Results 31 to 40 of about 47,136 (264)
2-(Benzenesulfonamido)pyridinium nitrate [PDF]
In the title compound, C11H11N2O2S+·NO3−, the dihedral angle between the benzene and pyridinium rings is 87.59 (8)°. An intramolecular C—H...O interaction occurs in the cation. In the crystal structure, ion pairs occur, being linked by two strong N—H...O interactions, formingR22(8) loops. The packing is further stabilized by weak C—H...O interactions.
Jiang-Sheng Li, Xun Li
openaire +3 more sources
Pyridinium-2-carboxylate–benzene-1,2-diol (1/1)
The title compound, C6H5NO2·C6H6O2, crystallizes with one pyridinium-2-carboxylate zwitterion and one molecule of benzene-1,2-diol in the asymmetric unit.
Bolte, Michael +3 more
core +1 more source
2-(Benzenesulfonamido)pyridinium perchlorate [PDF]
In the title compound, C11H11N2O2S+·ClO4−, the dihedral angle between the benzene and pyridinium rings is 87.33 (10)°. An intramolecular N—H...O interaction, with an S=O-bonded O atom as receptor, occurs in the cation. In the crystal structure, ion pairs occur, being linked by strong N—H...O hydrogen bonds. The perchlorate anion plays a further role in
Xun Li +3 more
openaire +3 more sources
4-[3-(Isonicotino-yloxy)propoxycarbon-yl]pyridinium diiodidoargentate(I)
The structure of the title compound, (C15H15N2O4)[AgI2], consists of an organic 4-[3-(isonicotinoyloxy)propoxycarbonyl]pyridinium cation which has a gauche–gauche (O/C/C/C—O/C/C/C or GG’) conformation and lies on a twofold rotation axis, which passes ...
Bolte, Michael +12 more
core +1 more source
Cell surface proteins (CSPs) are valuable targets for therapeutic agents, but achieving highly selective CSP enrichment in cellular physiology remains a technical challenge.
Yongli Li (527489) +13 more
core +3 more sources
Mechanochemistry Meets Catalysis: Metal Complexes for Greener Organic Transformations
Mechanochemistry is redefining metal catalysis by controlling catalyst formulation, speciation, and deployment. This Review shows how milling, LAG, RAM, and TSE enable rapid metal‐complex assembly, distinctive catalytic manifolds, and scalable synthesis beyond solution chemistry.
Sourav Behera +2 more
wiley +2 more sources
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
Regioselective Alkylation of Pyridinium Riboses [PDF]
The nucleophilic addition of alkyl, benzyl, and allyl organozinc reagents to protected pyridinium riboses proceeds under mild conditions and with yields of > 90 % in several cases and complete regioselectivity for the 4‐position.
Farbod Salahi, Olaf Wiest
openaire +2 more sources
Mitochondria‐Targeting Moieties Based on N‐Tethered Pyridinium Cations
Pyridinium cations were benchmarked as mitochondria‐targeting moieties in a panel of N‐tethered fluorescent‐, bioactive‐, and inert‐cargo conjugates. 3,5‐Diphenylpyridinium (DPPy+) is a competent triphenylphosphonium (TPP+) surrogate, combining high mitochondria‐targeting efficiency with lower intrinsic effects on mitochondrial function.
Ivan Džajić +27 more
wiley +2 more sources
A library of N-benzylpyridinium-based compounds, 7a-j and 8a-j, was designed and synthesised as potential acetylcholinesterase) AChE (inhibitors. An in vitro assay for the synthesised compounds showed that most compounds had significant AChE inhibitory ...
Nafisah M. Al-Rifai +4 more
doaj +1 more source

