Results 101 to 110 of about 11,111 (220)

Modulating catalytic activity of polymer-based cuAAC "click" reactions

open access: yes, 2011
The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is used to synthesize complex polymer architectures. In this work, we demonstrate the control of this reaction at 25 degrees C between polystyrene (PSTY) chains through modulating the ...
Jia, Zhongfan   +7 more
core   +1 more source

Selective Chemical Modification of DNA with Boronic Acids by On-Column CuAAc Reactions

open access: yes, 2020
International audienceThe use of the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction for the preparation of oligonucleotide conjugates is by now familiar.
Debiais, Mégane   +3 more
core   +1 more source

A Portal‐Preorganized Cucurbit[7]uril‐Ruthenium Conjugate Enables Motif‐Selective Protein Sensing

open access: yesAngewandte Chemie International Edition, EarlyView.
Reprogramming cucurbit[7]uril (CB7) recognition through portal engineering transforms an optically silent host into a motif‐selective photoluminescent receptor. The portal‐preorganized CB7‐Rubpy conjugate directly reports changes in aromatic motif accessibility, enabling optical sensing of protein misfolding and refolding.
Patrick Gruhs   +10 more
wiley   +1 more source

Effects of a Flexible Alkyl Chain on a Ligand for CuAAC Reaction

open access: yes, 2016
Imidazole derivatives substituted by a normal alkyl group are shown to be efficient as a ligand for the copper(Ι)-catalyzed azide−alkyne cycloaddition (CuAAC) reaction. An alkyl chain on the imidazole ligands shows an efficient steric effect and benefits
Seijiro Matsubara (1490731)   +1 more
core   +1 more source

Safirinium Fluorescent “Click” Molecular Probes: Synthesis, CuAAC Reactions, and Microscopic Imaging

open access: yesMolecules
Fluorescent labeling utilizing Cu(I)-catalyzed azide–alkyne cycloaddition reactions (CuAAC) is among the leading applications of the “click” chemistry strategy.
Patryk Kasza   +10 more
doaj   +1 more source

Photopolymerization of Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) 'click'-based networks for new-age materials

open access: yes, 2018
Kloxin, Christopher J.The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is one of the most powerful tools in the ‘click’ chemistry toolbox and is immensely useful for an array of materials research avenues and applications.
Shete, Abhishek Umakant
core   +1 more source

Circular Photocaged mRNA for Light‐induced Late‐stage Activation of Translation

open access: yesAngewandte Chemie International Edition, EarlyView.
A clickable photo‐caged 5′ cap (CyCliCap) allows to make Cyclic Click Cap‐containing mRNA (CyCliCap‐mRNA) which is remarkably stable and translationally muted until irradiated, allowing for late‐stage activation of translation in cells by light. ABSTRACT mRNA is a new medical modality as vaccine and raises hopes to become a protein replacement agent ...
Bayram Terzi   +6 more
wiley   +1 more source

Quarternization of 3-azido-1-propyne oligomers obtained by copper(I)-catalyzed azide–alkyne cycloaddition polymerization

open access: yesBeilstein Journal of Organic Chemistry, 2015
3-Azido-1-propyne oligomer (oligoAP) samples, prepared by copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) polymerization, were quarternized quantitatively with methyl iodide in sulfolane at 60 °C to obtain soluble oligomers.
Shun Nakano   +2 more
doaj   +1 more source

Mitochondria‐endoplasmic reticulum organelle glue as maturation promoter for origination/dimensional dual‐cross cardiomyocytes

open access: yesBMEMat, EarlyView.
Mitochondria‐endoplasmic reticulum contact sites (MERCS) are areas where the mitochondria and endoplasmic reticulum closely interact. In this study, we utilize synthetic organelle glues to artificially engineer MERCS for regulating cardiomyocyte development, through which the immature and chemo‐plasticity issues of undifferentiated cells are addressed.
Wei Tang   +9 more
wiley   +1 more source

Site-Specific Modification of Proteins through N‑Terminal Azide Labeling and a Chelation-Assisted CuAAC Reaction

open access: yes, 2019
Site-specific modification of peptides and proteins is an important method for introducing an artificial function to the protein surface. Recently, we found that new bioconjugation reagents, 6-(azidomethyl)-2-pyridinecarbaldehyde (6AMPC) derivatives ...
Takashi Hayashi (298480)   +2 more
core   +1 more source

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