On the public citation graph
Ruthenium-Catalyzed Synthesis of 5-Amino-1,2,3-triazole-4-carboxylates for Triazole-Based Scaffolds: Beyond the Dimroth Rearrangement
0 signed · 98 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known work and none has been retracted — and get a dated CiteStamped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/adsc.200600404openalex-snapshot
Copper Salt‐Catalyzed Azide‐[3 + 2] Cycloadditions of Ynamides and Bis‐Ynamides
inferredcites →https://doi.org/10.1002/anie.200805900openalex-snapshot
Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor with Conformationally Homogeneous Triazole‐Modified Cyclic Tetrapeptides
inferredcites →https://doi.org/10.1002/anie.200806390openalex-snapshot
Metal‐Free, Regioselective Triazole Ligations that Deliver Locked cis Peptide Mimetics
inferredcites →https://doi.org/10.1002/cber.19600930914openalex-snapshot
Synthesen stickstoffhaltiger Heterocyclen, XXIV. Darstellung und ortho‐Kondensation einiger 4.5‐disubstituierter 1.2.3‐Triazole
inferredcites →https://doi.org/10.1002/cber.19841170214openalex-snapshot
Heterocyclische β‐Enaminoester, 311). Neue 6:7‐, 6:8‐ und 5:6:7‐Kombinationen heterokondensierter Pyrimidine aus den Iminophosphoranen heterocyclischer β‐Enaminoester. – Stabile heterocyclische Ylide
inferredcites →https://doi.org/10.1002/chem.201100447openalex-snapshot
Microwave‐Assisted Aminocarbonylation of Ynamides by Using Catalytic [Fe3(CO)12] at Low Pressures of Carbon Monoxide
inferredcites →https://doi.org/10.1002/chin.200643041openalex-snapshot
Copper(II)‐Catalyzed Amidations of Alkynyl Bromides as a General Synthesis of Ynamides and (Z)‐Enamides. An Intramolecular Amidation for the Synthesis of Macrocyclic Ynamides.
inferredcites →https://doi.org/10.1002/cmdc.200800246openalex-snapshot
Peptides and Peptide Mimics as Modulators of Apoptotic Pathways
inferredcites →https://doi.org/10.1002/ejoc.200500434openalex-snapshot
Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds
inferredcites →https://doi.org/10.1002/ejoc.201100157openalex-snapshot
1,2,3‐Triazoles in Peptidomimetic Chemistry
inferredcites →https://doi.org/10.1002/ejoc.201301054openalex-snapshot
Experimental and Computational Investigation of the 1,3‐Dipolar Cycloaddition of the Ynamide tert‐Butyl N‐Ethynyl‐N‐phenylcarbamate with C‐Carboxymethyl‐N‐phenylnitrilimine
inferredcites →https://doi.org/10.1002/jlac.1990199001152openalex-snapshot
Synthese neuer 8‐Azapurine
inferredcites →https://doi.org/10.1002/mrc.1260240914openalex-snapshot
Heterocyclic β‐enamino esters 43—easy 13C NMR distinction between aryl‐substituted dimroth isomers of the 1,2,3‐triazole series
inferredcites →https://doi.org/10.1007/7081_2011_68openalex-snapshot
Recent Developments in the Synthesis 1,4,5-Trisubstituted Triazoles
inferredcites →https://doi.org/10.1016/j.bmcl.2011.08.085openalex-snapshot
Discovery of pyrazoles as novel FPR1 antagonists
inferredcites →https://doi.org/10.1016/j.tet.2007.06.008openalex-snapshot
1-Protected 5-amido 1,2,3-triazoles via ruthenium-catalyzed [3+2] cycloaddition of azides and ynamides
inferredcites →https://doi.org/10.1016/j.tet.2013.11.003openalex-snapshot
Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles via coupling reaction of diaminomaleonitrile with aromatic diazonium salts
inferredcites →https://doi.org/10.1016/j.tetlet.2008.01.071openalex-snapshot
Highly efficient synthesis of fused bicyclic 2,3-diaryl-pyrimidin-4(3H)-ones via Lewis acid assisted cyclization reaction
inferredcites →https://doi.org/10.1016/s0065-2725(10)01005-6openalex-snapshot
Recent Advances in the Dimroth Rearrangement
inferredcites →https://doi.org/10.1021/ar8000052openalex-snapshot
The Practice of Ring Constraint in Peptidomimetics Using Bicyclic and Polycyclic Amino Acids
inferredcites →https://doi.org/10.1021/cr100003sopenalex-snapshot
Ynamides: A Modern Functional Group for the New Millennium
inferredcites →https://doi.org/10.1021/ja01603a033openalex-snapshot
Metabolite Analogs. VI. Preparation of Some Analogs of 4-Amino-5-imidazole-carboxamide1
inferredcites →https://doi.org/10.1021/ja0749993openalex-snapshot
Ruthenium-Catalyzed Azide−Alkyne Cycloaddition: Scope and Mechanism
inferredcites →https://doi.org/10.1021/ja075865sopenalex-snapshot
Protein Prosthesis: 1,5-Disubstituted[1,2,3]triazoles as cis-Peptide Bond Surrogates
inferredcites →https://doi.org/10.1021/jm201155eopenalex-snapshot
Novel 3,4-Isoxazolediamides as Potent Inhibitors of Chaperone Heat Shock Protein 90
inferredcites →https://doi.org/10.1021/jm401536bopenalex-snapshot
Synthesis and Evaluation of New Hsp90 Inhibitors Based on a 1,4,5-Trisubstituted 1,2,3-Triazole Scaffold
inferredcites →https://doi.org/10.1021/jm801491wopenalex-snapshot
Conformationally Constrained Peptidomimetic Inhibitors of Signal Transducer and Activator of Transcription 3: Evaluation and Molecular Modeling
inferredcites →https://doi.org/10.1021/jo00798a035openalex-snapshot
Nonbridgehead fused nitrogen heterocycles. Fused 1,2,3-triazoles
inferredcites →https://doi.org/10.1021/jo01357a018openalex-snapshot
Synthesis and Isomerization of Substituted 5-Amino-1,2,3-triazoles1
inferredcites →https://doi.org/10.1021/jo0515226openalex-snapshot
Conformationally Constrained β-Amino Acid Derivatives by Intramolecular [2 + 2]-Photocycloaddition of a Tetronic Acid Amide and Subsequent Lactone Ring Opening
inferredcites →https://doi.org/10.1021/jo060230hopenalex-snapshot
Copper(II)-Catalyzed Amidations of Alkynyl Bromides as a General Synthesis of Ynamides and Z-Enamides. An Intramolecular Amidation for the Synthesis of Macrocyclic Ynamides
inferredcites →https://doi.org/10.1021/jo061688mopenalex-snapshot
A Study of the Scope and Regioselectivity of the Ruthenium-Catalyzed [3 + 2]-Cycloaddition of Azides with Internal Alkynes
inferredcites →https://doi.org/10.1021/jo802052jopenalex-snapshot
Synthesis of Conformationally Constrained Peptidomimetics using Multicomponent Reactions
inferredcites →https://doi.org/10.1021/jo900679copenalex-snapshot
Straightforward Stereoselective Access to Cyclic Peptidomimetics
inferredcites →https://doi.org/10.1021/jo972020yopenalex-snapshot
A Study on the Activation of Carboxylic Acids by Means of 2-Chloro-4,6-dimethoxy-1,3,5-triazine and 2-Chloro-4,6-diphenoxy-1,3,5-triazine
inferredcites →https://doi.org/10.1021/ol703077gopenalex-snapshot
Synthesis of Functionalized Oxazolones by a Sequence of Cu(II)- and Au(I)-Catalyzed Transformations
inferredcites →https://doi.org/10.1039/b606680aopenalex-snapshot
Tandem azidination– and hydroazidination–Huisgen [3 + 2] cycloadditions of ynamides. Synthesis of chiral amide-substituted triazoles
inferredcites →https://doi.org/10.1039/b701040kopenalex-snapshot
A triazole-templated ring-closing metathesis for constructing novel fused and bridged triazoles
inferredcites →https://doi.org/10.1039/b701444aopenalex-snapshot
Peptidomimetics via copper-catalyzed azide–alkyne cycloadditions
inferredcites →https://doi.org/10.1039/c0cs00218fopenalex-snapshot
Minimalist and universal peptidomimetics
inferredcites →https://doi.org/10.1039/ct9232300265openalex-snapshot
XXXIV.—2 : 5-Iminodihydro-1 : 2 : 3-triazole. Part I. Constitution of Dimroth's 5-anilinotriazole
inferredcites →https://doi.org/10.1039/p19730001629openalex-snapshot
1,2,3-Triazoles. Part I. Some 4-aminotriazole-5-carbaldehydes
inferredcites →https://doi.org/10.1055/s-2000-6490openalex-snapshot
4-(4,6-Dimethoxy[1,3,5]triazin-2-yl)-4-methyl-morpholinium Chloride (DMTMM): A Valuable Alternative to PyBOP for Solid Phase Peptide Synthesis
inferredcites →https://doi.org/10.1080/00397910500503595openalex-snapshot
Chiral (S)‐(+) 1‐Substituted Aryl‐4‐(1‐phenyl) Ethylformamido‐5‐amino‐1,2,3‐triazole: A New Class of Chiral Ligands for the Silver(I)‐Promoted Enantioselective Allylation of Aldehydes
inferredcites →https://doi.org/10.1080/00397911.2010.535940openalex-snapshot
New Efficient Synthesis of 5,6-Disubstituted-3-phenyl-1,2,3-triazolo[4,5-d]pyrimidin-7-ones via a Tandem Aza-Wittig Reaction
inferredcites →https://doi.org/10.2174/138527208786241501openalex-snapshot
Recent Progress of Synthetic Studies to Peptide and Peptidomimetic Cyclization
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.4755080openalex-extracted
Visible-Light-Induced Photocatalytic Iododi(Per)Fluoroalkylationof 5-Amino-N-Allyl-1,2,3-Triazole-4-Carboxamides
inferred← citeshttps://doi.org/10.1002/9783527694174.ch2openalex-snapshot
Applications of Click Chemistry in Drug Discovery and Development
inferred← citeshttps://doi.org/10.1002/adsc.201900791openalex-snapshot
An Atom‐Economical Approach to 2‐Triazolyl Thio‐/Seleno Pyridines via Ruthenium‐Catalyzed One‐pot [3+2]/[2+2+2] Cycloadditions
inferred← citeshttps://doi.org/10.1002/adsc.70096openalex-snapshot
Ruthenium‐Catalyzed Azide‐Selenoalkyne Cycloadditions: A Combined Synthetic–Computational Study into Reaction Scope, Mechanism, and Origins of Regioselectivity
inferred← citeshttps://doi.org/10.1002/ajoc.202000486openalex-snapshot
Transition Metal‐Catalyzed Cycloaddition of Azides with Internal Alkynes
inferred← citeshttps://doi.org/10.1002/asia.202400845openalex-snapshot
Divergent Regioselective Synthesis of Functionalized 1,2,3‐1H‐Triazoles from Nitriles and Arylazides Under Metal‐Free and/or Solvent‐Free Conditions
inferred← citeshttps://doi.org/10.1002/chin.201529187openalex-snapshot
ChemInform Abstract: Ruthenium‐Catalyzed Synthesis of 5‐Amino‐1,2,3‐triazole‐4‐carboxylates for Triazole‐Based Scaffolds: Beyond the Dimroth Rearrangement.
inferred← citeshttps://doi.org/10.1002/cjoc.70232openalex-snapshot
Copper(I)‐Catalyzed Interrupted Click/Amidation: Regioselective Synthesis of 5‐Amide‐1,2,3‐triazoles
inferred← citeshttps://doi.org/10.1002/cmdc.202300077openalex-snapshot
Ruthenium‐Catalyzed Cycloaddition for Introducing Chemical Diversity in Second‐Generation β‐Lactamase Inhibitors
inferred← citeshttps://doi.org/10.1002/ejoc.202000938openalex-snapshot
Transition‐Metal‐Free Annulation of Enamines and Tosyl Azide toward N‐Heterocycle Fused and 5‐Amino‐1,2,3‐Triazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202101559openalex-snapshot
One‐Pot Synthesis of 8‐Azaguanines by Transition Metal‐Free Cascade Cyclization of Carbodiimides with Ethyl Diazoacetate
inferred← citeshttps://doi.org/10.1002/ejoc.202401273openalex-snapshot
Divergent Synthesis of 4‐Aminotriazoles Through Click Cycloaddition and Generation of Iodonium(III) Triazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202501094openalex-snapshot
Push–Pull Ynamines and Push–Pull Ynamides: Synthesis, Structure, Reactivity, and Application
inferred← citeshttps://doi.org/10.1007/7081_2026_106openalex-snapshot
Click Chemistry for Peptidomimetic Applications
inferred← citeshttps://doi.org/10.1007/s13738-026-03607-7openalex-snapshot
Synthesis and evaluation of the anticancer activity and DNA binding properties of a 1,2,3-triazole compound and its Schiff base derivative
inferred← citeshttps://doi.org/10.1016/b978-0-08-100755-6.00008-9openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-820586-0.00008-xopenalex-snapshot
Advances in greener processes for triazole synthesis via azide-alkyne cycloaddition reactions
inferred← citeshttps://doi.org/10.1016/j.ccr.2016.02.010openalex-snapshot
Metal-catalyzed azide-alkyne “click” reactions: Mechanistic overview and recent trends
inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213217openalex-snapshot
A decade of advances in the reaction of nitrogen sources and alkynes for the synthesis of triazoles
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2024.110292openalex-snapshot
Visible-light-induced photocatalytic iododi(per)fluoroalkylation of 5-amino-N-allyl-1,2,3-triazole-4-carboxamides
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.129899openalex-snapshot
Coumarin-triazole hybrids: Design, microwave-assisted synthesis, crystal and molecular structure, theoretical and computational studies and screening for their anticancer potentials against PC-3 and DU-145
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145483openalex-snapshot
NN-type 1,2,3-triazole ligands and their transition metal complexes: Synthesis, structure, and DNA binding
inferred← citeshttps://doi.org/10.1016/j.tet.2017.08.029openalex-snapshot
Application of oxa-aza[3.3.3]propellanes in the diastereoselective synthesis of indeno[1,2-b]pyrroles bearing bistriazole unit
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.10.033openalex-snapshot
An efficient regioselective copper-catalyzed approach to the synthesis of 1,2,3-triazoles from N-tosylhydrazones and azides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00466openalex-snapshot
Ruthenium-Catalyzed Azide Alkyne Cycloaddition Reaction: Scope, Mechanism, and Applications
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02149openalex-snapshot
Synthesis of 4- and 5-Aminotriazolamers via Iterative Electrophilic Ethynylation and Azide–Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03944openalex-snapshot
Transition-Metal-Free Base-Promoted Divergent Synthesis of 5-Amide-1,2,3-triazole and 5-Imide-1,2,3-triazole Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03123openalex-snapshot
Iridium-Catalyzed Highly Regioselective Azide–Ynamide Cycloaddition to Access 5-Amido Fully Substituted 1,2,3-Triazoles under Mild, Air, Aqueous, and Bioorthogonal Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02089openalex-snapshot
Solvent-Directed Click Reaction between Active Methylene Compounds and Azido-1,3,5-triazines
inferred← citeshttps://doi.org/10.1021/acscatal.7b02558openalex-snapshot
Rhodium-Catalyzed Azide–Alkyne Cycloaddition of Internal Ynamides: Regioselective Assembly of 5-Amino-Triazoles under Mild Conditions
inferred← citeshttps://doi.org/10.1038/s41557-024-01442-yopenalex-snapshot
Protein-templated ligand discovery via the selection of DNA-encoded dynamic libraries
inferred← citeshttps://doi.org/10.1039/c7cc09934gopenalex-snapshot
Copper-catalyzed decarboxylative regioselective synthesis of 1,5-disubstituted 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/c7gc00901aopenalex-snapshot
Microwave-assisted solid phase diazotation: a method for the environmentally benign synthesis of benzotriazoles
inferred← citeshttps://doi.org/10.1039/d0cs00283fopenalex-snapshot
Reactivity of ynamides in catalytic intermolecular annulations
inferred← citeshttps://doi.org/10.1039/d0ob00168fopenalex-snapshot
Chiral 1,5-disubstituted 1,2,3-triazoles – versatile tools for foldamers and peptidomimetic applications
inferred← citeshttps://doi.org/10.1039/d0ob00579gopenalex-snapshot
Chemo- and regioselective click reactions through nickel-catalyzed azide–alkyne cycloaddition
inferred← citeshttps://doi.org/10.1039/d0qo01288bopenalex-snapshot
Transition-metal-free synthesis of 5-amino-1,2,3-triazoles via nucleophilic addition/cyclization of carbodiimides with diazo compounds
inferred← citeshttps://doi.org/10.1039/d2cc06708kopenalex-snapshot
Base-mediated ketenimine formation from N -sulfonylthioimidates for the synthesis of 5-amino-1-vinyl/aryl-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/d2ob02082copenalex-snapshot
Iridium-catalysed thioether-directed regioselective cycloaddition of internal alkynes with azides
inferred← citeshttps://doi.org/10.1039/d3ra00139copenalex-snapshot
Ring forming transformations of ynamides via cycloaddition
inferred← citeshttps://doi.org/10.1055/a-2216-4765openalex-snapshot
Base-Promoted [3+2] Annulation of Carbodiimides with Diazoacetonitrile for Synthesis of 5-Amino-4-cyano-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1055/s-0041-1737336openalex-snapshot
The Use of Propargylamines to Synthesize Amino-1,2,3-triazoles via Cycloaddition of Azides with Allenamines
inferred← citeshttps://doi.org/10.1055/sos-sd-235-00118openalex-snapshot
3 Ruthenium-Catalyzed Azide–Alkyne Cycloaddition (RuAAC)
inferred← citeshttps://doi.org/10.1080/00958972.2026.2649328openalex-snapshot
1,2,3-Triazole ligand and its Cu(II), Zn(II), Pt(II), Ru(II) complexes: synthesis, anticancer and antibacterial properties
inferred← citeshttps://doi.org/10.1080/10406638.2020.1757473openalex-snapshot
Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles Through a One-Pot Three Component Reaction of Boronic Acids, Sodium Azide and Active Methylene Compounds Under Ball-Milling Conditions
inferred← citeshttps://doi.org/10.1080/14756366.2019.1636044openalex-snapshot
Synthesis, activity evaluation, and pro-apoptotic properties of novel 1,2,4-triazol-3-amine derivatives as potent anti-lung cancer agents
inferred← citeshttps://doi.org/10.1515/hc-2022-0174openalex-snapshot
Synthetic and therapeutic review of triazoles and hybrids
inferred← citeshttps://doi.org/10.2174/1570179420666230418123350openalex-snapshot
Recent Progress on Synthesis of Functionalized 1,5-Disubstituted Triazoles
inferred← citeshttps://doi.org/10.3390/molecules27061999openalex-snapshot
General Method of Synthesis of 5-(Het)arylamino-1,2,3-triazoles via Buchwald–Hartwig Reaction of 5-Amino- or 5-Halo-1,2,3-triazoles
inferred← citeshttps://doi.org/10.3987/com-15-13371openalex-snapshot
Catalytic Cyclization of 2,3-Dibromopropionates with Benzyl Azides to Afford 1-Benzyl-1,2,3-triazole-4-carboxylate: The Use of a Nontoxic Bismuth Catalyst
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.