Results 131 to 140 of about 9,152 (195)

<i>Ortho</i>-Methylation of pyridine <i>via</i> intramolecular <i>N</i>-methyl migration. [PDF]

open access: yesChem Sci
Huang SY   +10 more
europepmc   +1 more source

Heterogeneous photocatalytic C4 remote fluorosulfonamidation of pyridines. [PDF]

open access: yesChem Sci
Xiang P   +7 more
europepmc   +1 more source

HFIP-Induced Formation of <i>O</i>-Aryl Oxyallyl Cation and Nucleophilic Addition with Sodium Sulfinate Salt. [PDF]

open access: yesJ Org Chem
Aldás-Bedón J   +6 more
europepmc   +1 more source

Syntheses Using Pyridinium Salts

Angewandte Chemie International Edition in English, 1963
AbstractThis review discusses syntheses leading to a new type of N‐vinylpyridinium salts, to novel anionocyanines, to aminophenazines and alloxazines, as well as to (aza‐) dehydroquinolizinium, acridizinium, and morphanthridizinium salts. In addition, Mannich reactions and aminoalkylations at active methylene groups of cycloimmonium salts, and their ...
exaly   +2 more sources

The synthetic potential of pyridinium salt photochemistry

Photochemical & Photobiological Sciences, 2008
The discovery in the 1970s by Kaplan, Wilzbach and Pavlik that pyridinium salts undergo a unique cyclization reaction to produce bicyclic-aziridines was virtually unrecognized for nearly three decades. It was only comparatively recently that the process was explored in more detail and its synthetic potential exploited.
Jiwen, Zou, Patrick S, Mariano
openaire   +2 more sources

Infrared spectra of pyridinium salts in solution—III. Associations of pyridinium salts with bases

Spectrochimica Acta Part A: Molecular Spectroscopy, 1983
Associations of pyridinium salts X-Py+HA− (A− = SbCl−6, ClO−4, BF−4, I−, Br− and Cl−) with a wide series of aprotic bases and with protic solvents (water and fluoroalcohols) have been studied by infrared spectroscopic methods. Constants of association Ka of the pyridinium salts with the bases at different temperatures have been measured and enthalpy ...
S.E. Odinokov   +2 more
openaire   +1 more source

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