On the public citation graph

1,3-Dipolar cycloaddition of azides with electron-deficient alkynes under mild condition in water

https://doi.org/10.1016/j.tetlet.2004.02.089
0 signed · 187 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/1521-3773(20010401)40:7<1162::aid-anie1162>3.0.co;2-fopenalex-snapshot
Electrochemical Surface Science
inferredcites →https://doi.org/10.1002/1521-3773(20020315)41:6<1053::aid-anie1053>3.0.co;2-4openalex-snapshot
Click Chemistry In Situ: Acetylcholinesterase as a Reaction Vessel for the Selective Assembly of a Femtomolar Inhibitor from an Array of Building Blocks
inferredcites →https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4openalex-snapshot
A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
inferredcites →https://doi.org/10.1002/cber.19671000806openalex-snapshot
1.3‐Dipolare Cycloadditionen, XXXII. Kinetik der Additionen organischer Azide an CC‐Mehrfachbindungen
inferredcites →https://doi.org/10.1016/s0040-4020(01)81492-7openalex-snapshot
Synthesis and reactivity of methyl γ-azido butyrates and ethyl σ-azido valerates and of the corresponding acid chlorides as useful reagents for the aminoalkylation
inferredcites →https://doi.org/10.1021/ja01632a010openalex-snapshot
Synthesis of 4-Alkyl-V-triazoles from Acetylenic Compounds and Hydrogen Azide1
inferredcites →https://doi.org/10.1021/ja020887uopenalex-snapshot
Synthesis of Sugar Arrays in Microtiter Plate
inferredcites →https://doi.org/10.1021/ja034490hopenalex-snapshot
Activity-Based Protein Profiling in Vivo Using a Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
inferredcites →https://doi.org/10.1021/ja036765zopenalex-snapshot
Cell Surface Labeling of Escherichia coli via Copper(I)-Catalyzed [3+2] Cycloaddition
inferredcites →https://doi.org/10.1021/jo00100a019openalex-snapshot
Steric Effects on the Regioselectivity of an Azide-Alkyne Dipolar Cycloaddition Reaction: The Synthesis of Human Leukocyte Elastase Inhibitors
inferredcites →https://doi.org/10.1021/jo00168a070openalex-snapshot
Cycloaddition induced by cucurbituril. A case of Pauling principle catalysis
inferredcites →https://doi.org/10.1021/jo00283a024openalex-snapshot
Catalysis by cucurbituril. The significance of bound-substrate destabilization for induced triazole formation
inferredcites →https://doi.org/10.1021/jo011148jopenalex-snapshot
Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
inferredcites →https://doi.org/10.1021/jo026615ropenalex-snapshot
Click Chemistry to Construct Fluorescent Oligonucleotides for DNA Sequencing
inferredcites →https://doi.org/10.1039/b008175mopenalex-snapshot
Mainchain pseudopolyrotaxanes via post-threading with cucurbituril
inferredcites →https://doi.org/10.1039/b108519kopenalex-snapshot
Formation of oligotriazoles catalysed by cucurbituril
inferredcites →https://doi.org/10.1039/b109256copenalex-snapshot
The synthesis of [2], [3] and [4]rotaxanes and semirotaxanes
inferredcites →https://doi.org/10.1055/s-1990-26820openalex-snapshot
The Synthesis of Triazole Analogues of Antitumor Dehydropyrrolizidine Alkaloids
inferredcites →https://doi.org/10.1351/pac198961040613openalex-snapshot
Kinetics and reaction mechanisms: selected examples from the experience of forty years
inferredcites →https://doi.org/10.3987/com-93-6516openalex-snapshot
Synthesis of Diethyl 1,2,3-Triazolealkylphosphonates through 1,3-Dipolar Cycloaddition of Azides with Acetylenes
inferredcites →https://doi.org/10.3987/com-96-7585openalex-snapshot
Cycloaddition of Acetylenes with 5-Azido-5-deoxy-D-aldopentose Derivatives: Synthesis of Triazole Reversed Nucleoside Analogs

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.4674670openalex-extracted
Propiolic Based Copper Free Click Chemistry: A Promising Tool for Bioconjugation Onto Plla Surface
inferred← citeshttps://doi.org/10.1002/0471142700.nc0433s35openalex-snapshot
Synthesis of Alkyne‐ and Azide‐Modified Oligonucleotides and Their Cyclization by the CuAAC (Click) Reaction
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0924openalex-snapshot
Click Chemistry and Nitrogen‐Containing Heterocycles Formed in Surface Functionalization Reactions
inferred← citeshttps://doi.org/10.1002/9780470747957.ch7openalex-snapshot
Noncarbon Cumulenes
inferred← citeshttps://doi.org/10.1002/9780470825150.ch2openalex-snapshot
Ultrarapid Approaches to Mild Macromolecular Conjugation
inferred← citeshttps://doi.org/10.1002/9780470988817.ch5openalex-snapshot
Pericyclic Reactions in Aqueous Media
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11212.pub2openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11212.pub3openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11212.pub4openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11212.pub5openalex-snapshot
Water
inferred← citeshttps://doi.org/10.1002/9781118854754.ch2openalex-snapshot
Chemical Methodology for Labelling and Bioconjugation
inferred← citeshttps://doi.org/10.1002/9783527637737.ch12openalex-snapshot
Five‐Membered Heterocycles with Three Heteroatoms: Triazoles
inferred← citeshttps://doi.org/10.1002/9783527846849.ch7openalex-snapshot
Pericyclic Reactions in Aqueous Medium
inferred← citeshttps://doi.org/10.1002/adfm.201302847openalex-snapshot
Click Chemistry in Materials Science
inferred← citeshttps://doi.org/10.1002/adfm.201706046openalex-snapshot
Bioorthogonal Strategies for Engineering Extracellular Matrices
inferred← citeshttps://doi.org/10.1002/adsc.201100865openalex-snapshot
Click Functionalization of Gold Nanoparticles Using the Very Efficient Catalyst Copper(I) (Hexabenzyl)tris(2‐aminoethyl)‐ amine Bromide
inferred← citeshttps://doi.org/10.1002/adsc.201300343openalex-snapshot
An Abnormal N‐Heterocyclic Carbene–Copper(I) Complex in Click Chemistry
inferred← citeshttps://doi.org/10.1002/advs.202104012openalex-snapshot
Protein Nanoparticles: Uniting the Power of Proteins with Engineering Design Approaches
inferred← citeshttps://doi.org/10.1002/ange.200802077openalex-snapshot
Postsynthetische DNA‐Modifizierung mithilfe der kupferkatalysierten Azid‐Alkin‐Cycloaddition
inferred← citeshttps://doi.org/10.1002/ange.200900755openalex-snapshot
Klick‐Chemie jenseits von metallkatalysierten Cycloadditionen
inferred← citeshttps://doi.org/10.1002/ange.201101019openalex-snapshot
Zuverlässige und effiziente Konjugation von Biomolekülen über Huisgen‐Azid‐Alkin‐Cycloadditionen
inferred← citeshttps://doi.org/10.1002/ange.201101581openalex-snapshot
Bio‐orthogonal “Double‐Click” Chemistry Based on Multifunctional Coatings
inferred← citeshttps://doi.org/10.1002/ange.202501262openalex-snapshot
Electron‐Deficient Alkyne Lipids Enable Efficient Synthesis of Comparable Polymer Lipids via Copper‐Free Azide‐Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1002/anie.200802077openalex-snapshot
Postsynthetic DNA Modification through the Copper‐Catalyzed Azide–Alkyne Cycloaddition Reaction
inferred← citeshttps://doi.org/10.1002/anie.200900755openalex-snapshot
Click Chemistry beyond Metal‐Catalyzed Cycloaddition
inferred← citeshttps://doi.org/10.1002/anie.201101019openalex-snapshot
Reliable and Efficient Procedures for the Conjugation of Biomolecules through Huisgen Azide–Alkyne Cycloadditions
inferred← citeshttps://doi.org/10.1002/anie.201101581openalex-snapshot
Bio‐orthogonal “Double‐Click” Chemistry Based on Multifunctional Coatings
inferred← citeshttps://doi.org/10.1002/anie.202501262openalex-snapshot
Electron‐Deficient Alkyne Lipids Enable Efficient Synthesis of Comparable Polymer Lipids via Copper‐Free Azide‐Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1002/asia.201100404openalex-snapshot
Metal‐Free 1,5‐Regioselective Azide–Alkyne [3+2]‐Cycloaddition
inferred← citeshttps://doi.org/10.1002/cbdv.200790229openalex-snapshot
Synthesis of Oligonucleotides Carrying 5′‐5′ Linkages Using Copper‐Catalyzed Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1002/cbic.200700278openalex-snapshot
Metal‐Free Triazole Formation as a Tool for Bioconjugation
inferred← citeshttps://doi.org/10.1002/cbic.200900640openalex-snapshot
Covalent‐Bond‐Based Immobilization Approaches for Single‐Molecule Fluorescence
inferred← citeshttps://doi.org/10.1002/cbic.201000064openalex-snapshot
Azide: A Unique Dipole for Metal‐Free Bioorthogonal Ligations
inferred← citeshttps://doi.org/10.1002/chem.200600961openalex-snapshot
(NHC)Copper( I )‐Catalyzed [3+2] Cycloaddition of Azides and Mono‐ or Disubstituted Alkynes
inferred← citeshttps://doi.org/10.1002/chem.201003131openalex-snapshot
Catalyst‐Free Conjugation and In Situ Quantification of Nanoparticle Ligand Surface Density Using Fluorogenic Cu‐Free Click Chemistry
inferred← citeshttps://doi.org/10.1002/chem.201103093openalex-snapshot
Morphology‐Controlled Synthesis of Poly(oxyethylene)silicone or Alkylsilicone Surfactants with Explicit, Atomically Defined, Branched, Hydrophobic Tails
inferred← citeshttps://doi.org/10.1002/chem.201800834openalex-snapshot
Optically Functionalized Grid‐Type Complexes by a Post‐Assembly Strategy
inferred← citeshttps://doi.org/10.1002/chem.202000224openalex-snapshot
Gas–Solid Heterogeneous Postsynthetic Modification of Imine‐Based Covalent Organic Frameworks
inferred← citeshttps://doi.org/10.1002/ejoc.200500483openalex-snapshot
CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
inferred← citeshttps://doi.org/10.1002/ejoc.200901446openalex-snapshot
Unsupported Copper Nanoparticles in the 1,3‐Dipolar Cycloaddition of Terminal Alkynes and Azides
inferred← citeshttps://doi.org/10.1002/ejoc.201500685openalex-snapshot
Water‐Soluble Maleimide‐Modified Gold Nanoparticles (AuNPs) as a Platform for Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1002/ejoc.202101235openalex-snapshot
Controlling Selectivity in the Synthesis of Z‐α,β‐Unsaturated Amidines by Tuning the N‐Sulfonyl Group in a Rhodium(II) Catalyzed 1,2‐H Shift
inferred← citeshttps://doi.org/10.1002/hlca.200590134openalex-snapshot
Activation Energies and Reaction Energetics for 1,3‐Dipolar Cycloadditions of Hydrazoic Acid with CC and CN Multiple Bonds from High‐Accuracy and Density Functional Quantum Mechanical Calculations
inferred← citeshttps://doi.org/10.1002/macp.201800147openalex-snapshot
Copper‐Free Synthesis of Glycidyl Triazolyl Polymers
inferred← citeshttps://doi.org/10.1002/marc.200900924openalex-snapshot
Ultra Rapid Approaches to Mild Macromolecular Conjugation
inferred← citeshttps://doi.org/10.1002/marc.201300865openalex-snapshot
Covalently Linked Plasticizers: Triazole Analogues of Phthalate Plasticizers Prepared by Mild Copper‐Free “Click” Reactions with Azide‐Functionalized PVC
inferred← citeshttps://doi.org/10.1002/marc.201700070openalex-snapshot
Metal‐Free Poly‐Cycloaddition of Activated Azide and Alkynes toward Multifunctional Polytriazoles: Aggregation‐Induced Emission, Explosive Detection, Fluorescent Patterning, and Light Refraction
inferred← citeshttps://doi.org/10.1002/pi.2650openalex-snapshot
In situ crosslinked hydrogels formed using Cu(I)‐free Huisgen cycloaddition reaction
inferred← citeshttps://doi.org/10.1002/pol.20190088openalex-snapshot
Fabrication of polyurethane binders grafted with functional reactive plasticizers by a catalyst‐free click reaction
inferred← citeshttps://doi.org/10.1002/pola.26511openalex-snapshot
Highly efficient divergent synthesis of dendrimers via metal‐free “click” chemistry
inferred← citeshttps://doi.org/10.1002/prep.201500268openalex-snapshot
Reactive Energetic Plasticizers for Energetic Polyurethane Binders Prepared via Simultaneous Huisgen Azide‐Alkyne Cycloaddition and Polyurethane Reaction
inferred← citeshttps://doi.org/10.1002/prep.201700219openalex-snapshot
Synthesis and Characterization of New PGN Based Reactive Oligomeric Plasticizers for Glycidyl Azide Polymer
inferred← citeshttps://doi.org/10.1002/slct.201800266openalex-snapshot
Facile Solvent‐ and Metal‐Free Synthesis of Polymers Including Triazole by Click Reaction
inferred← citeshttps://doi.org/10.1002/slct.201901403openalex-snapshot
Amberlyst‐15‐catalyzed Procedure for the Synthesis of Novel 2,4‐Dihydroxybenzoyl‐1,2,3‐triazoles and Molecular Modelling Studies for Hsp‐90 Inhibition
inferred← citeshttps://doi.org/10.1007/10_2010_92openalex-snapshot
Engineering Liposomes and Nanoparticles for Biological Targeting
inferred← citeshttps://doi.org/10.1007/978-1-0716-2954-3_15openalex-snapshot
Click Chemistry for Liposome Surface Modification
inferred← citeshttps://doi.org/10.1007/978-1-4939-6591-5_8openalex-snapshot
Coupling of Ligands to the Liposome Surface by Click Chemistry
inferred← citeshttps://doi.org/10.1007/978-1-60327-360-2_18openalex-snapshot
Conjugation of Ligands to the Surface of Preformed Liposomes by Click Chemistry
inferred← citeshttps://doi.org/10.1007/s11095-008-9616-1openalex-snapshot
Click Chemistry, A Powerful Tool for Pharmaceutical Sciences
inferred← citeshttps://doi.org/10.1007/s40242-019-9077-6openalex-snapshot
Synthesis of PEGylated Salicylaldehyde Azine via Metal-free Click Chemistry for Cellular Imaging Applications
inferred← citeshttps://doi.org/10.1016/b978-0-08-096807-0.00008-7openalex-snapshot
Five-Membered Ring Systems: With More than One N Atom
inferred← citeshttps://doi.org/10.1016/b978-0-08-100262-9.00014-8openalex-snapshot
Click chemistry for improving properties of bioresorbable polymers for medical applications
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2018.06.021openalex-snapshot
Pretargeting in nuclear imaging and radionuclide therapy: Improving efficacy of theranostics and nanomedicines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2011.03.016openalex-snapshot
Synthesis and in vitro evaluation of [18F]fluoroethyl triazole labelled [Tyr3]octreotate analogues using click chemistry
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.008openalex-snapshot
Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds
inferred← citeshttps://doi.org/10.1016/j.carres.2025.109511openalex-snapshot
Microwave-assisted click synthesis of levoglucosan triazolyl glycoconjugates using ascorbyl palmitate sodium salt (Asp-Na) as a green Co-catalyst
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.06.028openalex-snapshot
The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview
inferred← citeshttps://doi.org/10.1016/j.crci.2010.05.025openalex-snapshot
Cycloaddition reactions in aqueous systems: A two-decade trend endeavor
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115338openalex-snapshot
Advances of bioorthogonal coupling reactions in drug development
inferred← citeshttps://doi.org/10.1016/j.elecom.2015.07.019openalex-snapshot
Two-step local functionalization of fluoropolymer Dyneon THV microfluidic materials by scanning electrochemical microscopy combined to click reaction
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2019.109414openalex-snapshot
Preparation of energetic polyurethane binders with enhanced properties by nonmigratory reactive monocyclic plasticizers
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2026.114584openalex-snapshot
Post-functionalization of α-anthracene-ω-azido poly(2-oxazoline)s: Chemoselectivity of metal-free Huisgen reaction versus Diels-Alder cycloaddition
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.127755openalex-snapshot
Chitosan-based oral hydrogel formulations of β-galactosidase to improve enzyme supplementation therapy for lactose intolerance
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2009.05.051openalex-snapshot
Influence of dialkyne structure on the properties of new click-gels based on hyaluronic acid
inferred← citeshttps://doi.org/10.1016/j.jcis.2007.09.054openalex-snapshot
Reagentless functionalization of gold nanoparticles via a 3 + 2 Huisgen cycloaddition
inferred← citeshttps://doi.org/10.1016/j.jct.2011.05.028openalex-snapshot
Vapor pressures and enthalpies of vaporization of azides
inferred← citeshttps://doi.org/10.1016/j.molcata.2006.04.054openalex-snapshot
Preparation of alumina supported copper nanoparticles and their application in the synthesis of 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.05.031openalex-snapshot
Structures of supramolecular assemblies formed by substituted cucurbiturils and metal ions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.01.035openalex-snapshot
Synthesis and characterization of [1,2,3]-triazole containing liquid crystals through click reaction
inferred← citeshttps://doi.org/10.1016/j.msec.2016.10.003openalex-snapshot
Novel electrospun nanofibers of modified gelatin-tyrosine in cartilage tissue engineering
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2019.05.012openalex-snapshot
Chemical cross-linking methods for cell encapsulation in hydrogels
inferred← citeshttps://doi.org/10.1016/j.nucmedbio.2009.05.001openalex-snapshot
In-depth evaluation of the cycloaddition–retro-Diels–Alder reaction for in vivo targeting with [111In]-DTPA-RGD conjugates
inferred← citeshttps://doi.org/10.1016/j.polymer.2015.04.004openalex-snapshot
Improved synthesis of bicyclic polystyrenes by ATRP and “click” reaction
inferred← citeshttps://doi.org/10.1016/j.polymer.2018.03.017openalex-snapshot
Indirect functionalization of multiwalled carbon nano tubes through non-covalent interaction of functional polyesters
inferred← citeshttps://doi.org/10.1016/j.polymer.2018.06.073openalex-snapshot
Surface-initiated RAFT polymerization from vapor-based polymer coatings
inferred← citeshttps://doi.org/10.1016/j.tet.2005.10.039openalex-snapshot
Synthesis of Fréchet type dendritic benzyl propargyl ether and Fréchet type triazole dendrimer
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.051openalex-snapshot
Facile and quick synthesis of 1-monosubstituted aryl 1,2,3-triazoles: a copper-free [3+2] cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tet.2013.04.093openalex-snapshot
Investigation of the lipase-catalysed reaction of aliphatic amines with ethyl propiolate as a route to N-substituted propiolamides
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.056openalex-snapshot
Synthesis of fused nine-membered rings: a simple protocol for synthesis of [1,2,3]-triazolo-[1,4]-benzoxazonine frameworks from the Baylis–Hillman acetates
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132445openalex-snapshot
Catalyst-free [3+2] cycloaddition of azodicarbonyls and -hydroxyaryl azomethine ylides on water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.03.007openalex-snapshot
Cu(I)-catalyzed one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles via nucleophilic displacement and 1,3-dipolar cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.05.050openalex-snapshot
A highly efficient microwave-assisted solvent-free synthesis of α- and β-2′-deoxy-1,2,3-triazolyl-nucleosides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.065openalex-snapshot
Ruthenium-catalyzed 1,3-dipolar cycloaddition of trifluoromethylated propargylic alcohols with azides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.07.101openalex-snapshot
Conjugation of an oligonucleotide to Tat, a cell-penetrating peptide, via click chemistry
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.077openalex-snapshot
Magnetically separable CuFe2O4 nano particles catalyzed multicomponent synthesis of 1,4-disubstituted 1,2,3-triazoles in tap water using ‘click chemistry’
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.128openalex-snapshot
One pot conjugation of small molecules to RNA using click chemistry
inferred← citeshttps://doi.org/10.1016/s0959-6380(05)80330-7openalex-snapshot
Five-membered ring systems: with more than one N atom
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.6b00221openalex-snapshot
Affinity Induced Surface Functionalization of Liposomes Using Cu-Free Click Chemistry
inferred← citeshttps://doi.org/10.1021/acs.biomac.5b00476openalex-snapshot
Functional Degradable Polymers by Radical Ring-Opening Copolymerization of MDO and Vinyl Bromobutanoate: Synthesis, Degradability and Post-Polymerization Modification
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01887openalex-snapshot
Relative Rates of Metal-Free Azide–Alkyne Cycloadditions: Tunability over 3 Orders of Magnitude
inferred← citeshttps://doi.org/10.1021/acs.langmuir.1c02390openalex-snapshot
Development of Highly Sensitive Molecular Blocks at Cancer Microenvironment for Rapid Cancer Cell Death
inferred← citeshttps://doi.org/10.1021/acs.macromol.6b00331openalex-snapshot
Synthesis of Functionalized Poly(lactic acid) Using 2-Bromo-3-hydroxypropionic Acid
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00055openalex-snapshot
Cationic 1,2,3-Triazolium Alkynes: Components To Enhance 1,4-Regioselective Azide–Alkyne Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1021/acscatal.0c00369openalex-snapshot
Metalloprotein-Catalyzed Click Reaction for In Situ Generation of a Potent Inhibitor
inferred← citeshttps://doi.org/10.1021/ar200059zopenalex-snapshot
Bioconjugation with Strained Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1021/ar200235mopenalex-snapshot
Click Dendrimers and Triazole-Related Aspects: Catalysts, Mechanism, Synthesis, and Functions. A Bridge between Dendritic Architectures and Nanomaterials
inferred← citeshttps://doi.org/10.1021/bc3005057openalex-snapshot
Quantitative Evaluation of Bioorthogonal Chemistries for Surface Functionalization of Nanoparticles
inferred← citeshttps://doi.org/10.1021/co3000117openalex-snapshot
Copper-free Route to Triazole-Modified Peptidomimetic by the Combination of Two Multicomponent Reactions in One Pot
inferred← citeshttps://doi.org/10.1021/cr0783479openalex-snapshot
Cu-Catalyzed Azide−Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1021/cr800448qopenalex-snapshot
Organic Synthesis “On Water”
inferred← citeshttps://doi.org/10.1021/ja043770+openalex-snapshot
Dynamic Ligand Exchange of the Lanthanide Complex Leading to Structural and Functional Transformation: One-Pot Sequential Catalytic Asymmetric Epoxidation-Regioselective Epoxide-Opening Process
inferred← citeshttps://doi.org/10.1021/ja409205sopenalex-snapshot
Fabrication of Highly Uniform Gel Coatings by the Conversion of Surface-Anchored Metal–Organic Frameworks
inferred← citeshttps://doi.org/10.1021/jo201434wopenalex-snapshot
Selective Transition State Stabilization via Hyperconjugative and Conjugative Assistance: Stereoelectronic Concept for Copper-Free Click Chemistry
inferred← citeshttps://doi.org/10.1021/jo5004086openalex-snapshot
1,n-Rearrangement of Allylic Alcohols Promoted by Hot Water: Application to the Synthesis of Navenone B, a Polyene Natural Product
inferred← citeshttps://doi.org/10.1021/jo502636dopenalex-snapshot
Intramolecular Etherification and Polyene Cyclization of π-Activated Alcohols Promoted by Hot Water
inferred← citeshttps://doi.org/10.1021/jo800676dopenalex-snapshot
Ionic Liquids/[bmim][N3] Mixtures: Promising Media for the Synthesis of Aryl Azides by SNAr
inferred← citeshttps://doi.org/10.1021/jo900594xopenalex-snapshot
Huisgen Cycloaddition Reaction of C-Alkynyl Ribosides under Micellar Catalysis: Synthesis of Ribavirin Analogues
inferred← citeshttps://doi.org/10.1021/jp077603iopenalex-snapshot
PVP-Stabilized Copper Nanoparticles: A Reusable Catalyst for “Click” Reaction between Terminal Alkynes and Azides in Nonaqueous Solvents
inferred← citeshttps://doi.org/10.1021/la200951xopenalex-snapshot
Surface Modification of Silicon Nanowires via Copper-Free Click Chemistry
inferred← citeshttps://doi.org/10.1021/la302880vopenalex-snapshot
Synthesis and Micropatterning of Photocatalytically Reactive Self-Assembled Monolayers Covalently Linked to Si(100) Surfaces via a Si–C Bond
inferred← citeshttps://doi.org/10.1021/ma202785xopenalex-snapshot
Generic, Metal-Free Cross-Linking and Modification of Silicone Elastomers Using Click Ligation
inferred← citeshttps://doi.org/10.1021/ma901447eopenalex-snapshot
Macromolecular Engineering through Click Chemistry and Other Efficient Transformations
inferred← citeshttps://doi.org/10.1021/ma902026jopenalex-snapshot
Polysiloxane Elastomers via Room Temperature, Metal-Free Click Chemistry
inferred← citeshttps://doi.org/10.1021/ol9002338openalex-snapshot
Benzyne Click Chemistry with in Situ Generated Aromatic Azides
inferred← citeshttps://doi.org/10.1039/9781839165375-00282openalex-snapshot
Engineered 3D Matrices with Spatiotemporally Tunable Properties
inferred← citeshttps://doi.org/10.1039/b812403eopenalex-snapshot
Copper-free ‘click’: 1,3-dipolar cycloaddition of azides and arynes
inferred← citeshttps://doi.org/10.1039/b821788bopenalex-snapshot
Versatile, efficient derivatization of polysiloxanes via click technology
inferred← citeshttps://doi.org/10.1039/c2ob26990bopenalex-snapshot
Chemoselective preparation of 1,2,3-triazole–isoxazole bisfunctional derivatives and their application in peptidomimetic synthesis
inferred← citeshttps://doi.org/10.1039/c3bm60159eopenalex-snapshot
In situ-forming robust chitosan-poly(ethylene glycol) hydrogels prepared by copper-free azide–alkyne click reaction for tissue engineering
inferred← citeshttps://doi.org/10.1039/c3cc47071gopenalex-snapshot
Biomimetic artificial ion channels based on beta-cyclodextrin
inferred← citeshttps://doi.org/10.1039/c3cs60386eopenalex-snapshot
Beyond click chemistry – supramolecular interactions of 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/c3ob41329bopenalex-snapshot
Bioorthogonal labelling of biomolecules: new functional handles and ligation methods
inferred← citeshttps://doi.org/10.1039/c6cs00907gopenalex-snapshot
Covalent post-assembly modification in metallosupramolecular chemistry
inferred← citeshttps://doi.org/10.1039/c9nj04690aopenalex-snapshot
The azide–alkyne cycloaddition catalysed by transition metal oxide nanoparticles
inferred← citeshttps://doi.org/10.1039/c9py00632jopenalex-snapshot
Benzyne–azide polycycloaddition: a facile route toward functional polybenzotriazoles
inferred← citeshttps://doi.org/10.1039/d4ob01752hopenalex-snapshot
Strain-promoted azide–alkyne cycloaddition enhanced by secondary interactions
inferred← citeshttps://doi.org/10.1039/d4ra01776eopenalex-snapshot
An easy and simple method for the immobilization of dyes through click reactions: activated alkyne, copper not needed
inferred← citeshttps://doi.org/10.1055/s-0042-1751452openalex-snapshot
Recent Advancements in Triazole-based Click Chemistry in Cancer Drug Discovery and Development
inferred← citeshttps://doi.org/10.1055/sos-sd-113-00177openalex-snapshot
13.13.6 1,2,3-Triazoles (Update 2015)
inferred← citeshttps://doi.org/10.1071/ch19670openalex-snapshot
An Expeditious Route for the Synthesis of Oxazepine Triazolo-β-Lactams through Intramolecular Metal-Free [3 + 2] Azide–Alkyne Cycloaddition
inferred← citeshttps://doi.org/10.1080/00397910601133599openalex-snapshot
Sonochemical Synthesis of 1,4‐Disubstituted 1,2,3‐Triazoles in Aqueous Medium
inferred← citeshttps://doi.org/10.1080/02678292.2012.733034openalex-snapshot
Copper-free click chemistry between azides and internal alkynes for triphenylene discotic liquid crystal trimer formation
inferred← citeshttps://doi.org/10.1134/s1068162010040011openalex-snapshot
Modification of nucleic acids using [3 + 2]-dipolar cycloaddition of azides and alkynes
inferred← citeshttps://doi.org/10.1134/s1070363220120300openalex-snapshot
Synthesis and Evaluation of Antioxidant, Antibacterial, and Target Protein-Molecular Docking of Novel 5-Phenyl-2,4-dihydro-3H-1,2,4-triazole Derivatives Hybridized with 1,2,3-Triazole via the Flexible SCH2-Bonding
inferred← citeshttps://doi.org/10.1134/s1070428012120196openalex-snapshot
Highly efficient synthesis of 4-trialkylsilyl(germyl)-1H-1,2,3-triazole-5-carbaldehydes
inferred← citeshttps://doi.org/10.1295/polymj.pj2008312openalex-snapshot
Synthesis and Characterization of a New Polytriazole Resin Derived from N,N-Dipropargyl-p-propargyloxyaniline
inferred← citeshttps://doi.org/10.1517/17460441.2012.682725openalex-snapshot
The impact of click chemistry in medicinal chemistry
inferred← citeshttps://doi.org/10.18297/etd/3718openalex-snapshot
Micellar nanocatalysis for efficient reactions.
inferred← citeshttps://doi.org/10.2174/1385272826666220126153429openalex-snapshot
Scientific and Technological Prospecting of 1H-1,2,3-Triazoles
inferred← citeshttps://doi.org/10.2174/1385272827666230201103825openalex-snapshot
Mechanisms, Copper Catalysts, and Ligands Involved in the Synthesis of 1,2,3- Triazoles Using Click Chemistry
inferred← citeshttps://doi.org/10.2174/1570179416666190704112904openalex-snapshot
A Novel Series of N-aryltriazole and N-acridinyltriazole Hybrids as Potential Anticancer Agents
inferred← citeshttps://doi.org/10.25103/jestr.134.10openalex-snapshot
Preparation and Characterization of Bis-Propargyl-Succinate, and its Application in Preliminary Healing Ability of Crosslinked Polyurethane using “Azide-Alkyne” Click
inferred← citeshttps://doi.org/10.25135/acg.oc.177.2412.3374openalex-snapshot
Synthesis, characterization, antioxidant, in silico-based virtual screening and anti-cancer potential of substituted 2-(4-acetyl-5-methyl-1h-1,2,3-triazol-1-yl)-n-phenylacetamide derivatives
inferred← citeshttps://doi.org/10.26686/wgtn.21377622openalex-snapshot
Studies on Proximity-Induced Cycloaddition for Bioconjugation
inferred← citeshttps://doi.org/10.3390/molecules16097980openalex-snapshot
Thymidine Analogues for Tracking DNA Synthesis
inferred← citeshttps://doi.org/10.3390/molecules21121697openalex-snapshot
Structural Determinants of Alkyne Reactivity in Copper-Catalyzed Azide-Alkyne Cycloadditions
inferred← citeshttps://doi.org/10.3390/polym10050516openalex-snapshot
Reactive Energetic Plasticizers Utilizing Cu-Free Azide-Alkyne 1,3-Dipolar Cycloaddition for In-Situ Preparation of Poly(THF-co-GAP)-Based Polyurethane Energetic Binders
inferred← citeshttps://doi.org/10.3987/rev-06-608openalex-snapshot
1,3-Dipolar Cycloadditions in Aqueous Media
inferred← citeshttps://doi.org/10.3987/rev-16-848openalex-snapshot
Dipolar Cycloadditions of Nitrones in Aqueous Media
inferred← citeshttps://doi.org/10.5012/bkcs.2005.26.11.1790openalex-snapshot
Facile Synthesis of Fréchet Type Dendritic Benzyl Azides and Dendrimer via Cycloaddition Reaction with Tripodal Core
inferred← citeshttps://doi.org/10.5772/28719openalex-snapshot
Protein Engineering with Non-Natural Amino Acids
inferred← citeshttps://doi.org/10.70675/4d78c293z7475z4fdaz9b89z44044f62a5dbopenalex-snapshot
Développement d'un microsystème séparatif sur monolithe organique pour l'analyse des radionucléides en milieu acide nitrique
inferred← citeshttps://doi.org/10.70675/86600575ze385z4365za25bzed713a6df420openalex-snapshot
Utilisation des liquides ioniques dans des réactions à économies d'atomes : l'addition de Michael et la cycloaddition 1,3-dipolaire
inferred← citeshttps://doi.org/10.70675/ad14db42z4c46z4a61z9990zed0277f671a9openalex-snapshot
Synthèse de matériaux moléculaires pour la conception de cellules solaires photoélectrocatalytiques
inferred← citeshttps://doi.org/10.70675/cb17791bz5024z452aza488zeb5e78a2849eopenalex-snapshot
Une nouvelle stratégie de synthèse de vaccins glycoconjugués
inferred← citeshttps://doi.org/10.70675/dc52adbbz4943z4109zb4bez68b5f0cca291openalex-snapshot
Design and synthesis of chemical tools and inhibitors for the study of L,D-transpeptidases involved in the peptidoglycan biosynthesis
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.