田中 博道 | School of Pharmaceutical Sciences, Showa University
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概要
関連著者
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田中 博道
School of Pharmaceutical Sciences, Showa University
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宮坂 貞
School of Pharmaceutical Sciences, Showa University
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宮坂 貞
昭和大学大学院薬学研究科医療薬学専攻
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宮坂 貞
School Of Pharmaceutical Sciences Showa University
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早川 弘之
School of Pharmaceutical Sciences, Showa University
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山口 健太郎
School of Pharmaceutical Sciences, Showa University
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松田 彰
Faculty Of Pharmaceutical Sciences Hokkaido University
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山口 健太郎
School Of Pharmaceutical Sciences Showa University
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松田 彰
School of Pharmaceutical Sciences, Showa University
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鈴木 雅博
Hanno Research Center Chemistry Lab. Taiho Pharmaceutical Co. Ltd.
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鈴木 雅博
School of Pharmaceutical Sciences, Showa University
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山口 健太郎
千葉大学分析センター
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飯高 洋一
Faculty of Pharmaceutical Sciences, The University of Tokyo
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内田 祐子
School Of Pharmaceutical Sciences Showa University
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伊藤 直子
School of Pharmaceutical Sciences, Showa University
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中島 政子
School of Pharmaceutical Sciences, Showa University
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高井 富美
School of Pharmaceutical Sciences, Showa University
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中島 政子
School Of Pharmaceutical Sciences Showa University
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篠崎 操
School of Pharmaceutical Sciences, Showa University
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飯島 秀治
School of Pharmaceutical Sciences, Showa University
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芦沢 広
School Of Pharmaceutical Sciences Showa University
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原口 一広
School of Pharmaceutical Sciences, Showa University
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飯高 洋一
Faculty Of Pharmaceutical Sciences The University Of Tokyo
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伊藤 直子
School Of Pharmaceutical Sciences Showa University
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高井 富美
School Of Pharmaceutical Sciences Showa University
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篠崎 操
School Of Pharmaceutical Sciences Showa University
著作論文
- Synthesis of 5-Carbon-Substituted 1-β-D-Ribofuranosylimidazole-4-carboxamides via Lithiation of a Primary Carboxamide(Organic,Chemical)
- REACTION OF ORGANOMETALLIC REAGENTS WITH 2'- AND 3'-KETOURIDINE DERIVATIVES : SYNTHESIS OF URACIL NUCLEOSIDES BRANCHED AT THE 2'- AND 3'-POSITIONS(Communications to the Editor)
- Diethylaminosulfur Trilfluoride (DAST) as a Fluorinating Agent of Pyrimidine Nucleosides Having a 2', 3'-Vicinal Diol System
- SYNTHESIS AND BIOLOGICAL ACTIVITIES OF 5-SUBSTITUTED 6-PHENYLTHIO AND 6-IODOURIDINES, A NEW CLASS OF ANTILEUKEMIC NUCLEOSIDES
- A SIMPLIFIED SYNTHESIS OF 8-SUBSTITUTED PURINE NUCLEOSIDES VIA LITHIATION OF 6-CHLORO-9-(2,3-O-ISOPROPYLIDENE-β-D-RIBOFURANOSYL) PURINE
- Introduction of an Alkyl Group into the Sugar Portion of Uracilnucleosides by the Use of Gilman Reagents
- Direct C-8 Lithiation of Naturally-Occurring Purine Nucleosides. A Simple Method for the Synthesis of 8-Carbon-Substituted Purine Nucleosides(Organic,Chemical)
- A NOVEL AND REGIOSPECIFIC ROUTE TO 5-ACYLURIDINES VIA AN AMIDE α-ANION DERIVED FROM 5,6-DIHYDROURIDINE
- FIRST EXCEPTIONS TO THE"IMBACH RULE"FOR β-D-RIBOFURANOSYL NUCLEOSIDES
- Synthesis of 6-Aroyluridine from Uridine via Regiospecific Lithiation