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
An efficient Michael addition of indoles to unsaturated enones, such as chalcones and β-nitrostyrenes, was achieved in the presence of a catalytic amount of nitrosonium tetrafluoroborate in ethyl ether. 2007 Long M...An efficient Michael addition of indoles to unsaturated enones, such as chalcones and β-nitrostyrenes, was achieved in the presence of a catalytic amount of nitrosonium tetrafluoroborate in ethyl ether. 2007 Long Min Wu. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.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.
Efficient nitrosonium （NO＋）-initiated aza-Diels-Alder reactions of N-arylimines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran allowed access to furano[3,2-c]- or pyrano[3,2-c]quinolines. A mixture of cis and trans-...Efficient nitrosonium （NO＋）-initiated aza-Diels-Alder reactions of N-arylimines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran allowed access to furano[3,2-c]- or pyrano[3,2-c]quinolines. A mixture of cis and trans-quinoline isomers was obtained in various ratios and yields.展开更多
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.
基金Project No. 20572040 was supported by National Natural Science Foundation of China.
文摘An efficient Michael addition of indoles to unsaturated enones, such as chalcones and β-nitrostyrenes, was achieved in the presence of a catalytic amount of nitrosonium tetrafluoroborate in ethyl ether. 2007 Long Min Wu. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
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.
基金Project supported by the National Natural Science Foundation of China （No. 20572040）.
文摘Efficient nitrosonium （NO＋）-initiated aza-Diels-Alder reactions of N-arylimines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran allowed access to furano[3,2-c]- or pyrano[3,2-c]quinolines. A mixture of cis and trans-quinoline isomers was obtained in various ratios and yields.
