Synthesis of 5(6H)-Phenanthridones Using Diels-Alder Reaction of 3-Nitro-2(1H)-quinolones Acting as Dienophiles
スポンサーリンク
概要
- 論文の詳細を見る
Diels-Alder reactions of 3-nitro-2(1H)-quinolones with 1,3-butadiene derivatives were carried out to give the phenanthridone derivatives under both atmospheric and high pressure conditions. Furthermore, the reactivity of 3-substituted 2(1H)-quinolones acting as a dienophile with 2,3-dimethyl-1, 3-butadiene was examined using molecular orbital (MO) calculation.
- 公益社団法人日本薬学会の論文
- 2006-02-01
著者
-
FUJITA Reiko
Tohoku Pharmaceutical University
-
Fujita R
Tohoku Pharmaceutical University
-
Fujita R
Department Of Chemistry School Of Liberal Arts And Sciences Iwate Medical University
-
MATSUZAKI Hisao
Tohoku Pharmaceutical University
-
YOSHISUJI Toshiteru
Tohoku Pharmaceutical University
-
WAKAYANAGI Sota
Tohoku Pharmaceutical University
-
WAKAMATSU Hideaki
Tohoku Pharmaceutical University
-
Matsuzaki H
Tohoku Pharmaceutical University
関連論文
- Reaction of 1-Alkylthioisoquinolinium Salts with Active Methylene Compounds
- Novel Synthesis of Pyrrolo[2,1-a]-isoquinnoline Using the Reaction of Isoquinolinium Salts with Active Methylene Compounds
- Electrophysiological and Pharmacological Characterization of the K_ Channel Involved in the K^+-Current Responses to FSH and Adenosine in the Follicular Cells of Xenopus Oocyte
- Augmenting Effect of Serotonin on the Voltage-Dependent Ca^ Current and Subsequently Activated K^+ Current in Aplysia Neurons
- The small GTP-binding protein RhoA regulates serotonin-induced Na^+-current response in the neurons of Aplysia
- Blockade of ionotropic receptor responses by progesterone in the ganglion cells of Aplysia
- ATP suppresses the K^+ current responses to FSH and adenosine in the folliculer cells of Xenopus oocyte (Xenopus oocyte 卵胞細胞においてFSHおよびアデノシンで発生するK^+電流応答はATP受容体刺激によって抑制される)
- 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
- Aromatase Inhibition by 4β, 5β-Epoxides of 16α-Hydroxyandrostenedione and Its 19-Oxygenated Analogs, Potential Precursors of Estriol Production in the Feto-Placental Unit
- 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
- Cell Death Mode Switch from Necrosis to Apoptosis in Brain