後藤 義一 | Chemistry Research Laboratories
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概要
関連著者
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後藤 義一
Chemistry Research Laboratories
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後藤 義一
Pharmaceutical Research Laboratories I Pharmaceutical Research Division Takeda Chemical Industries L
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石原 雄二
Chemistry Research Laboratories
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石原 雄二
Pharmaceutical Research Laboratories I Pharmaceutical Research Division Takeda Chemical Industries L
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吉岡 晃一
Central Research Division, Takeda Chemical Industries, Ltd.
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吉岡 晃一
Central Research Division Takeda Chemical Industries Ltd.
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平賀 謙太郎
武田薬品工業株式会社中央研究所
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平賀 謙太郎
Chemical Research Laboratories Research & Development Division Takeda Chemical Industries Ltd.
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後藤 義一
武田薬品工業(株)中央研究所
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三木 卓一
武田薬品工業株式会社中央研究所
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吉岡 晃一
Chemical Research Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
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三木 卓一
Chemical Research Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
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加藤 浩紀
Biology Research Laboratories Research And Development Division Takeda Chemical Industries Ltd.
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松本 辰美
Chemistry Research Laboratories
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清田 義弘
Biology Research Laboratories:research And Development Division Takeda Chemical Industries Ltd.
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朝子 典彦
Chemical Research Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
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宮本 政臣
Pharmaceutical Research Laboratories I Pharmaceutical Research Division Takeda Chemical Industries L
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大川 滋紀
Chemistry Research Laboratories
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寺尾 孝士
Chemistry Research Laboratories
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村上 守生
Chemistry Research Laboratories
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行正 秀文
Chemistry Research Laboratories Research And Development Division Takeda Chemical Industries Ltd.
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宮本 政臣
Biology Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd.,
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村上 守生
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
著作論文
- Synthesis of Isoindolo[2,1-a]quinoline Derivatives and Their Effects on N_2-Induced Hypoxia
- Total Synthesis of 13β-Allylgonanes. III
- Total Synthesis of 13β-Allylgonanes. II
- Total Synthesis of 13β-Allylgonanes. I. Synthesis of dl-17α-Ethynyl-17β-hydroxy-13β-allylgon-4-en-3-one
- Reduction of 2,3,5-Trimethyl-6-(3-pyridylmethyl)-1,4-benzoquinone by PB-3c Cells and Biological Activity of Its Hydroquinone
- Central Cholinergic Agents. III. Synthesis of 2-Alkoxy-2,8-diazaspiro[4.5]decane-1,3-diones as Muscarinic Agonists
- Central Cholinergic Agents. II. Synthesis and Acetylcholinesterase Inhibitory Activities of N-[ω-[N-Alkyl-N-(phenylmethyl)amino]alkyl]-3-arylpropenamides
- Central Cholinergic Agents. I. Potent Acetylcholinesterase Inhibitors, 2-[ω-[N-Alkyl-N-(ω-phenyl-alkyl)amino]alkyl]-1H-isoindole-1,3(2H)-diones, Based on a New Hypothesis of the Enzyme's Active Site