Yamane Yoshinobu | 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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YAMANE Yoshinobu
Center for Basic Research, The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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Yamane Yoshinobu
Center For Basic Research The Kitasato Institute
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Tozawa Takashi
Center For Basic Research The Kitasato Institute
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Minowa Tomofumi
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
Center for Basic Research, The Kitasato Institute
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NAGAO Hitoshi
Center for Basic Research, The Kitasato Institute
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Nagao Hitoshi
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 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
- Asymmetric Trifluoromethylation of Ketones with (Trifluoromethyl)trimethylsilane Catalyzed by Chiral Quaternary Ammonium Phenoxides
- Effective Synthesis of 5-Substituted Butenolide Derivatives by Using Cinchonidine-derived Quaternary Ammonium Phenoxide Catalyst
- Efficient synthesis of substituted 3-amino-3,4-dihydropyran-2-ones diastereo and enantioselective tandem Michael addition and lactonization between α,β-unsaturated ketones and glycine-derived silyl enolates using a chiral quaternary ammonium phenoxide
- Diastereo- and Enantioselective Synthesis of 3-Amino-3,4-dihydropyran-2-ones by Tandem Michael Addition and Lactonization Using a Chiral Quaternary Ammonium Phenoxide
- Diastereo- and Enantioselective Tandem Michael Addition and Lactonization Catalyzed by Chiral Quaternary Ammonium Phenoxide : Stereoselective Synthesis of the Two Enantiomers by Using a Single Chiral Source