The reaction of nitrosonium (NO+) with Schiff bases produced diazonium salts and aldehydes in good yield. The reaction is assumed to be an electrophilic reaction of nitrosonium with imines via a four-member ring inter...The reaction of nitrosonium (NO+) with Schiff bases produced diazonium salts and aldehydes in good yield. The reaction is assumed to be an electrophilic reaction of nitrosonium with imines via a four-member ring intermediate.展开更多
The oxidation on 1,4-substituted Hantzsch 1,4-dihydropyridines with nitrosonium tetrafluoroborate (NO+BF4-) in acetonitrile gave Hantzsch pyridines in good yields. In some cases the dealkylation occurred. The evidence...The oxidation on 1,4-substituted Hantzsch 1,4-dihydropyridines with nitrosonium tetrafluoroborate (NO+BF4-) in acetonitrile gave Hantzsch pyridines in good yields. In some cases the dealkylation occurred. The evidences to draw the mechanism were presented.展开更多
3,4-Dihydropyrimidin-2(1H)-ones (DHPMs) were oxidized with 1.2 equiv, of nitrosonium tetrafluoroborate (NO^+BF4^-) to pyrimidin-2(1H)-ones in acetonitrile at room temperature in high yields.
文摘The reaction of nitrosonium (NO+) with Schiff bases produced diazonium salts and aldehydes in good yield. The reaction is assumed to be an electrophilic reaction of nitrosonium with imines via a four-member ring intermediate.
文摘The oxidation on 1,4-substituted Hantzsch 1,4-dihydropyridines with nitrosonium tetrafluoroborate (NO+BF4-) in acetonitrile gave Hantzsch pyridines in good yields. In some cases the dealkylation occurred. The evidences to draw the mechanism were presented.
基金Project No.20572040 was supported by National Natural Science Foundation of China
文摘3,4-Dihydropyrimidin-2(1H)-ones (DHPMs) were oxidized with 1.2 equiv, of nitrosonium tetrafluoroborate (NO^+BF4^-) to pyrimidin-2(1H)-ones in acetonitrile at room temperature in high yields.