Cycloaddition of 2-pyridones having an electron-withdrawing group
スポンサーリンク
概要
著者
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FUJITA Reiko
Tohoku Pharmaceutical University
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Fujita R
Tohoku Pharmaceutical University
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Fujita R
Department Of Chemistry School Of Liberal Arts And Sciences Iwate Medical University
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Hoshino M
Tohoku Pharmaceutical University
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Matsuzaki H
Tohoku Pharmaceutical University
関連論文
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- Diels-Alder Reaction of 2(1H)-Pyridones Acting as Dienes
- Cycloaddition of 2-pyridones having an electron-withdrawing group
- Cyclization of 1-Benzyl-1,2-dihydro-2-(substituted methylene)quinolines to Pyrrolo [1,2-a] quinoline Derivatives
- Cycloaddition of 2(1H)-Pyridones Having a Methoxycarbonyl Group to 1, 3-Butadiene Derivatives
- Synthesis of Isoquinoline Derivatives by Diels-Alder Reactions of 2(1H)-Pyridones Having an Electron-withdrawing Group with Methoxy-1,3-butadienes
- Diels-Alder Reaction of 1, 3-Butadiene Derivatives with 1-Methyl-2(1H)-quinolones Having an Electron-Withdrawing Group at the 4-Position
- Diels-Alder Cycloadditions of 2(1H)-Quinolones Having an Electron-Withdrawing Group at the 3-Position Acting as Dienophiles with Dienes
- Diels-Alder Reactions of Nitro-2(1H)-pyridones with 2, 3-Dimethyl-1, 3-butadiene
- Synthesis of Phenanthridones Using Diels-Alder Reactions of 4-Substituted 2(1H)-Quinolones Acting as Dienophiles
- Novel Diels-Alder Reaction of 4-Nitro-1(2H)-isoquinolones
- Cycloadditions of 1-Substituted 1,3-Butadienes with 4- or 3-Substituted 2(lH)-Quinolones Acting as Dienophiles
- Studies on the 1,4-Oxazepine Ring Formation Reaction Using the Molecular Orbital Method
- Studies on the Reaction of Benzo[X]quinoline N-Oxides (X=f, h, and g)with Methylsulfinyl Carbanion Using the Semi-empirical Molecular Orbital Method. Liberation of the N-Oxide Group
- Isotope Effects in the Reaction of Benzo[h]quinoline N-Oxides with Methylsulfinyl Carbanion Examined by ab Initio Molecular Orbital Methods
- Synthesis of 5(6H)-Phenanthridones Using Diels-Alder Reaction of 3-Nitro-2(1H)-quinolones Acting as Dienophiles
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