On the public citation graph
Unprecedented Cu(I)-Catalyzed Microwave-Assisted Three-Component Coupling of a Ketone, an Alkyne, and a Primary Amine
0 signed · 132 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2535::aid-anie2535>3.0.co;2-mopenalex-snapshot
Enantioselective Synthesis of Propargylamines by Copper-Catalyzed Addition of Alkynes to Enamines
inferredcites →https://doi.org/10.1002/adsc.200800232openalex-snapshot
Copper‐Catalyzed Four‐Component Coupling between Aldehydes, Amines, Alkynes, and Carbon Dioxide
inferredcites →https://doi.org/10.1002/anie.200900160openalex-snapshot
Addition–Hydroamination Reactions of Propargyl Cyanamides: Rapid Access to Highly Substituted 2‐Aminoimidazoles
inferredcites →https://doi.org/10.1002/chem.200501233openalex-snapshot
Practical Highly Enantioselective Synthesis of Propargylamines through a Copper‐Catalyzed One‐Pot Three‐Component Condensation Reaction
inferredcites →https://doi.org/10.1002/chem.200903143openalex-snapshot
Efficient Microwave‐Assisted Synthesis of Secondary Alkylpropargylamines by Using A3‐Coupling with Primary Aliphatic Amines
inferredcites →https://doi.org/10.1002/chin.200531066openalex-snapshot
An Efficient Synthesis of Propargylamines via C—H Activation Catalyzed by Copper(I) in Ionic Liquids.
inferredcites →https://doi.org/10.1002/qsar.200420034openalex-snapshot
Microwave‐assisted Cu (I) Catalyzed Solvent‐free Three Component Coupling of Aldehyde, Alkyne and Amine
inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.138openalex-snapshot
Enantioselective addition of phenyl and alkyl acetylenes to imines catalyzed by chiral Cu(I) complexes
inferredcites →https://doi.org/10.1016/s0040-4039(03)01674-5openalex-snapshot
Lewis acid promoted alkynylation of imines with terminal alkynes: simple, mild and efficient preparation of propargylic amines
inferredcites →https://doi.org/10.1016/s0040-4039(98)00639-xopenalex-snapshot
The solid phase synthesis of complex propargylamines using the combination of sonogashira and mannich reactions
inferredcites →https://doi.org/10.1021/cc700159uopenalex-snapshot
Formation of Substituted Pyrroles via an Imine Condensation/Aza-Claisen Rearrangement/Imine−Allene Cyclization Process by MAOS
inferredcites →https://doi.org/10.1021/ja00056a051openalex-snapshot
Highly selective and operationally simple synthesis of enantiomerically pure .beta.-amino esters via double stereodifferentiation
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/jm00080a013openalex-snapshot
Phenyl-substituted analogs of oxotremorine as muscarinic antagonists
inferredcites →https://doi.org/10.1021/jo00111a016openalex-snapshot
Lithium Alkoxides of Cinchona Alkaloids as Chiral Controllers for Enantioselective Acetylide Addition to Cyclic N-Acyl Ketimines
inferredcites →https://doi.org/10.1021/jo0480895openalex-snapshot
BF3-Mediated Additions of Organolithiums to Ketimines: X-ray Crystal Structures of BF3−Ketimine Complexes
inferredcites →https://doi.org/10.1021/jo052481gopenalex-snapshot
Very Mild, Enantioselective Synthesis of Propargylamines Catalyzed by Copper(I)−Bisimine Complexes
inferredcites →https://doi.org/10.1021/jo801290jopenalex-snapshot
Diversity Oriented Microwave-Assisted Synthesis of (−)-Steganacin Aza-Analogues
inferredcites →https://doi.org/10.1021/ol006321xopenalex-snapshot
An Efficient Chiral Moderator Prepared from Inexpensive (+)-3-Carene: Synthesis of the HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor DPC 963
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/ol035781yopenalex-snapshot
The First Silver-Catalyzed Three-Component Coupling of Aldehyde, Alkyne, and Amine
inferredcites →https://doi.org/10.1021/ol0526165openalex-snapshot
Enantioselective Addition of Terminal Alkynes to Isolated Isoquinoline Iminiums
inferredcites →https://doi.org/10.1021/ol060793fopenalex-snapshot
Enantioselective One-Pot Three-Component Synthesis of Propargylamines
inferredcites →https://doi.org/10.1023/b:modi.0000006822.51884.e6openalex-snapshot
Microwave-assisted Mannich-type three-component reactions
inferredcites →https://doi.org/10.1039/b409951fopenalex-snapshot
Practical highly enantioselective synthesis of terminal propargylamines. An expeditious synthesis of (S)-(+)-coniine
inferredcites →https://doi.org/10.1039/b416268dopenalex-snapshot
An efficient synthesis of propargylamines via C–H activation catalyzed by copper( i ) in ionic liquids
inferredcites →https://doi.org/10.1039/b507810eopenalex-snapshot
2-Phenallyl as a versatile protecting group for the asymmetric one-pot three-component synthesis of propargylamines
inferredcites →https://doi.org/10.1039/b607986popenalex-snapshot
Direct addition of alkynes to imines and related CN electrophiles: A convenient access to propargylamines
inferredcites →https://doi.org/10.1246/cl.2007.1422openalex-snapshot
Copper(I)- and Gold(I)-catalyzed Synthesis of 2,4-Disubstituted Quinoline Derivatives from N-Aryl-2-propynylamines
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/10.1002/9780471264194.fos02911.pub5openalex-snapshot
Copper( I ) Iodide
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02911.pub6openalex-snapshot
Copper( I ) Iodide
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02911.pub7openalex-snapshot
Copper( I ) Iodide
inferred← citeshttps://doi.org/10.1002/9781118863992.ch3openalex-snapshot
Metal‐Catalyzed Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/9783527647828.ch6openalex-snapshot
Literature Survey Part B: Miscellaneous Organic Transformations
inferred← citeshttps://doi.org/10.1002/9783527677894.ch9openalex-snapshot
Catalytic Nucleophilic Addition of Alkynes to Imines: The A 3 (Aldehyde–Alkyne–Amine) Coupling
inferred← citeshttps://doi.org/10.1002/9783527826445.ch10openalex-snapshot
Cu ‐Catalyzed Multicomponent Reactions
inferred← citeshttps://doi.org/10.1002/9783527826445.ch7openalex-snapshot
Microwave‐Assisted Cu ‐Catalyzed Organic Reactions
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/adsc.201200905openalex-snapshot
Cationic Gold‐ and Silver‐Catalyzed Cycloisomerizations of Propargylic Ureas: A Selective Entry to Oxazolidin‐2‐imines and Imidazolidin‐2‐ones
inferred← citeshttps://doi.org/10.1002/adsc.201300888openalex-snapshot
Copper‐Catalyzed Diversity‐Oriented Three‐ and Five‐ Component Synthesis of Mono‐ and Dipropargylic Amines via Coupling of Alkynes, α‐Amino Esters and Aldehydes
inferred← citeshttps://doi.org/10.1002/adsc.201300937openalex-snapshot
A Unique Route to Tetrasubstituted Propargylic Amines by Catalytic Markovnikov Hydroamination–Alkynylation
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/ajoc.202000460openalex-snapshot
Zinc Oxide Sensitized Graphene Quantum Dots “ZnO‐GQDs”: A Hybrid Concept to Study Charge Transfer and its Catalytic Applicability to Synthesize Tetrasubstituted Propargylamines
inferred← citeshttps://doi.org/10.1002/ajoc.202200023openalex-snapshot
Modern Development in Copper‐ and Nickel‐Catalyzed Cross‐Coupling Reactions: Formation of Carbon‐Carbon and Carbon‐Heteroatom bonds under Microwave Irradiation Conditions
inferred← citeshttps://doi.org/10.1002/ange.201206674openalex-snapshot
Copper/Titanium Catalysis Forms Fully Substituted Carbon Centers from the Direct Coupling of Acyclic Ketones, Amines, and Alkynes
inferred← citeshttps://doi.org/10.1002/ange.201209312openalex-snapshot
Copper‐Catalyzed Direct Secondary and Tertiary CH Alkylation of Azoles through a Heteroarene–Amine–Aldehyde/Ketone Coupling Reaction
inferred← citeshttps://doi.org/10.1002/ange.201400557openalex-snapshot
Chemoselective Amination of Propargylic C(sp3)H Bonds by Cobalt(II)‐Based Metalloradical Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202215741openalex-snapshot
Cadmium‐Doped and Pincer Ligand‐Modified Gold Nanocluster for Catalytic KA 2 Reaction
inferred← citeshttps://doi.org/10.1002/anie.201206674openalex-snapshot
Copper/Titanium Catalysis Forms Fully Substituted Carbon Centers from the Direct Coupling of Acyclic Ketones, Amines, and Alkynes
inferred← citeshttps://doi.org/10.1002/anie.201209312openalex-snapshot
Copper‐Catalyzed Direct Secondary and Tertiary CH Alkylation of Azoles through a Heteroarene–Amine–Aldehyde/Ketone Coupling Reaction
inferred← citeshttps://doi.org/10.1002/anie.201400557openalex-snapshot
Chemoselective Amination of Propargylic C(sp3)H Bonds by Cobalt(II)‐Based Metalloradical Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202215741openalex-snapshot
Cadmium‐Doped and Pincer Ligand‐Modified Gold Nanocluster for Catalytic KA 2 Reaction
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.5895openalex-snapshot
Choline chloride‐urea deep eutectic solvent as an efficient media for the synthesis of propargylamines via organocuprate intermediate
inferred← citeshttps://doi.org/10.1002/asia.201800567openalex-snapshot
Bifunctional Solid Catalyst for Organic Reactions in Water: Simultaneous Anchoring of Acetylacetone Ligands and Amphiphilic Ionic Liquid “Tags” by Using a Dihydropyran Linker
inferred← citeshttps://doi.org/10.1002/asia.202401058openalex-snapshot
N‐Heterocyclic Silylene‐Cu(I) Complexes as Efficient Catalysts for Three‐Component Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201103987openalex-snapshot
Mannich Reactions of Alkynes: Mechanistic Insights and the Role of Sub‐Stoichiometric Amounts of Alkynylcopper(I) Compounds in the Catalytic Cycle
inferred← citeshttps://doi.org/10.1002/chem.201301237openalex-snapshot
Rh‐Catalyzed Direct Enantioselective Alkynylation of α‐Ketiminoesters
inferred← citeshttps://doi.org/10.1002/chem.201504823openalex-snapshot
Identifying a Highly Active Copper Catalyst for KA2 Reaction of Aromatic Ketones
inferred← citeshttps://doi.org/10.1002/chin.201043061openalex-snapshot
ChemInform Abstract: Unprecedented Cu(I)‐Catalyzed Microwave‐Assisted Three‐Component Coupling of a Ketone, an Alkyne, and a Primary Amine.
inferred← citeshttps://doi.org/10.1002/cplu.202400765openalex-snapshot
Heteroleptic (NHC/MIC) Biscarbene Ag(I) and Au(I) Complexes: Synthesis, Characterization and Catalytic Applications
inferred← citeshttps://doi.org/10.1002/ejic.202300193openalex-snapshot
Correlating Structure and KA2 Catalytic Activity of ZnII Hydrazone Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201200090openalex-snapshot
Three‐Component Coupling of Aldehydes, Amines, and Alkynes Catalyzed by Oxidized Copper Nanoparticles on Titania
inferred← citeshttps://doi.org/10.1002/ejoc.201200990openalex-snapshot
CuI/SnCl2 Co‐Catalyzed Four‐Component Reaction of Ketones, Amines, Alkynes, and Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/ejoc.201402338openalex-snapshot
Copper(I)‐Catalyzed Decarboxylative Coupling of Propiolic Acids with Secondary Amines and Aldehydes
inferred← citeshttps://doi.org/10.1002/ejoc.201601103openalex-snapshot
Synthesis of Thiazolidine‐2‐thiones through a One‐Pot A3‐Coupling–Carbon Disulfide Incorporation Process
inferred← citeshttps://doi.org/10.1002/ejoc.201700603openalex-snapshot
Thiol–Yne Coupling of Propargylamine under Solvent‐Free Conditions by Bond Anion Relay Chemistry: An Efficient Synthesis of Thiazolidin‐2‐ylideneamine
inferred← citeshttps://doi.org/10.1002/ejoc.201701567openalex-snapshot
Zinc(II)‐Catalyzed Synthesis of Propargylamines by Coupling Aldimines and Ketimines with Alkynes
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/slct.201702268openalex-snapshot
Carbon Nitride‐Supported Silver Nanoparticles: Microwave‐ Assisted Synthesis of Propargylamine and Oxidative C‐C Coupling Reaction
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.201900024openalex-snapshot
Silver‐Mediated Organic Transformations of Propargylamines to Enones, α‐Thioketones, and Isochromans
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/s11030-024-10826-8openalex-snapshot
Synthesis of propargylamine: pioneering a green path with non-conventional KA2 coupling approach
inferred← citeshttps://doi.org/10.1007/s40010-024-00886-8openalex-snapshot
Synthesis and Application of Heterogeneous Zinc Catalysts for Decarboxylative Coupling
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11504-5openalex-snapshot
Catalytic Asymmetric 1,2-Alkynylation☆
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.04.019openalex-snapshot
Copper nanoparticles stabilized on nitrogen-doped carbon nanotubes as efficient and recyclable catalysts for alkyne/aldehyde/cyclic amine A3-type coupling reactions
inferred← citeshttps://doi.org/10.1016/j.catcom.2014.05.030openalex-snapshot
Highly efficient and scale-up synthesis of propargylamines catalyzed by graphene oxide-supported CuCl2 catalyst under microwave condition
inferred← citeshttps://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
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.inoche.2026.116397openalex-snapshot
A comprehensive review on the sustainable synthesis of indole-derived Schiff base ligands and their metal complexes for biological studies
inferred← citeshttps://doi.org/10.1016/j.molliq.2019.01.142openalex-snapshot
Ionic liquid assisted silver-catalyzed one-pot A3-coupling reactions for the synthesis of propargylamines
inferred← citeshttps://doi.org/10.1016/j.tet.2013.02.037openalex-snapshot
Unusual reactivity of 1-aminoanthraquinone in copper catalyzed multicomponent reaction with isatins and aryl alkynes: synthesis and photophysical properties of regioisomeric fluorescent 3-spiroheterocyclic 2-oxindoles
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134565openalex-snapshot
Recent advances in the syntheses and reactions of biologically promising β-lactam derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.063openalex-snapshot
Primary amine catalyzed electrophilic amination of α,α-disubstituted aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152083openalex-snapshot
Recent advances in copper-catalyzed imine-based multicomponent reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154987openalex-snapshot
Zinc-aluminum mixed oxide nanocomposites catalyzed KA2 coupling of ketone, amine, and an alkyne: An environmentally benign approach
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00343openalex-snapshot
Synthesis and Reactivity of Propargylamines in Organic Chemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01893openalex-snapshot
α-Tertiary Propargylamine Synthesis via KA2-Type Coupling Reactions under Solvent-Free CuI-Zeolite Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02127openalex-snapshot
Copper(I)-Catalyzed Ketone, Amine, and Alkyne Coupling for the Synthesis of 2-Alkynylpyrrolidines and -piperidines
inferred← citeshttps://doi.org/10.1021/acscatal.0c01212openalex-snapshot
Recent Progress on Catalytic Addition Reactions to N -Unsubstituted Imines
inferred← citeshttps://doi.org/10.1021/acsomega.1c03092openalex-snapshot
Zinc Iodide Catalyzed Synthesis of Trisubstituted Allenes from Terminal Alkynes and Ketones
inferred← citeshttps://doi.org/10.1021/acsomega.5c00134openalex-snapshot
New Prospects in the Inhibition of Monoamine Oxidase‑B (MAO-B) Utilizing Propargylamine Derivatives for the Treatment of Alzheimer’s Disease: A Review
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/acsomega.9b03428openalex-snapshot
Synthesis of Propargylamines via Michael Addition Using Methyl Vinyl Ketone Derivatives, 1-Alkynes, and Secondary Amines Catalyzed by Copper (I) Halides
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b00470openalex-snapshot
Cu(II)–Hydromagnesite Catalyzed Synthesis of Tetrasubstituted Propargylamines and Pyrrolo[1,2-a]quinolinesviaKA2, A3 Couplings and Their Decarboxylative Versions
inferred← citeshttps://doi.org/10.1021/jacs.6b01590openalex-snapshot
Mechanistic Studies and Expansion of the Substrate Scope of Direct Enantioselective Alkynylation of α-Ketiminoesters Catalyzed by Adaptable (Phebox)Rhodium(III) Complexes
inferred← citeshttps://doi.org/10.1021/jo2013725openalex-snapshot
Microwave-Assisted Decarboxylative Three-Component Coupling of a 2-Oxoacetic Acid, an Amine, and an Alkyne
inferred← citeshttps://doi.org/10.1021/jo500981ropenalex-snapshot
[Silver(I)(Pyridine-Containing Ligand)] Complexes As Unusual Catalysts for A3-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/ol2022164openalex-snapshot
Unprecedented Binary Cu(I)/Cu(II) Catalyzed One-Pot, Three-Component Synthesis and Evaluation of Luminescent Property of 2-Amino-3-iminoethenylidene-2-indolones: A New Class of Merocyanine Dye Analogues
inferred← citeshttps://doi.org/10.1021/ol3035609openalex-snapshot
Direct Catalytic Asymmetric Alkynylation of Ketoimines
inferred← citeshttps://doi.org/10.1021/ol502871ropenalex-snapshot
Base-Mediated Hydroamination of Propargylamine: A Regioselective Intramolecular 5- exo-dig Cycloisomerization en Route to Imidazole-2-thione
inferred← citeshttps://doi.org/10.1039/9781788016131-00343openalex-snapshot
Transition Metal-catalysed Nucleophilic Additions of Terminal Alkynes in Water: Development and Synthetic Utility
inferred← citeshttps://doi.org/10.1039/c0gc00807aopenalex-snapshot
“On water”-promoted direct alkynylation of isatins catalyzed by NHC–silver complexes for the efficient synthesis of 3-hydroxy-3-ethynylindolin-2-ones
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1039/c3cc45301dopenalex-snapshot
CuBr for KA2 reaction: en route to propargylic amines bearing a quaternary carbon center
inferred← citeshttps://doi.org/10.1039/c3gc36607copenalex-snapshot
Efficient three-component coupling catalysed by mesoporous copper–aluminum based nanocomposites
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1039/c3ob42221fopenalex-snapshot
Unexpected regio- and chemoselectivity of cationic gold-catalyzed cycloisomerizations of propargylureas: access to tetrasubstituted 3,4-dihydropyrimidin-2(1H)-ones
inferred← citeshttps://doi.org/10.1039/c4gc02318hopenalex-snapshot
Synthesis of tetrasubstituted propargylamines from cyclohexanone by solvent-free copper( ii ) catalysis
inferred← citeshttps://doi.org/10.1039/c4ra05190dopenalex-snapshot
Gold nanoparticle supported on ionic liquid-modified graphene oxide as an efficient and recyclable catalyst for one-pot oxidative A 3 -coupling reaction of benzyl alcohols
inferred← citeshttps://doi.org/10.1039/c4ra16005copenalex-snapshot
Facile and diverse microwave-assisted synthesis of secondary propargylamines in water using CuCl/CuCl 2
inferred← citeshttps://doi.org/10.1039/c5nj03272eopenalex-snapshot
Polystyrene supported N-phenylpiperazine–Cu( ii ) complex: an efficient and reusable catalyst for KA 2 -coupling reactions under solvent-free conditions
inferred← citeshttps://doi.org/10.1039/c6ra13371aopenalex-snapshot
Iodine-mediated regioselective guanylation-amination of propargylamines towards the synthesis of diversely substituted 2-aminoimidazoles
inferred← citeshttps://doi.org/10.1039/c6ra15857aopenalex-snapshot
Indirect conversion of ambient pressure CO 2 into oxazolidin-2-ones by a copper-based magnetic nanocatalyst
inferred← citeshttps://doi.org/10.1039/c6ra20767gopenalex-snapshot
Synthesis, structure and multifunctional catalytic properties of a Cu( i )-coordination polymer with outer-hanging CuBr 2
inferred← citeshttps://doi.org/10.1039/c7cs00065kopenalex-snapshot
Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles
inferred← citeshttps://doi.org/10.1080/07391102.2022.2163424openalex-snapshot
New2-((2-(2,4-dinitrophenyl)hydrazineeylidene) derivatives: design, synthesis, in silico , and in vitro anticancer studies
inferred← citeshttps://doi.org/10.1142/s1793604725500080openalex-snapshot
Structural regulation of CuOx/CeO2 and its application in α-tert-propylamine synthesis
inferred← citeshttps://doi.org/10.2174/1385272823666191113160643openalex-snapshot
Modern Catalysts in A3- Coupling Reactions
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/catal11010046openalex-snapshot
Recent Advances in Microwave-Assisted Copper-Catalyzed Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.3390/molecules25184043openalex-snapshot
Synthesis, Characterization, Catalytic Activity, and DFT Calculations of Zn(II) Hydrazone Complexes
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/10.3762/bjoc.11.154openalex-snapshot
Synthesis of alpha-tetrasubstituted triazoles by copper-catalyzed silyl deprotection/azide cycloaddition
inferred← citeshttps://doi.org/10.3762/bjoc.16.23openalex-snapshot
Combination of multicomponent KA2 and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones
inferred← citeshttps://doi.org/10.70675/cdca081fz1a31z453fz8cc3zae7c7b7d122aopenalex-snapshot
Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés
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.