Selective Conjugate Alkylation of Alkyllithium Nucleophiles to α, β, γ, δ-Unsaturated aldehydes with functionalized Lewis Acid Receptors
スポンサーリンク
概要
- 論文の詳細を見る
- 1998-05-05
著者
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Ooi Takashi
Department Of Applied Chemistry Graduate School Of Engineering Nagoya University
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Kondo Yuichiro
Department Of Chemistry Graduate School Of Science Hokkaido University
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Maruoka Keiji
Department Applied Chemistry Nagoya University
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KON-I Kana
Department of Chemistry, Graduate School of Science, Hokkaido University
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Kon-i Kana
Department Of Chemistry Graduate School Of Science Hokkaido University
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Ooi Takashi
Department of Chemistry, Graduate School of Science, Hokkaido University
関連論文
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- Organoaluminum-Promoted Cyclization of Olefinic Epoxides. A New and Stereoselective Approach to Cyclohexane Frameworks
- Development of P-Spiro Chiral Aminophosphonium Salts as a New Class of Versatile Organic Molecular Catalyst
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- A Convergent, Homochiral Bis (amino alcohol) for Obtaining High Enantioselectivity in the Addition of Diethylzinc to Aldehydes
- Organoaliminum-Promoted Rearrangement of Epoxysilanes to α-Silylaldehydes
- Selective Conjugate Alkylation of Alkyllithium Nucleophiles to α, β, γ, δ-Unsaturated aldehydes with functionalized Lewis Acid Receptors
- Facile and Selective Alkylation of 3,3,3-Trifluoropropene Oxide (TFPO) with Organoaluminum Reagents via Pentacoordinate Trialkylaluminum Complexes
- Development of a Practical Synthetic Method for N-tert-Butoxycarbonyl α-Ketimino Esters
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- A Facile Workup-Free Catalytic Rearrangement of Epoxides on Immobilized Organoaluminum Columns
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- Development of Highly Selective Organic Reactions Catalyzed by Designed Amine Organocatalysts
- Design of Sophisticated Bidentate Lewis Acids and Organocatalysts for Fine Organic Synthesis
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- Selective separation of structurally or electronically similar ethers with MAD.
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