Results 1 to 10 of about 11,349 (193)

Peptide Conjugation via CuAAC ‘Click’ Chemistry

open access: yesMolecules, 2013
The copper (I)-catalyzed alkyne azide 1,3-dipolar cycloaddition (CuAAC) or ‘click’ reaction, is a highly versatile reaction that can be performed under a variety of reaction conditions including various solvents, a wide pH and temperature range, and ...
Mariusz Skwarczynski   +2 more
exaly   +4 more sources

Development and Applications of the Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) as a Bioorthogonal Reaction

open access: yesMolecules, 2016
The emergence of bioorthogonal reactions has greatly broadened the scope of biomolecule labeling and detecting. Of all the bioorthogonal reactions that have been developed, the copper-catalyzed azide-alkyne cycloaddition (CuAAC) is the most widely ...
Zhiyuan Zhang
exaly   +4 more sources

1,2,3-Triazole-linked DNA biosensors: molecular design to real-time applications [PDF]

open access: yesRSC Advances
Many aspects of modern life rely on rapid, accurate, and selective detection methodologies, especially for heavy toxins, pathogens, biomolecules, metal ions, and miRNAs.
Gaurav Bhatoe   +4 more
doaj   +2 more sources

Advancements and applications of click chemistry in protein labeling and bioconjugation [PDF]

open access: yesRSC Advances
Click chemistry has emerged as a versatile and efficient chemical strategy for constructing complex molecules under mild conditions. Its core reaction is copper(i)-catalyzed azide–alkyne cycloaddition (CuAAC), which provides high yields ...
Usman Nazeer, Guoting Qin, Chengzhi Cai
doaj   +2 more sources

A SPAAC-Based Bioorthogonal Method for Verifying Protein Palmitoylation [PDF]

open access: yesBio-Protocol
Palmitoylation is a crucial post-translational modification, and bioorthogonal chemistry based on azide-alkyne cycloaddition is typically used to verify protein palmitoylation.
Yaoyu Zhang   +6 more
doaj   +2 more sources

Pathway selection between click and acyl transfer reactions driven by aminoacyl phosphates [PDF]

open access: yesNature Communications
Covalent transformations in biology follow defined temporal sequences that regulate processes such as acylation and phosphorylation, yet achieving comparable temporal control in synthetic systems remains challenging.
Debjyoti Bhattacharjee   +6 more
doaj   +2 more sources

Catalytic Enantioselective Construction of Planar Chiral Heterocyclic [2.2]Paracyclophanes Enabled by Copper-Catalyzed Desymmetric Azide-Alkyne Cycloaddition [PDF]

open access: yesNature Communications
The construction of planar chiral [2.2]paracyclophanes (PCPs) is of great importance due to their intriguing photophysical and optoelectronic properties.
Zhuang-Zhuang Li   +2 more
doaj   +2 more sources

Atroposelective interrupted CuAAC reaction using cyclic diaryliodoniums [PDF]

open access: yesNature Communications
Copper-catalyzed azide–alkyne cycloaddition (CuAAC) is a pivotal strategy for joining two fragments, including bioactive moieties under mild conditions.
Yuanyuan Li   +3 more
doaj   +2 more sources

Novel CuCLIP-seq for in situ covalently captured protein-binding RNAs [PDF]

open access: yesNature Communications
RNA binding proteins (RBPs) are multi-faceted proteins that interact with transcripts in various RNA driven processes and functions. However, in situ covalent capture techniques for screening authentic RNA substrates of RBPs remain challenging in terms ...
Xing Wang   +11 more
doaj   +2 more sources

Click chemistry as a promising protocol for fluorogenic reactions [PDF]

open access: yesRecords of Pharmaceutical & Biomedical Sciences, 2023
The Nobel prize in chemistry has been awarded to the click chemistry approach in 2022 due to its significant impact on nearly all fields of chemical science.
Heba Aref   +4 more
doaj   +1 more source

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