Development of Highly Selective Organic Reactions Catalyzed by Designed Amine Organocatalysts
スポンサーリンク
概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 2010-12-15
著者
-
Maruoka Keiji
Department Applied Chemistry Nagoya University
-
Kano Taichi
Department Of Chemistry Graduate School Of Science Kyoto University
関連論文
- Evaluation of the Relationship between the Catalyst Structure and Regio- as well as Stereoselectivity in the Chiral Ammonium Bifluoride-Catalyzed Asymmetric Addition of Silyl Nitronates to α, β-Unsaturated Aldehydes
- Organoaluminum-Promoted Cyclization of Olefinic Epoxides. A New and Stereoselective Approach to Cyclohexane Frameworks
- SLB11 NEW APPROACH FOR NATURAL PRODUCT SYNTHESIS USING MAIN GROUP ORGANOMETALLIC REAGENTS
- 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
- Direct Asymmetric Aminoxylation Reaction Catalyzed by Axially Chiral Amino Acids
- A Facile Workup-Free Catalytic Rearrangement of Epoxides on Immobilized Organoaluminum Columns
- Phase-transfer-catalyzed Asymmetric Alkylation with Epoxy Triflates as Alkylating Agents : Highly Stereoselective Synthesis of γ,δ-Epoxy-α-amino Acids
- Catalytic asymmetric synthesis of α-amino acid derivatives and peptides using chiral phase-transfer catalysts
- Development of Highly Selective Organic Reactions Catalyzed by Designed Amine Organocatalysts
- Design of Sophisticated Bidentate Lewis Acids and Organocatalysts for Fine Organic Synthesis
- Catalytic Asymmetric Synthesis of Isoxazoline-N-oxides through Conjugate Addition-Cyclization under Phase-Transfer Conditions
- Selective separation of structurally or electronically similar ethers with MAD.
- Conjugate reduction of .ALPHA.,.BETA.-unsaturated ketones with amphiphilic reaction system.