寺島 孜郎 | Sagami Chemical Research Center
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概要
関連著者
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寺島 孜郎
Sagami Chemical Research Center
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寺島 孜郎
相模中研
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松本 光代
Sagami Chemical Research Center
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大崎 正子
Sagami Chemical Research Center
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伊藤 芳雄
Sagami Chemical Research Center
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木村 芳一
相模中研
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鈴木 三千代
Sagami Chemical Research Center
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木村 芳一
Sagami Chemical Research Center
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大崎 正子
School of Pharmaceutical Sciences, Toho University
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大崎 正子
School Of Pharmaceutical Sciences Toho University
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竹本 佳司
Faculty Of Pharmaceutical Sciences Osaka University
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Takemoto Yoshiji
Faculty Of Pharmaceutical Sciences Osaka University
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Takemoto Y
Graduate School Of Pharmaceutical Sciences Kyoto University
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川崎 元士
相模中研
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竹本 佳司
Sagami Chemical Research Center
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川崎 元士
Sagami Chemical Research Center
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原田 弘
Central Research Laboratories, Kissei Pharmaceutical Co., Ltd.,
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上條 哲聖
Central Research Laboratories, Kissei Pharmaceutical Co., Ltd.,
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上條 哲聖
キッセイ薬品工業株式会社中央研究所
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上条 哲聖
キッセイ薬品工業中央研究所
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原田 弘
Central Research Laboratories Kissei Pharmaceutical Co. Ltd.
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山田 薫
相模中研
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鈴木 康隆
Exploratory Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
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中谷 和彦
相模中研:(現)大阪市立大学理学部
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松田 冬彦
相模中研:(現)北海道大学理学部
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山田 薫
Sagami Chemical Research Center
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松田 冬彦
Sagami Chemical Research Center
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小林 祐子
Sagami Chemical Research Center
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寺島 孜郎
(財)相模中央化学研究所
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中谷 和彦
Sagami Chemical Research Center
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寺島 孜郎
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)sagami Chemical Research Cen
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鈴木 康隆
Faculty of Pharmaceutical Sciences, University of Tokyo
著作論文
- 14-Fluoroanthracyclines. : Novel Syntheses and Antitumor Activity
- Novel Synthesis of Three Types of C-Terminal Components of Renin Inhibitors from Unnatural(2S, 3S)-Tartaric Acid
- A Highly Stereoselective Synthesis of (3S, 4S)-Statine and (3S, 4S)-Cyclohexylstatine
- Synthesis of Novel 13-Methyl-13-dihydroanthracyclines
- Synthesis of 4-Demethoxyanthracyclines Carrying a Lipophilic Alkanoyl Group at the C_9-Position
- Asymmetric Reduction of 4-Phenyl-3 (E)-buten-2-one by Using Lithium Aluminum Hydride Partially Decomposed with (-)-N-Methylephedrine and Achiral Secondary Amine
- Lithium Aluminum Hydride Partially Decomposed with (-)-N-Methylephedrine and 2-Alkylaminopyridine : An Improved Chiral Hydride Useful for the Practical Asymmetric Reduction of Achiral Cyclic Ketones
- Novel Ethynylcerium(III) Reagents as Efficient Tools for Constructing the α-Hydroxy Methyl Ketone Moiety of Anthracyclinones
- Synthesis of Novel Monobactams Bearing an (R)-1-Hydroxyethyl Group and an (S)-1-Carbamoyl-oxyethyl Group at the C_-Positions