On the public citation graph
Click Imaging of Biochemical Processes in Living Systems
0 signed · 74 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known work and none has been retracted — and get a dated CiteStamped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(20010601)40:11<2004::aid-anie2004>3.0.co;2-5openalex-snapshot
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
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.19610941213openalex-snapshot
Zur Existenz niedergliedriger Cycloalkine, I
inferredcites →https://doi.org/10.1002/cbic.200300721openalex-snapshot
Chemical Strategies for Activity‐Based Proteomics
inferredcites →https://doi.org/10.1002/ejoc.200500483openalex-snapshot
CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
inferredcites →https://doi.org/10.1002/prac.18930480114openalex-snapshot
Ueber die Einwirkung von Diazobenzolimid auf Acetylendicarbonsäuremethylester
inferredcites →https://doi.org/10.1016/s1359-6446(03)02933-7openalex-snapshot
The growing impact of click chemistry on drug discovery
inferredcites →https://doi.org/10.1021/cb6003228openalex-snapshot
A Comparative Study of Bioorthogonal Reactions with Azides
inferredcites →https://doi.org/10.1021/ja021381eopenalex-snapshot
Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
inferredcites →https://doi.org/10.1021/ja027748xopenalex-snapshot
Investigating Cellular Metabolism of Synthetic Azidosugars with the Staudinger Ligation
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/ja044996fopenalex-snapshot
A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems
inferredcites →https://doi.org/10.1021/ja0471525openalex-snapshot
Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and Intermediates
inferredcites →https://doi.org/10.1021/ja047629copenalex-snapshot
Presentation and Detection of Azide Functionality in Bacterial Cell Surface Proteins
inferredcites →https://doi.org/10.1021/ja054643wopenalex-snapshot
Selective Dye-Labeling of Newly Synthesized Proteins in Bacterial Cells
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/10.1039/b507209nopenalex-snapshot
Advances in cycloaddition polymerizations
inferredcites →https://doi.org/10.1070/rc2005v074n04abeh000893openalex-snapshot
1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring
inferredcites →https://doi.org/10.1073/pnas.0707090104openalex-snapshot
Copper-free click chemistry for dynamic in vivo imaging
inferredcites →https://doi.org/10.1073/pnas.2335201100openalex-snapshot
A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation
inferredcites →https://doi.org/10.1126/science.287.5460.2007openalex-snapshot
Cell Surface Engineering by a Modified Staudinger Reaction
inferredcites →https://doi.org/10.1351/pac198961040613openalex-snapshot
Kinetics and reaction mechanisms: selected examples from the experience of forty years
inferredcites →https://doi.org/10.2174/1570178054038885openalex-snapshot
Highlights in Organic Chemistry Advances in 1,3-Dipolar Cycloaddition Reaction of Azides and Alkynes - A Prototype of “Click” Chemistry
inferredcites →https://doi.org/10.2174/157017906775473920openalex-snapshot
Cycloadditions as a Method for Oligonucleotide Conjugation
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.4782925openalex-extracted
Synthesis and Investigation of Photophysical Properties of Fluorescent Dyes Obtained by the Knoevenagel Condensation Reaction of Mono, Di or Tri Formyl Aromatic Aldehydes and Various Ch Acids
inferred← citeshttps://doi.org/10.1002/9783527631582.ch10openalex-snapshot
Copper‐Catalyzed Azide‐Alkyne Cycloaddition (CuAAC)
inferred← citeshttps://doi.org/10.1002/9783527633388.ch7openalex-snapshot
New Reactions of Copper Acetylides: Catalytic Dipolar Cycloadditions and Beyond
inferred← citeshttps://doi.org/10.1002/9783527664801.ch7openalex-snapshot
CuAAC: The Quintessential Click Reaction
inferred← citeshttps://doi.org/10.1002/adsc.201000417openalex-snapshot
Nonafluorobutanesulfonyl Azide: A Shelf‐Stable Diazo Transfer Reagent for the Synthesis of Azides from Primary Amines
inferred← citeshttps://doi.org/10.1002/ange.200805507openalex-snapshot
Selektive Fluoreszenzmarkierung von Lipiden in lebenden Zellen
inferred← citeshttps://doi.org/10.1002/ange.200900942openalex-snapshot
Bioorthogonale Chemie – oder: in einem Meer aus Funktionalität nach Selektivität fischen
inferred← citeshttps://doi.org/10.1002/ange.201916352openalex-snapshot
Pre‐targeted Imaging of Protease Activity through In Situ Assembly of Nanoparticles
inferred← citeshttps://doi.org/10.1002/anie.200805507openalex-snapshot
Selective Fluorescence Labeling of Lipids in Living Cells
inferred← citeshttps://doi.org/10.1002/anie.200900942openalex-snapshot
Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
inferred← citeshttps://doi.org/10.1002/anie.201916352openalex-snapshot
Pre‐targeted Imaging of Protease Activity through In Situ Assembly of Nanoparticles
inferred← citeshttps://doi.org/10.1002/aoc.5156openalex-snapshot
Water as a solvent for Ru‐catalyzed click reaction: Highly efficient recyclable catalytic system for triazolocoumarins synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.200800699openalex-snapshot
An Overview of Syntheses of Apogalanthamine Analogues and 7‐Aza Derivatives of Steganacin and Steganone
inferred← citeshttps://doi.org/10.1002/ejoc.201000132openalex-snapshot
Synthesis of Hyperbranched β‐Galceramide‐Containing Dendritic Polymers that Bind HIV‐1 rgp120
inferred← citeshttps://doi.org/10.1002/ejoc.201101823openalex-snapshot
Nitrile Oxide/Alkyne Cycloadditions – A Credible Platform for Synthesis of Bioinspired Molecules by Metal‐Free Molecular Clicking
inferred← citeshttps://doi.org/10.1007/s12154-010-0047-1openalex-snapshot
In-cell click labelling of small molecules to determine subcellular localisation
inferred← citeshttps://doi.org/10.1007/s41061-015-0001-3openalex-snapshot
Transition-Metal-Catalyzed Bioorthogonal Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1016/bs.aihch.2019.10.005openalex-snapshot
Application of organic azides in the synthesis of heterocyclic systems
inferred← citeshttps://doi.org/10.1016/j.bbalip.2014.01.003openalex-snapshot
Fat & fabulous: Bifunctional lipids in the spotlight
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.004openalex-snapshot
In vivo click reaction between Tc-99m-labeled azadibenzocyclooctyne-MAMA and 2-nitroimidazole-azide for tumor hypoxia targeting
inferred← citeshttps://doi.org/10.1016/j.jmr.2010.03.019openalex-snapshot
Distance measurements in model bis-Gd(III) complexes with flexible “bridge”. Emulation of biological molecules having flexible structure with Gd(III) labels attached
inferred← citeshttps://doi.org/10.1016/j.jmr.2011.02.010openalex-snapshot
Pulsed dipolar spectroscopy distance measurements in biomacromolecules labeled with Gd(III) markers
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.10.005openalex-snapshot
Copper catalyzed synthesis of 1-aryl-1,2,3-triazoles from aryl iodides, alkynes, and sodium azide
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134325openalex-snapshot
Synthesis and investigation of photo-physical properties of fluorescent dyes obtained by the Knoevenagel condensation of mono-, di- or tri-formyl aromatic aldehydes and various CH-acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.114openalex-snapshot
Nano-copper catalyzed three-component reaction to construct 1,4-substituted 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c01108openalex-snapshot
A Not-So-Ancient Grease History: Click Chemistry and Protein Lipid Modifications
inferred← citeshttps://doi.org/10.1021/acs.organomet.8b00565openalex-snapshot
Mechanistic Study in Click Reactions by Using (N-Heterocyclic carbene)Copper(I) Complexes: Anionic Effects
inferred← citeshttps://doi.org/10.1021/bc800417bopenalex-snapshot
Monofunctional Carbocyanine Dyes for Bio- and Bioorthogonal Conjugation
inferred← citeshttps://doi.org/10.1021/bi200585nopenalex-snapshot
DNA-Catalyzed Covalent Modification of Amino Acid Side Chains in Tethered and Free Peptide Substrates
inferred← citeshttps://doi.org/10.1021/cr8004668openalex-snapshot
Selective Covalent Protein Immobilization: Strategies and Applications
inferred← citeshttps://doi.org/10.1021/jm901178dopenalex-snapshot
Synthesis and Antiprotozoal Activity of Cationic 1,4-Diphenyl-1H-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1021/jo3008572openalex-snapshot
RuH2(CO)(PPh3)3Catalyzed Selective Formation of 1,4-Disubstituted Triazoles from Cycloaddition of Alkynes and Organic Azides
inferred← citeshttps://doi.org/10.1021/mp100089kopenalex-snapshot
Uptake, Distribution and Diffusivity of Reactive Fluorophores in Cells: Implications toward Target Identification
inferred← citeshttps://doi.org/10.1021/om300513wopenalex-snapshot
Selective Formation of 1,4-Disubstituted Triazoles from Ruthenium-Catalyzed Cycloaddition of Terminal Alkynes and Organic Azides: Scope and Reaction Mechanism
inferred← citeshttps://doi.org/10.1021/om9005774openalex-snapshot
Copper-Catalyzed Huisgen [3 + 2] Cycloaddition of Gold(I) Alkynyls with Benzyl Azide. Syntheses, Structures, and Optical Properties
inferred← citeshttps://doi.org/10.1039/b904091aopenalex-snapshot
Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(i) acetylides
inferred← citeshttps://doi.org/10.1039/b904185kopenalex-snapshot
Fast, copper-free click chemistry: a convenient solid-phase approach to oligonucleotide conjugation
inferred← citeshttps://doi.org/10.1039/c3md00277bopenalex-snapshot
Target validation using in-cell small molecule clickable imaging probes
inferred← citeshttps://doi.org/10.1039/c3nj00468fopenalex-snapshot
Porous copper catalyzed click reaction in water
inferred← citeshttps://doi.org/10.1039/c5ra02703aopenalex-snapshot
Mechanism and selectivity for zinc-mediated cycloaddition of azides with alkynes: a computational study
inferred← citeshttps://doi.org/10.1039/c6cp04950hopenalex-snapshot
Towards understanding the kinetic behaviour and limitations in photo-induced copper( i ) catalyzed azide–alkyne cycloaddition (CuAAC) reactions
inferred← citeshttps://doi.org/10.1039/d0ra06251kopenalex-snapshot
Design and synthesis of magnetic Fe 3 O 4 @NFC-ImSalophCu nanocatalyst based on cellulose nanofibers as a new and highly efficient, reusable, stable and green catalyst for the synthesis of 1,2,3-triazoles
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/s1070428012040203openalex-snapshot
1,3-dipolar cycloaddition reactions in the series of N-alkynyl-substituted uracils
inferred← citeshttps://doi.org/10.1134/s1070428016100328openalex-snapshot
Copper(II) oxide nanowhiskers—A new efficient catalyst of azide–alkyne cycloaddition
inferred← citeshttps://doi.org/10.1371/journal.pone.0089899openalex-snapshot
Attenuation of Hedgehog Acyltransferase-Catalyzed Sonic Hedgehog Palmitoylation Causes Reduced Signaling, Proliferation and Invasiveness of Human Carcinoma Cells
inferred← citeshttps://doi.org/10.3762/bjoc.12.151openalex-snapshot
Dinuclear thiazolylidene copper complex as highly active catalyst for azid–alkyne cycloadditions
inferred← citeshttps://doi.org/10.3762/bjoc.9.308openalex-snapshot
Advancements in the mechanistic understanding of the copper-catalyzed azide–alkyne cycloaddition
inferred← citeshttps://doi.org/10.70675/2694eb23z3120z4665za3e9z32d07c922458openalex-snapshot
Synthèse et activité antimicrobienne d’assemblages moléculaires basés sur les dendrimères greffés de lysine
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.