Results 1 to 10 of about 4,940,768 (329)

Photo Click Reaction of Acylsilanes with Indoles. [PDF]

open access: yesAngew Chem Int Ed Engl, 2021
Light‐mediated coupling of acylsilanes with indoles is reported. This photo click reaction occurs under mild conditions (415 nm) mostly in quantitative yield and provides stable silylated N,O‐acetals via light mediated siloxycarbene generation with ...
Stuckhardt C, Wissing M, Studer A.
europepmc   +6 more sources

Salt Metathesis: An Ultimate Click Reaction [PDF]

open access: yesPrecision Chemistry
In this Comment, we suggest salt metathesis (or ion exchange) as an ultimate click reaction, extending click chemistry principles beyond covalent bonds to ionic interactions. These universal and robust reactions, which nature utilizes in marine organisms' biomineralization processes, proceed spontaneously under mild conditions with minimal waste ...
Christopher M. Butch   +2 more
doaj   +4 more sources

Design of mechanical-robust phosphorescence materials through covalent click reaction. [PDF]

open access: yesNat Commun, 2023
It remains a great challenge to engineer materials with strong and stable interactions for the simultaneously mechanical-robust and room temperature phosphorescence-efficient materials.
Tian R, Gao S, Li K, Lu C.
europepmc   +2 more sources

Overview of 1,5-Selective Click Reaction of Azides with Alkynes or Their Synthetic Equivalents [PDF]

open access: yesMolecules, 2023
Nowadays, the click reaction of azides with alkynes has evolved rapidly and become one of the most efficient methods to synthesize 1,2,3-triazoles, which are an important class of N-containing heterocycles.
Yaqi Zhao   +3 more
doaj   +2 more sources

Copper(I)-Catalyzed Alkyne-Azide Cycloaddition (CuAAC) "Click" Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms. [PDF]

open access: yesACS Omega, 2023
Click chemistry is currently one of the most used tools for the generation of complex organic molecules. The advantages of using click chemistry in organic synthesis are remarkable; in many cases, the reactions occur under mild conditions and are free of
Pineda-Castañeda HM   +2 more
europepmc   +2 more sources

Conformation of G-quadruplex Controlled by Click Reaction [PDF]

open access: yesMolecules, 2020
G-quadruplexes are non-canonical four stranded secondary structures possessing great biological importance. Controlling G-quadruplex conformation for further regulating biological processes is both exciting and challenging.
Chao-Da Xiao   +4 more
doaj   +3 more sources

Post-Functionalization of Organometallic Complexes via Click-Reaction [PDF]

open access: yesMolecules, 2022
CuAAC (Cu catalyzed azide-alkyne cycloaddition) click-reaction is a simple and powerful method for the post-synthetic modification of organometallic complexes of transition metals. This approach allows the selective introduction of additional donor sites
Stanislav Petrovskii   +4 more
doaj   +2 more sources

An Inorganic Click Reaction for the Synthesis of Interlocked Molecules. [PDF]

open access: yesAngew Chem Int Ed Engl, 2023
AbstractWe describe the use of the cyaphide‐azide 1,3‐dipolar cycloaddition reaction for the synthesis of a new class of inorganic rotaxanes containing gold(I) triazaphosphole stoppers. Electron‐deficient bis‐azides, which thread perethylated pillar[5]arene in aromatic solvents, readily react with two equivalents of Au(IDipp)(CP) (IDipp=1,3‐bis‐(2,6 ...
Mapp A   +3 more
europepmc   +3 more sources

Electrostatic catalysis of a click reaction in a microfluidic cell. [PDF]

open access: yesNat Commun
AbstractElectric fields have been highlighted as a smart reagent in nature’s enzymatic machinery, as they can directly trigger or accelerate chemical processes with stereo- and regio-specificity. In enzymatic catalysis, controlled mass transport of chemical species is also key in facilitating the availability of reactants in the active reaction site ...
Sevim S   +11 more
europepmc   +6 more sources

Superstructures of fluorescent cyclodextrin via click-reaction [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2013
Mono-(6-azido-6-deoxy)-β-cyclodextrin (CD) was covalently attached to an alkyne-modified 5-methyl-2-(pyridin-2-yl)thiazol-4-ol yielding a fluorophore containing CD in a click-type reaction.
Arkadius Maciollek   +2 more
doaj   +4 more sources

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