20557-70-4Relevant academic research and scientific papers
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.
NMR Properties and Synthesis of Ring-methylated 1,4-Dihydronicotinamides and the Corresponding Pyridinium Salts. Correlation of NMR with Ab Initio STO-3G Results
Bossaerts, Jan D.,Dommisse, Roger A.,Alderweireldt, Frank C.,Geerlings, Paul
, p. 2360 - 2384 (2007/10/02)
The synthesis of a series of ring-methylated 1-alkyl-1,4-dihydronicotinamides and the corresponding pyridinium salts is described.Their NMR properties involving aromatic-ring-shielding anisotropy, due to ring current effects, are discussed and compared with electron populations calculated from STO-3G results.
Steric and Electronic Effects of Methyl Substitutents at the 2- and 6-Positions on N-Benzyl-1,4-dihydronicotinamide
Takeda, Jun,Ohta, Shigeru,Hirobe, Masaaki
, p. 2661 - 2667 (2007/10/02)
N-Benzyl-1,4-dihydronicotinamides having 2-methyl, 6-methyl and 2,6-dimethyl substituents were prepared and their reactivities toward an activated carbonyl compound (hexachloroacetone) were investigated.The reaction rates were especially enhanced for the
