78497-34-4Relevant academic research and scientific papers
Efficient synthesis of 3,5-dicarbamoyl-1,4-dihydropyridines from pyridinium salts: Key molecules in understanding NAD(P)+/NAD(P)H pathways
Mellini, Paolo,De Vita, Daniela,Di Rienzo, Barbara,La Rosa, Salvatore,Padova, Alessandro,Scipione, Luigi,Tortorella, Silvano,Friggeri, Laura
, p. 221 - 226 (2015/01/30)
3,5-Dicarbamoyl-1,4-dihydropyridines were prepared in high yields using a green protocol by reduction of the corresponding pyridinium salts in aqueous buffered sodium dithionite solutions. The pH value is a fundamental parameter for the reduction step and depends on the nature of substituent groups at positions 1, 3, and 5 of the pyridinium salts. These 3,5-dicarbamoyl dihydropyridines show a lower tendency towards oxidation and a higher stability than N-benzyl-3-carbamoyl-1,4-dihydropyridine at low pH values.
Structure of the dimers arising from one-electron electrochemical reduction of pyridinium salts 3,5-disubstituted with electron-withdrawing groups
Carelli, Vincenzo,Liberatore, Felice,Tortorella, Silvano,Di Rienzo, Barbara,Scipione, Luigi
, p. 542 - 547 (2007/10/03)
One-electron electrochemical reduction of the salts 1-benzyl-3,5-bis(methylcarbamoyl)pyridinium bromide 3a and 1-benzyl-3,5-dicarbamoylpyridinium bromide 3b yields mixtures of four isomeric dimers, as shown by HPLC analysis and mass spectrometry. 1/
