冨士 薫 | Institute For Chemical Research Kyoto University
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概要
関連著者
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冨士 薫
Institute For Chemical Research Kyoto University
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藤田 栄一
Osaka University Of Pharmaceutical Sciences
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藤田 栄一
京都大学化学研究所
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野出 学
Institute For Chemical Research Kyoto University
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野出 学
Kyoto Pharmaceutical University
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藤田 栄一
Institute for Chemical Research, Kyoto University
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藤田 栄一
Institute For Chemical Research Kyoto University
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藤田 榮一
Osaka University of Pharmaceutical Sciences
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Fuji Kaoru
Institute For Chemical Research Kyoto University
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Node Manabu
Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U
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Node Manabu
Kyoto Pharmaceutical Univ.
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田中 圭
静岡県大 薬
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伊藤 望
Research Laboratories Nippon Shoji Kaisha Ltd.
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FUJI KAORU
Institute for Chemical Research, Kyoto University
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田中 圭
京都大学薬学部
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山田 敏英
Tokushima Research Institute Otsuka Pharmaceutical Co. Ltd.
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冨士 薫
京都大学化学研究所
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川端 猛夫
京都大学化学研究所
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田中 圭
Institute for Chemical Research, Kyoto University
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山田 敏英
Institute for Chemical Research, Kyoto University
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川端 猛夫
京大化研
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Kinoshita T
Exploratory Research Laboratoeis Fujisawa Pharmaceutical Co. Ltd.
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正木 幸雄
Gifu Pharmaceutical University
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太田 敬一郎
Institute For Chemical Research Kyoto University
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城 始勇
Research And Development Division Rigaku Industrial Corporation
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孫 漢董
中国科学院昆明植物研
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TSUBAKI Kazunori
Institute for Chemical Research, Kyoto University
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川端 猛夫
Institute for Chemical Research, Kyoto University
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佐井 みどり
Faculty of Pharmaceutical Sciences, Setsunan University
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藤田 榮一
Institute for Chemical Research, Kyoto University
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李 波
Kunming Institute Of Botany Academia Sinica
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Tsubaki K
Institute For Chemical Research Kyoto University
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正木 幸雄
岐阜薬科大学
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武田 節夫
Tokushima Institute, Taiho Pharmaceutical Co., Ltd.,
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武田 節夫
Research Institute, Taiho Pharmaceutical Co., Ltd.,
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新宮 徹朗
神戸学院大薬
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別所 清
Institute For Chemical Research Kyoto University
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西出 喜代治
京都薬科大学薬品製造学教室 創薬科学フロンティア研究センター
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高須 清誠
京都大学大学院薬学研究科
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中井 博
Shionogi Research Laboratories
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Shiro M
Rigaku Corp. Tokyo
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城 始勇
Shionogi Research Laboratory, Shionogi & Co.
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長尾 善光
Institute for Chemical Research, Kyoto University
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落合 正仁
Institute for Chemical Research, Kyoto University
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多賀 徹
京大・薬
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横井 利夫
神戸学院大学薬学部薬化学講座
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孫 漢董
Kunming Institute of Botany, Academia Sinica
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内田 逸郎
Exploratory Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.,
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徐 海剣
Chemical Institute Kyoto University
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孫 漢董
Kunming Institute Of Botany Academia Sinica
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Takasu Kiyosei
Institute Of Chemical Research Kyoto University
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伊藤 望
Institute for Chemical Research, Kyoto University
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〓 小江
Institute For Chemical Research Kyoto University
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Hao X‐j
Kunming Institute Of Botany Academia Sinica
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新宮 徹朗
神戸学院大学薬学部薬化学講座
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Shingu K
Kumamoto Univ. Kumamoto Jpn
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新宮 徹朗
神院大・薬
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新宮 徹朗
京都大学薬学部
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NURUZZAMAN Mohammad
Institute for Chemical Research, Kyoto University
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西出 喜代治
Institute for Chemical Research, Kyoto University
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渡辺 宏二
Institute for Chemical Research, Kyoto University
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Shingu K
School Of Pharmacy Kobe Gakuin University
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長尾 善光
Institute For Chemical Research Kyoto University
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多賀 徹
京大・院薬・薬品分子構造
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中井 博
Shionogi Research Laboratories Shionogi & Co. Ltd.
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落合 正仁
Institute For Chemical Research Kyoto University
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内田 逸郎
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
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Node M
Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U
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Node Manabu
Department Of Pharmaceutical Manufacturing Chemistry Kyoto Pharmaceutical University
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采見 憲男
Tokushima Institute Taiho Pharmaceutical Co. Ltd.
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釆見 憲男
Research Laboratory Taiho Pharmaceutical Co. Ltd.
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Shiro M
Rigaku Corporation
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Nuruzzaman Mohammad
Institute For Chemical Research Kyoto University
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武田 節夫
Tokushima Institute Taiho Pharmaceutical Co. Ltd.
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渡辺 宏二
Institute For Chemical Research Kyoto University
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OTSUBO Tadamune
Institute for Chemical Research, Kyoto University
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周 俊
Kunming Institute of Botany, the Chinese Academy of Science
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宮嶋 孝一郎
Faculty of Pharmaceutical Sciences, Kyoto University
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阿部 光幸
国立京都病院
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野出 学
京都薬科大学薬品製造
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米田 文郎
Faculty of Pharmaceutical Sciences, Kyoto University
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多賀 徹
Faculty of Pharmaceutical Sciences, Kyoto University
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Kinoshita Takayoshi
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
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新宮 徹朗
Faculty of Pharmaceutical Sciences, Kobe Gakuin University
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三輪 嘉尚
Faculty of Pharmaceutical Sciences, Kyoto University
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周 俊
Kunming Institute Of Botany The Chinese Academy Of Science
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半田 哲郎
京大・薬
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芝本 雄太
京都大学放射線科
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宮本 寿
大塚製薬株式会社微生物研究所
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半田 哲郎
Faculty of Pharmaceutical Sciences, Kyoto University
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母里 知之
Department Of Radiation Oncology School Of Medicine Tokai University
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秋山 泰身
Faculty of Pharmaceutical Sciences, Kyoto University
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宮嶋 孝一郎
大阪薬科大学招聘教授
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秋山 泰身
Faculty Of Pharmaceutical Science Kyoto University
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西本 清一
京都大学工学研究科
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小松 裕明
Division of Drugs, National Institute of Health Science, Osaka Branch
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岡田 敏史
Division of Drugs, National Institute of Health Science, Osaka Branch
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藤多 哲朗
徳島大学薬学部
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半田 哲郎
Faculty Of Pharmacy Kyoto University
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佐野 茂樹
Institute for Chemical Research, Kyoto University
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西本 清一
Department of Hydrocarbon Chemistry, Faculty of Engineering, Kyoto University
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鍵谷 勤
Department of Hydrocarbon Chemistry, Faculty of Engineering, Kyoto University
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MURAYAMA Chieko
Department of Radiation Oncology, School of Medicine, Tokai University
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芝本 雄太
Department of Radiology, Faculty of Medicine, Kyoto University
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笹井 啓資
Department of Radiology, Faculty of Medicine, Kyoto University
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阿部 光幸
Department of Radiology, Faculty of Medicine, Kyoto University
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谷口 清
New Drug Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
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谷口 清
Institute for Chemical Research, Kyoto University
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安 美子
Institute for Chemical Research, Kyoto University
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水地 真樹
Institute for Chemical Research, Kyoto University
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新宮 徹朗
School of Pharmacy, Kobe Gakuin University
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横井 利夫
神戸学院大学薬学部
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横井 利夫
Faculty Of Pharmaceutical Sciences Kobe-gakuin University
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孫 漢董
中国科学院昆明植物研究所
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栗山 馨
Shionogi Research Laboratory
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宮本 寿
Institute for Chemical Research, Kyoto University
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笹井 啓資
Department Of Radiology Faculty Of Medicine Kyoto University
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佐野 茂樹
徳島大学薬学部
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岡田 敏史
国立衛研・大阪
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Okada S
Division Of Drugs Osaka Branch National Institute Of Health Sciences
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Katoh Takahiro
Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U
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Kohno Michiaki
School Of Pharmaceutical Sciences Nagasaki University
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青木 宏光
Faculty Of Pharmaceutical Sciences Kyoto University
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梶本 哲也
京都薬大
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冨士 薫
京大・化研
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藤多 哲朗
Institute for Chemical Research, Kyoto University
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中村 薫竹
Institute for Chemical Research, Kyoto University
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岩田 辰夫
Shionogi Research Laboratories, Shionogi & Co., Ltd.
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村田 弘之
Institute for Chemical Research, Kyoto University
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中村 恵宣
Faculty of Pharmaceutical Sciences, Kyoto University
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角 昭久
Institute for Chemical Research, Kyoto University
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新宮 徹朗
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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Asakawa Naoyuki
Institute For Chemical Research Kyoto University
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永久 良輝
Faculty of Pharmaceutical Sciences, Kyoto University
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TANAKA Kiyoshi
School of Pharmaceutical Sciences, University of Shizuoka
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YOSHIDA Masato
Institute for Chemical Research, Kyoto University
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YANG Xiao-Shen
Institute for Chemical Research, Kyoto University
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浪花 佳光
Institute for Chemical Research, Kyoto University
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大森 富士海
Institute for Chemical Research, Kyoto University
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徐 海剣
Institute for Chemical Research, Kyoto University
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辰巳 煕
Research Laboratories, Nippon Shoji Kaisha, Ltd.,
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今堀 秀和
Research Laboratories, Nippon Shoji Kaisha, Ltd.,
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稲葉 実
Cancer Chemotherapy Center, Japanese Foundation for Cancer Research
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〓 尚珍
Institute for Chemical Research, Kyoto University
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WANG Zhao-Quan
Institute for Chemical Research, Kyoto University
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XU Feng-Ming
Anhui Provincial Institute of Medical Sciences
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HU Hui-Ping
Anhui Provincial Institute of Medical Sciences
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采見 憲男
Research Laboratory, Taiho Pharmaceutical Co., Ltd.,
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WATSON William
FASTBIOS Laboratory, Department of Chemistry, Texas Christian University
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GROSSIE David
FASTBIOS Laboratory, Department of Chemistry, Texas Christian University
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ZABEL Volker
FASTBIOS Laboratory, Department of Chemistry, Texas Christian University
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陳 洫英
Kunming Institute of Botany, Academia Sinica
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釆見 憲男
Research Laboratory, Taiho Pharmaceutical Co., Ltd.
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太田 啓一郎
Institute for Chemical Research, Kyoto University
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川端 武夫
Institute for Chemical Research, Kyoto University
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中村 恵宣
Faculty Of Pharmaceutical Science Kyoto University
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李 波
京大・化研
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田中 圭
京大・化研
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梶本 哲也
Institute for Chemical Research, Kyoto University
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Wang Zhao-quan
Institute For Chemical Research Kyoto University
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WATANABE Yukari
Institute for Chemical Research, Kyoto University
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OHTSUBO Tadamune
Institute for Chemical Research, Kyoto University
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HAMAJIMA Yoshio
Institute for Chemical Research, Kyoto University
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田中 圭
静岡県立大学薬学部薬品製造化学教室
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孫 常麒
Faculty of Pharmaceutical Sciences, Kyoto University
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冨士 薫
Chemical Institute, Kyoto University
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李 波
Institute for Chemical Research, Kyoto University
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多賀 徹
Academia Sinica, Kunming, Yunnan, China, and Faculty of Pharmaceutical Sciences, Kyoto University
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国嶋 崇隆
Institute for Chemical Research, Kyoto University
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城 始勇
Japan and Shionogi Research Laboratories, Shionogi & Co. Ltd.,
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Murayama Chieko
Department Of Radiation Oncology School Of Medicine Tokai University
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米田 文郎
Faculty Of Pharmaceutical Sciences Kyoto University
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芝本 雄太
名古屋市大 病院 中央放射線部
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宮嶋 孝一郎
京大・薬
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長尾 善光
徳島大学薬学部
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阿部 光幸
Department Of Radiology Faculty Of Medicine Kyoto University
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TAGA Tohru
Faculty of Pharmaceutical Sciences, Kyoto University
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宮嶋 孝一郎
京都大学薬学部
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市川 皇陛
Institute for Chemical Research, Kyoto University
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多賀 徹
Faculty Of Pharmaceutical Sciences Kyoto University
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〓 尚珍
Institute For Chemical Research Kyoto University
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Taga Tohru
Faculty Of Pharmaceutical Sciences Kyoto University
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国嶋 崇隆
Institute For Chemical Research Kyoto University
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永久 良輝
Faculty Of Pharmaceutical Sciences Kyoto University
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浪花 佳光
Institute For Chemical Research Kyoto University
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小松 裕明
Division Of Drugs Osaka Branch National Institute Of Health Sciences
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大森 富士海
Institute For Chemical Research Kyoto University
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KAWADA MITSURU
Pharmaceutical Research Division, Takeda Chemical Industries Ltd.
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三輪 嘉尚
Faculty Of Pharmaceutical Sciences Kyoto University
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Zabel Volker
Fastbios Laboratory Department Of Chemistry Texas Christian University
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Yang Xiao-shen
Institute For Chemical Research Kyoto University
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孫 常麒
Faculty Of Pharmaceutical Sciences Kyoto University
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Nuruzzaman M
Institute For Chemical Research Kyoto University
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Grossie David
Fastbios Laboratory Department Of Chemistry Texas Christian University
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Kawada Mitsuru
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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Bando Masahiko
Otsuka Parmaceutical Co. Ltd.
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Watson William
Fastbios Laboratory Department Of Chemistry Texas Christian University
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MUKOYOSHI Koichiro
Institute for Chemical Research, Kyoto University
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Watanabe Yukari
Institute For Chemical Research Kyoto University
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Hamajima Yoshio
Institute For Chemical Research Kyoto University
著作論文
- RADIOSENSITIZING HYPOXIC CELLS WITH NEW 3-NITRO-1,2,4-TRIAZOLE DERIVATIVES IN VITRO AND IN VIVO
- Diastereoselectivity in Addition of Methylmagnesium Halide to Benzoylformate of Chiral 1,1'-Binaphthalene-2,2'-diol
- Chiral Piperazines as Catalysts for the Enantioselective Addition of Diethylzinc to Aldehydes
- The Absolute Configuration of Enmein Transformation of Enmein into (-)-Kaurane
- Lythraceous Alkaloids. XIV. Kinetic Equalization of Carbon-13 Nuclear Magnetic Resonance Chemical Shifts in N, O-Dimethyllythranidine, a Cyclophane Bearing Asymmetric Carbon Atoms
- Lythraceous Alkaloids. XIII. X-Ray Determination of the Molecular Structures of O-Methyllythranidine N, O, O-Triformate, 22-Bromolythranine N, O, O-Triacetate, and O-Methyldeacetyllythramine
- Lythraceous Alkaloids. XII. Circular Dichroism Studies on Lythranine-Type Alkaloids
- Lythraceous Alkaloids. X. Alkaloids of Lagerstroemia subcostata and L. favriei : A Contribution to the Chemotaxonomy
- Lythraceous Alkaloids. II. The Structure of O-Methyllythranidine
- Lythraceous Alkaloids. I. Characterization of the Novel Alkaloids, Lythranine, Lythranidine, and Lythramine isolated from Lythrum anceps MAKINO
- HYBRIDIZATION OF OLIGODEOXYNUCLEOTIDE WITH REXOD COENZYME MODEL; SYNTHESIS AND PROPERTIES OF THYMIDINE DECAMERS COVALENTLY LINKED TO 5-DEAZAFLAVIN
- Use of 1,1'-Binaphthalene-8,8'-diol as a Chiral Auxiliary for Asymmetric Michael Addition. Application to the Syntheses of Turmeronol A and B
- ENHANCED REACTIVITY OF ZINC ENOLATES OVER LITHIUM ENOLATES IN ASYMMETRIC NITROOLEFINATION
- Design and Synthesis of Antitumor Compounds Based on the Cytotoxic Diterpenoids from the Genus Rabdosia
- A Chiral Synthesis of a Unique Secodehydroabietane from Tall Oil
- Terpenoids. LIV. : The Structures of Rabdoinflexins A and B, New Diterpenoids from Rabdosia inflexa (THUNB.) HARA
- Terpenoids. LIII. : Antitumor Activity of Trichorabdals and Related Compounds
- Terpenoids. LII. : The Structures of Trichorabdal F, Trichorabdal G Acetate, and Trichorabdal H. A Comment on the Structure of Shikodonin
- Terpenoids. LI. : Structures of Antitumor Diterpenoids, Trichorabdals A-E, Isolated from Rabdosia trichocarpa
- THE STRUCTURES OF FOUR NEW DITERPENE ALKALOIDS, SPIRAMINES A, B, C, AND D(Communications to the Editor)
- Terpenoids. L. Antitumor Activity of Diterpenoids from Rabdosia shikokiana var. occidentalis
- Terpenoids. XLVIII. New Diterpenoids from Rabdosia shikokiana var. occidentalis
- Hard Acid and Soft Nucleophile System. VII. A Convenient Reduction of Functionalized Polyarenes to Parent Polyarenes
- RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO- AND PARA-HALOPHENOLS AND THEIR DERIVATIVES
- P-1 中国産イチイ科植物Taxus chinensisの新ジテルペノイド(ポスター発表の部)
- ON THE STRUCTURES OF SIX NEW DITERPENOIDS, TAXCHININS E, H, I, J, K AND TAXCHIN B
- SELECTIVE DEMETHYLATION OF ALIPHATIC METHYL ETHER IN THE PRESENCE OF AROMATIC METHYL ETHER WITH THE ALUMINUM CHLORIDE-SODIUM IODIDE-ACETONITRILE SYSTEM
- Terpenoids. XLIX. Reactions of Shikoccin : Oxidation, Catalytic Reduction, and Conversion into the Abietane Skeleton
- THREE NEW 8,9-SECO-ENT-KAURANE DITERPENOIDS FROM RABDOSIA SHIKOKIANA (LABIATAE)
- A Chiral Nonracemic Enolate with Dynamic Axial Chirality: Direct Asymmetric Alkylation of α-Amino Acid Derivatives (SYNTHETIC ORGANIC CHEMISTRY-Fine Organic Synthesis)
- Visualization of Molecular Length of α, ω-Diamines and Temperature by a Receptor Based on Phenolphthalein and Crown Ether (SYNTHETIC ORGANIC CHEMISTRY-Fine Organic Synthesis)
- Synthesis of Extremely Simplified Compounds Possessing the Key Pharmacophore Units of Taxol, Phenylisoserine and Oxetane Moieties
- The First Synthesis of an Optically Active Molecular Bevel Gear with Only Two Cogs on Each Wheel (SYNTHETIC ORGANIC CHEMISTRY-Fine Organic Synthesis)
- 光学活性リン試薬を用いる不斉レフィン化
- Effects of Cholesterol on the Miscibility of Synthetic Glucosamine Diesters in Lipid Bilayers and the Entrapment of Superoxide Dismutase into the Positively Charged Liposomes
- THREE NEW DITERPENOIDS FROM TAXUS CHINENSIS
- Hard Acid and Soft Nucleophile Systems. Part 13. Aluminum Chloride-Sodium Iodide-Acetonitrile System : A Very Mild Reagent for Selective Dealkylation (Commemoration Issue Dedicated to Professor Shigeo Tanimoto On the Occation of His Retirement)
- SYNTHESIS, STRUCTURE, AND SELF-OXIDATION OF ALKYNYL(PHENYL)IODONIUM PERIODATES
- Regioselective Hydroxylation in the C Ring of ent-Kaurene ; Syntheses of ent-11α-Hydroxykaurene and ent-11α-Hydroxykauren-15-one
- Hard Acid and Soft Nucleophile System. IV. Removal of Benzyl Protecting Group with Boron Trifluoride Etherate and Dimethyl Sulflide
- A Versatile Synthesis of (±)-Solenopsin A
- The First Example for Cycloenantiomeric Hexahomooxacalix[3]arenes
- The '2+1' Construction of Homooxacalix[3]arenes Possessing Different Substituents on Their Upper Rims
- Preparation of Nitroalkenes : Substitution Reaction via Addition-Elimination Using β-Nitrovinyl Sulfoxides.
- Hard Acid and Soft Nucleophile Systems. Part 12. : Regioselective Functionalization of 1,3-Dienes through the Lewis Acid Mediated Thienium Cation Diels-Alder Reaction.
- Asymmetric Diels-Alder Cycloaddition with Chiral 2-Alkylsulfinyl-1-nitroalkenes.
- PB133 ENANTIOSELECTIVE TOTAL SYNTHESES OF (+)-PODOCARPIC ACID AND RELATED DITERPENOIDS
- Addition-Elimination Strategy for Asymmetric Induction : A Chiral Sulfoxide as a Leaving Group.
- A Formal Asymmetric Synthesis of Calabar Bean Alkaloids
- New Chiral Shift Reagents, Optically Active 2,2'-Dihydroxy-1,1'-binaphthyl and 1,6-Di(o-chlorophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol.
- Conformational Difference between Mono- and Diprotonated cis-2,5-Diphenylpiperazinium Salts in the Solid State
- Conformation of 1, 4-Dineopentyl-2, 5-cis-diphenylpiperazinc and Its Diammonium Salts : Remarkable Change in Conformation Depending upon the Counter Anion
- A Total Synthesis of (-)-Physostigmine.