19424-15-8Relevant articles and documents
Dithionite adducts of pyridinium salts: Regioselectivity of formation and mechanisms of decomposition
Carelli, Vincenzo,Liberatore, Felice,Scipione, Luigi,Di Rienzo, Barbara,Tortorella, Silvano
, p. 10331 - 10337 (2007/10/03)
1H and 13C NMR spectroscopy has been used to detect and to characterize the adducts formed, in alkaline solutions, by the attack of dithionite anion on 3-carbamoyl or 3-cyano substituted pyridinium salts. In all studied cases, only 1,4-dihydropyridine-4-sulfinates, formed by attack of dithionite oxyanion on the carbon 4 of pyridinium ring, were found. This absolute regioselectivity seems to suggest a very specific interaction between the pyridinium cation and the dithionite through the formation of a rigidly oriented ion pair, determining the position of attack. In weak alkaline solution, the adducts decompose according to two mechanisms SNi and SNi′: the SNi path is operative in all studied cases and preserves the 1,4-dihydro structure yielding the corresponding 1,4-dihydropyridines, whereas the SNi′ path involves the shift of 2,3 or 5,6 double bonds yielding 1,2- or 1,6-dihydropyridines, respectively. The formation of 1,2- or 1,6-dihydropyridines, in addition to 1,4-dihydro isomers, depends on their respective thermodynamic stabilities.
Kinetics of the reduction of nicotinonitrile cations by 1,4-dihydronicotinamides
Bunting, John W.,Brewer, John C.
, p. 1245 - 1249 (2007/10/02)
The rates of reduction of a series of 1-(Z-benzyl)nicotinonitrile cations by a series of 1-(X-benzyl)-1,4-dihydronicotinamides have been studied at 25 deg C in 20percent CH3CN - 80percent H2O (pH 7.0 (5 mM phosphate), ionic strength 1.0 (KCl)).Spectral st
