Results 41 to 50 of about 358,569 (255)
N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts. [PDF]
By employing an N-heterocyclic carbene (NHC) catalyst, we developed a versatile catalytic system that enables deaminative cross-coupling reactions of aldehydes with redox-active pyridinium salts.
Kim I, Im H, Lee H, Hong S.
europepmc +2 more sources
On the photochemical reaction of pyridinium salts with nucleophiles [PDF]
AbstractDFT calculations on the photochemical reaction of 1-n–N-butylpyridinium salt in water with hydroxide anion is in agreement with a singlet state process where the S2 state at λ = 253 nm can be converted into a Dewar isomer (2-butyl-2-azabicyclo[2.2.0]hexa-2,5-dien-2-yl cation).
openaire +4 more sources
Passivating Lead Halide Perovskites Using Pyridinium Salts with Superhalogen Atoms
Passivating lead halide perovskites using pyridinium salts has attracted enormous attention, but the excellent surface passivation of the halide perovskites has not been achieved by using only a pyridinium salt until now.
Dongjie Zhu (8897999) +3 more
core +2 more sources
Catalytic Photochemical Enantioselective α-Alkylation with Pyridinium Salts
We have developed a chiral amine catalyzed enantioselective α-alkylation of aldehydes with amino acid derived pyridinium salts as alkylating reagents. The reaction proceeds in the presence of visible light (390 nm) and in the absence of a photocatalyst ...
Santhivardhana Reddy, Yetra +2 more
core +1 more source
Graphical AbstractA novel series of 3-phenyl-coumarin derivatives containing pyridinium salts was prepared, indicating significant inhibitory activity against AChE and BuChE as well as precious neuroprotective and anti-Aβ aggregation effects.
Elaheh Babaei +14 more
doaj +1 more source
Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl-Alkyl Cross-Couplings. [PDF]
A Negishi cross-coupling of alkyl pyridinium salts and alkylzinc halides has been developed. This is the first example of alkyl–alkyl bond formation via cross-coupling of an alkyl amine derivative with an unactivated alkyl group, and allows both primary ...
Plunkett S +3 more
europepmc +2 more sources
Synthetically versatile alkyl sulfinates can be prepared from readily available amines, using Katritzky pyridinium salt intermediates. In a catalyst-free procedure, primary, secondary, and benzylic alkyl radicals are generated by photoinduced or ...
Jonathan A. Andrews +4 more
semanticscholar +1 more source
Investigation of the Pyridinium Ylide—Alkyne Cycloaddition as a Fluorogenic Coupling Reaction
The cycloaddition of pyridinium ylides with alkynes was investigated under mild conditions. A series of 13 pyridinium salts was prepared by alkylation of 4-substituted pyridines.
Simon Bonte +4 more
doaj +1 more source
Catalytic reactions of pyridinium and iminium ions
Watson, Mary P.The dissertation focuses on transition metal catalysis of cationic species to make C-C bonds. ☐ Chapter 1 describes a nickel-catalyzed Suzuki-Miyaura cross-coupling of benzylic pyridinium salts. The pyridinium salts act as electrophiles in
Guan, Weiye
core +1 more source
4,4′,4″-(Benzene-1,3,5-triyltris(ethyne-2,1-diyl))tris(1-methylpyridin-1-ium) Iodide
Despite having been known for a long time, quaternary 4,4′-bipyridinium salts, or viologens, are still a highly inspiring class of compounds, thanks to their peculiar redox and charge transfer properties.
Lorenza Romagnoli +2 more
doaj +1 more source

