Results 21 to 30 of about 3,191,477 (292)

Functionalization of Polysulfones by Click Chemistry

open access: yesMacromolecular Chemistry and Physics, 2010
AbstractFunctionalization of polysulfones by using “Click” chemistry is described for the example of a small fluorescent analyte propargylpyrene. First, PSUs were converted to azido‐functionalized polymers by successive chloromethylation and azidation. Propargylpyrene was prepared independently as a fluorescent click component.
Toiserkani, Hojjat   +3 more
openaire   +4 more sources

Recent Advances in Click Chemistry Applied to Dendrimer Synthesis

open access: yesMolecules, 2015
Dendrimers are monodisperse polymers grown in a fractal manner from a central point. They are poised to become the cornerstone of nanoscale devices in several fields, ranging from biomedicine to light-harvesting. Technical difficulties in obtaining these
Mathieu Arseneault   +2 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

Click Chemistry with Cyclopentadiene

open access: yesChemical Reviews, 2021
Cyclopentadiene is one of the most reactive dienes in normal electron-demand Diels-Alder reactions. The high reactivities and yields of cyclopentadiene cycloadditions make them ideal as click reactions. In this review, we discuss the history of the cyclopentadiene cycloaddition as well as applications of cyclopentadiene click reactions. Our emphasis is
Brian J. Levandowski, Ronald T. Raines
openaire   +4 more sources

Click to learn, learn to click: Undergraduate Synthetic Organic Chemistry experiments [PDF]

open access: yes, 2022
The optimization of an undergraduate experiment for Organic Chemistry students is described to explore the concept of click chemistry. The preparation of a terminal fluorescent alkyne and an organic azide is reported consisting of simple steps. These are
Francisco, Santoyo-Gonzalez   +3 more
core   +2 more sources

Redox-Click Chemistry for Disulfide Formation from Thiols [PDF]

open access: yes, 2023
The dynamic disulfide linkage plays a vital role in various biological processes as well as drugs and biomaterials. Oxidation of thiols is a widely utilized approach for disulfide synthesis; however, achieving both optimal reactivity and selectivity ...
Xiaohe, Zhang   +19 more
core   +2 more sources

Unfolding Potential of Click Chemistry in Bioconjugation: A Review [PDF]

open access: yes, 2023
The application of click chemistry, specifically Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) and Strain-Promoted Azide-Alkyne Cycloaddition (SPAAC), in bioconjugation has shown tremendous promise in various biomedical fields.
Fathima Shadin, P
core   +1 more source

Phosphorus(V) Fluoride Exchange (PFEx): Multidimensional Click Chemistry from Phosphorus(V) Connective Hubs [PDF]

open access: yes, 2022
We report catalytic Phosphorus Fluoride Exchange (PFEx) as the latest advance in connective click-reaction technology. Emulating Nature, PFEx reaches into the biological world and creates stable tetrahedral P(V)- connections through efficient phosphorus ...
Shoujun, Sun   +5 more
core   +2 more sources

Organotitanium Click Chemistry [PDF]

open access: yes, 2023
The click chemistry of titanium exemplified by the “green” [3+2] cycloaddition of the [Ti-N3] moiety with nitriles RCN to form a tetrazole ligand, is currently limited in scope, but the future of this open and wide field is bright, full of promising ...
Gregory, Arzoumanidis   +1 more
core   +1 more source

Click chemistry and drug delivery: A bird's-eye view

open access: yesActa Pharmaceutica Sinica B, 2023
Click chemistry has been proven to be very useful in drug delivery. Due to the availability of a large number of click reactions with a various characteristics, selection of appropriate chemistry for a given application is often not a trivial task.
Shameer M. Kondengadan   +5 more
doaj   +1 more source

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