Results 21 to 30 of about 97,080 (283)

Apparent Copper(II)-Accelerated Azide−Alkyne Cycloaddition

open access: yes, 2016
Cu(II) salts accelerate azide−alkyne cycloaddition reactions in alcoholic solvents without reductants such as sodium ascorbate. Spectroscopic observations suggest that Cu(II) undergoes reduction to catalytic Cu(I) species via either alcohol oxidation or ...
Ronald J. Clark (547893)   +5 more
core   +4 more sources

Deposition of Ni(II)Porphyrin Monolayer on the Gold Electrode via Azide-Alkyne Click - Coupling and its Electrochemical Characterization

open access: yesInternational Journal of Electrochemical Science, 2014
In this work, a Ni(II)porphyrin containing two azide groups ((N3)2-Ni(II)porphyrin) was applied for gold electrode modification via azide-alkyne click reaction.
Iwona Grabowska   +7 more
doaj   +1 more source

Synthesis of Novel C-2- or C-15-Labeled BODIPY—Estrone Conjugates

open access: yesMolecules, 2018
Novel BODIPY–estrone conjugates were synthesized via Cu(I)-catalyzed azide–alkyne cycloaddition (CuAAC). Estrone-alkynes or an estrone-azide as starting compounds were synthesized via Michael addition or Sonogashira reaction as key steps ...
Ildikó Bacsa   +6 more
doaj   +1 more source

Toward Long-Term-Dispersible, Metal-Free Single-Chain Nanoparticles

open access: yesNanomaterials, 2023
We report herein on a new platform for synthesizing stable, inert, and dispersible metal-free single-chain nanoparticles (SCNPs) via intramolecular metal-traceless azide–alkyne click chemistry.
Agustín Blázquez-Martín   +5 more
doaj   +1 more source

Extending the scope of the C-functionalization of cyclam via Copper(I)-catalyzed Alkyne-Azide Cycloaddition to bifunctional chelators of interest

open access: yes, 2023
Cyclam, known for its potent chelation properties, is explored for diverse applications through selective N-functionalization, offering versatile ligands for catalysis, medical research, and materials science.
Raphael, Tripier   +5 more
core   +1 more source

Nitrogen-Based Linkers with a Mesitylene Core: Synthesis and Characterization

open access: yesMolecules, 2021
Mesitylene was used as a core in seven new tritopic nitrogen containing linkers. Three of the linkers, each containing three nitrile groups, were obtained through Suzuki, Sonogashira and Heck-type coupling reactions.
Lucian Gabriel Bahrin   +5 more
doaj   +1 more source

Luminescent Lariat Aza-Crown Ether

open access: yesMolbank, 2010
Lariat ethers are interesting recognition motifs in supramolecular chemistry. The synthesis of a luminescent lariat ether with triglycol chain by azide–alkyne (Huisgen) cycloaddition is presented.
Burkhard König   +2 more
doaj   +1 more source

Luminescent Lariat Aza-Crown Ether Carboxylic Acid

open access: yesMolbank, 2010
Lariat ethers are interesting recognition motifs in supramolecular chemistry. The synthesis of a luminescent lariat aza-crown ether with a carboxyl group appended by azide-alkyne (Huisgen) cycloaddition is presented.
Burkhard König   +2 more
doaj   +1 more source

A Genetically Encoded Picolyl Azide for Improved Live Cell Copper Click Labeling

open access: yesFrontiers in Chemistry, 2021
Bioorthogonal chemistry allows rapid and highly selective reactivity in biological environments. The copper-catalyzed azide–alkyne cycloaddition (CuAAC) is a classic bioorthogonal reaction routinely used to modify azides or alkynes that have been ...
Birthe Meineke   +9 more
doaj   +1 more source

Peptoids and polyamines going sweet: Modular synthesis of glycosylated peptoids and polyamines using click chemistry

open access: yesBeilstein Journal of Organic Chemistry, 2013
Sugar moieties are present in a wide range of bioactive molecules. Thus, having versatile and fast methods for the decoration of biomimetic molecules with sugars is of fundamental importance.
Daniel Fürniss   +6 more
doaj   +1 more source

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