Results 151 to 160 of about 9,595 (203)

Dimerization of pyridinium salts by cyanide

Journal of the Chemical Society D: Chemical Communications, 1970
1,1′-Dihydro-4,4′-bipyridyls (II) are formed from certain pyridinium or 2-methylpyridinium salts and sodium cyanide.
Lawrence J. Winters, Nelson G. Smith, Martin I. Cohen   +2 more
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N-(?-ferrocenylalkyl) pyridinium salts

Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 1966
1. N- (α-Ferrocenylalkyl)pyridinium p-toluenesulfonates are formed when ferrocenylcarbinols are reacted with p-toluenesulfonyl chloride in pyridine. 2. The N-(α-ferrocenylalkyl)pyridinium salts are good ferrocenylalkylating agents.
A. N. Nesmeyanov, E. G. Perevalova, M. D. Reshetova   +2 more
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Imidazo [1,2‐a] pyridinium salts

Journal of Heterocyclic Chemistry, 1965
Abstract2‐Alkylamino‐ or arylaminopyridines react directly with α‐bromoketones to afford 1‐alkyl‐ or 1‐arylimidazo[1,2‐a]pyridinium salts with substituents at position 2. Use of chloroacetaldoxime as the quaternizing agent yields (after hydrolysis) the imidazo‐[1,2‐a]pyridinium ion with no substituent at position 2.
C. K. Bradsher, E. F. Litzinger, M. F. Zinn   +2 more
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Pyridinium Salts as Organophosphate Antagonists

2015
By a standard screening in vivo, a series of pyridinium salts were tested for their protective activity against organophosphate poisoning. In order to obtain information about the protective mechanisms, several biochemical properties of these compounds were investigated in vitro, viz., their influence upon the enzymes cholineacetyltransferase and ...
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Thiazolo [3,2‐a] pyridinium salts

Journal of Heterocyclic Chemistry, 1966
AbstractThe sulfides formed by the reaction of α‐halo ketones or α‐halo acetals with 2‐mercaptopyridine may be cyclized in good yield to form thiazolo[3, 2‐a]pyridinium salts. The presence of chloro or nitro substituents on the pyridine ring does not interfere with the synthesis.
C. K. Bradsher, D. F. Lohr
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The reaction of N-nitrosamines with pyridinium salts

Talanta, 1988
N-Nitrosamines react readily with pyridinium salts containing an activated methylene group to give hydrazones. This reaction may serve as the basis for the routine determination of N-nitrosamines.
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Catalytic hydrogenation of pyridinium salts

Chemistry of Heterocyclic Compounds, 1994
Catalytic hydrogenation of polysubstituted pyridinium salts leads to piperidines and their condensed analogs The spatial properties and conformational properties of the saturated azaheterocycles have been determined by13C NMR spectorscopy. It was shown that hydrogenation of the pyridinium salts occurs stereoselectively to form cis isomers in most cases.
P. V. Reshetov, S. A. Rozhnova, A. P. Kriven'ko   +2 more
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VIBRATIONAL SPECTRA OF PYRIDINIUM SALTS

Canadian Journal of Chemistry, 1961
The vibrational spectrum of the pyridinium ion, C5H5NH+, and the N-deuterated species has been studied in several pyridinium salts. By comparison with benzene and deuterobenzene (with which the pyridinium ion is isoelectronic) a fairly complete assignment has been made. The N—H bonds, which are hydrogen bonded to the anions, have stretching vibrations
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Synthesis and characterizations of pyridinium salts including poly(pyridinium salt)s and their applications

2012
Pyridinium salts, both molecular and polymeric, are an interesting class of multifunctional materials that exhibit liquid-crystalline and light-emitting properties. Moreover, their properties can be easily tuned by introducing new types of anions or by modifying their chemical structures.
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Oxidation of polysubstituted pyridinium salts

Collection of Czechoslovak Chemical Communications, 1982
Oxidation of 1-substituted 2,4,6-triphenylpyridinium salts Ia-Ij with potassium ferricyanide in an alkaline medium was accompanied by contraction of the pyridine ring and formation of 1,2,3,5-tetrasubstituted pyrroles II. The derivative IIf underwent facile electrophilic substitution in the position 4. Contrary to compounds Ia-Ij, the 1-substituted-2,6-
Petr Nesvadba, Josef Kuthan
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