Results 211 to 220 of about 15,690 (247)
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Simultaneous Photoinduced ATRP and CuAAC Reactions for the Synthesis of Block Copolymers
Macromolecular Rapid Communications, 2014Atom transfer radical polymerization (ATRP) and copper‐catalyzed azide–alkyne cycloaddition (CuAAC) reactions, both utilizing copper(I) (Cu(I)) complexes, make a tremendous progress in synthetic polymer chemistry. Independently or in combination with other polymerization processes, they give access to the synthesis of polymers with well‐defined ...
Yusuf Yagci
exaly +3 more sources
Biocompatible photoinduced CuAAC using sodium pyruvate
Chemical Communications, 2021The use of sodium pyruvate as a photoreducing agent for copper-mediated azide–alkyne cycloaddition (CuAAC) under UV irradiation is described.
Jaepil Jeong +7 more
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Copper-Mediated Intramolecular Interrupted CuAAC Selanylation
The Journal of Organic Chemistry, 2023We, herein, describe a copper-mediated domino CuAAC intramolecular selanylation for the synthesis of unprecedented fused benzo[4,5][1,3]selenazolo[3,2-c][1,2,3]triazoles from 1,2-bis(2-azidoaryl)diselenides and terminal alkynes under microwave irradiation.
Wystan K. O. Teixeira +5 more
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2022
AbstractThe basic principles of the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), widely considered to be the first click reaction, are described. This involves amongst others the concept of click reactions, the mechanism of CuAAC, the synthesis and reactivity of organic azides and acetylenes, an overview of most commonly used copper(I)
F. F. Ort, F. P. J. T. Rutjes
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AbstractThe basic principles of the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), widely considered to be the first click reaction, are described. This involves amongst others the concept of click reactions, the mechanism of CuAAC, the synthesis and reactivity of organic azides and acetylenes, an overview of most commonly used copper(I)
F. F. Ort, F. P. J. T. Rutjes
openaire +1 more source
2.4 CuAAC in Carbohydrate Conjugation
2022AbstractCopper(I)-catalyzed azide–alkyne cycloaddition reactions (CuAAC), as a versatile, reliable, and modular strategy, have been widely investigated in the area of glycoscience during the last 20 years. Herein, we presented a brief overview of CuAAC click approaches for easy access to diverse simple and complex triazole-appended carbohydrate ...
A. K. Agrahari, A. Mishra, V. K. Tiwari
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2.3 CuAAC in Protein Conjugation
2022AbstractThis chapter summarizes the use of the copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction in the synthesis of peptide and protein conjugates. The different reaction conditions used for construction of the conjugates and their application in various disciplines are covered. Synthetic strategies for the introduction of the click groups (
A. La Venia, A. Kovalová, M. Vrabel
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2.2 CuAAC in Peptidomimetics and Protein Mimics
2022AbstractThe tremendous recent developments in click chemistry, including the impressive developments of strain-promoted cycloaddition reagents, all started with the copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction conceived by Meldal et al. and Sharpless et al.
T. J. Meuleman, R. M. J. Liskamp
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2021
Fil: Kovalova, Ana. Czech Academy of Sciences.
la Venia, Agustina +2 more
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Fil: Kovalova, Ana. Czech Academy of Sciences.
la Venia, Agustina +2 more
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The application of CuAAC ‘click’ chemistry to catenane and rotaxane synthesis
Chem. Soc. Rev., 2010The copper(I)-catalysed azide-alkyne cycloaddition (the CuAAC 'click' reaction) is proving to be a powerful new tool for the construction of mechanically interlocked molecular-level architectures. The reaction is highly selective for the functional groups involved (terminal alkynes and azides) and the experimental conditions are mild and compatible ...
Leigh, D A; id_orcid 0000-0002-1202-4507 +1 more
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Arylazopyrazoles for Conjugation by CuAAC Click Chemistry
The Journal of Organic ChemistryMolecular photoswitches are increasingly being implemented in bioactive compounds and responsive materials. For this purpose, photoswitches must be coupled to a wide variety of substrates and scaffolds. We present a library of "clickable" arylazopyrazoles (AAPs), which can be conjugated by Cu-catalyzed alkyne azide cycloaddition (CuAAC).
Alisa-Maite Kauth +2 more
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