Novel Synthesis of Pyrrolo[2,1-a]-isoquinnoline Using the Reaction of Isoquinolinium Salts with Active Methylene Compounds

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概要

• 論文の詳細を見る
• Japan Institute of Heterocyclic Chemistryの論文

著者

• Watanabe Noriyuki

  Tohoku Pharmaceutical University

• FUJITA Reiko

  Tohoku Pharmaceutical University

• TOMISAWA Hiroshi

  Tohoku Pharmaceutical University

• Fujita R

  Tohoku Pharmaceutical University

• Fujita R

  Department Of Chemistry School Of Liberal Arts And Sciences Iwate Medical University

• Tomisawa 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
• Cycloadditions of 1-Substituted 1,3-Butadienes with 4- or 3-Substituted 2(lH)-Quinolones Acting as Dienophiles
• 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

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