshot

Solvent-Free Henry and Michael Reactions with Nitroalkanes Promoted by Potassium Carbonate as a Versatile Heterogeneous Catalyst

inferred← citeshttps://doi.org/10.2174/1385272827666230614151935openalex-snapshot

Catalysts For Propargylamines Synthesis Via A3, AHA, and KA2 Coupling - A Review

inferred← citeshttps://doi.org/10.3390/catal12070725openalex-snapshot

Recent Advances in Multicomponent Reactions Catalysed under Operationally Heterogeneous Conditions

inferred← citeshttps://doi.org/10.3390/molecules29112486openalex-snapshot

Are Terminal Alkynes Necessary for MAO-A/MAO-B Inhibition? A New Scaffold Is Revealed

inferred← citeshttps://doi.org/10.59761/rcr5145openalex-snapshot

Reaction of acetylenic carbanions with C=N bond: dynamics of development, synthetic divergence, environmental safety

inferred← citeshttps://doi.org/10.70675/656eb804ze63bz48a6z84b3z2178c6efbcbfopenalex-snapshot

(Bi)metallic nanoparticles in glycerol : synthesis, characterization and catalytic aplications

inferred← citeshttps://doi.org/10.7287/peerj.5065v0.1/reviews/1openalex-snapshot

Peer Review #1 of "One-pot multicomponent nitro-Mannich reaction using a heterogeneous catalyst under solvent-free conditions (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.5065v0.1/reviews/2openalex-snapshot

Peer Review #2 of "One-pot multicomponent nitro-Mannich reaction using a heterogeneous catalyst under solvent-free conditions (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.5065v0.1/reviews/3openalex-snapshot

Peer Review #3 of "One-pot multicomponent nitro-Mannich reaction using a heterogeneous catalyst under solvent-free conditions (v0.1)"

inferred← citeshttps://doi.org/10.7717/peerj.5065openalex-snapshot

One-pot multicomponent nitro-Mannich reaction using a heterogeneous catalyst under solvent-free conditions

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.