Tozawa Takashi | Center For Basic Research The Kitasato Institute
スポンサーリンク
概要
関連著者
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Tozawa Takashi
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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MUKAIYAMA Teruaki
Center for Basic Research, The Kitasato Institute
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YAMANE Yoshinobu
Center for Basic Research, The Kitasato Institute
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Yamane Yoshinobu
Center For Basic Research The Kitasato Institute
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FUJISAWA Hidehiko
Center for Basic Research, The Kitasato Institute
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Mukaiyama Teruaki
The Kitasato Institute Center For Basic Research
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TOZAWA Takashi
Department of Applied Chemistry, Faculty of Science, Science University of Tokyo
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Tozawa Takashi
Center For Basic Research The Kitasato Institute (tci)
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Fujisawa Hidehiko
Center For Basic Research The Kitasato Institute
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Fujisawa H
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Minowa Tomofumi
Kitasato Institute For Life Sciences Kitasato University
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MUKAIYAMA Teruaki
Kitasato Institute for Life Sciences, Kitasato University
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Mukaiyama T
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Kitasato Institute For Life Sciences Kitasato University
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Mukaiyama Teruaki
Kitasato Inst. For Life Sciences Kitasato Univ.
著作論文
- Diastereo- and Enantioselective Tandem Michael Addition and Lactonization between Silyl Enolates and α,β-Unsaturated Ketones Catalyzed by a Chiral Quaternary Ammonium Phenoxide
- Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Chiral Quaternary Ammonium Phenoxide-catalyzed Tandem Michael Addition and Lactonization
- A Convenient Method for the Synthesis of Carboxamides and Thioesters by Using Tetrakis(2-methylimidazol-1-yl)silane
- An Efficient Method for the Preparation of Carboxamides by Dehydration Condensation Using Tetrakis(1,1,1,3,3,3-hexafluoro-2-propoxy)silane
- An Effective Method for the Synthesis of Carboxamides by Using Tetrakis(pyridine-2-yloxy)silane as a Mild Coupling Reagent
- A Convenient Method for Preparations of 1-Acylimidazoles and Carboxamides by Using Novel Imidazolylsilane Derivatives
- Stereoselective Synthesis of trans-3, 4-Dihydropyran-2-ones by Phenoxide ion-catalyzed Tandem Michael Addition and Lactonization
- An Efficient Synthesis of 3, 4-Dihydropyran-2-one Derivatives by Lewis Base-catalyzed Tandem Michael Addition and Lactonization
- Lithium Alkoxide-promoted Michael Reaction between Silyl Enolates and α, β-Unsaturated Carbonyl Compounds