Thermal Aza-Bergman Cyclization of o-Alkynylaryl Isocyanides with Organic Diselenide, Ditelluride, and Iodine Leading to 2,4-Difunctionalized Quinolines
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
- 2011-07-15
著者
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Ogawa Akiya
Department Of Applied Chemistry Faculty Of Engineering Osaka Prefecture University
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MITAMURA Takenori
Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University
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Mitamura Takenori
Department Of Applied Chemistry Graduate School Of Engineering Osaka Prefecture University
関連論文
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- Rotaxane Synthesized by End-capping via Hydroruthenation of Axle Terminal Acetylene and Its Derivation to η^3-Allylruthenium Complex-containing Rotaxane
- Photoaccelerated Reductive Coupling of Acid Chlorides with Conjugate Dienes and Styrenes by Use of Neodymium Metal in N,N-Dimethylacetamide
- Carbonylation of Organic Halides with Carbon Monoxide Mediated by Samarium Diiodide. Improvement and Mechanistic Investigations
- Photoinduced Reduction of gem-Dichlorocyclopropanes with Sml_2 and Benzenethiol
- Highly Selective Addition of Organic Dichalcogenides to Carbon-Carbon Unsaturated Bonds
- Synthesis of 2-Halogenated Quinolines by Halide-Mediated Intramolecular Cyclization of o-Alkynylaryl Isocyanides
- Novel Photoinduced Reduction of Conjugate Dienes by the Combination of Benzenethiol and Diphenyl Diselenide
- Enhanced Reducing Ability by the Combination of SmI_2 and Sm Metal in the Reduction of Alkyl Halides
- Transition-Metal-Catalyzed Cyanochalcogenation of Alkynes with Chalcogenocyanates
- Highly Regioselective Double Hydrothiolation of Terminal Acetylenes with Thiols Catalyzed by Palladium Diacetate
- Vanadium-catalyzed Atmospheric Oxidation of Benzyl Alcohols Using Water as Solvent
- Copper-free Sonogashira Coupling Reaction Using a trans-Spanning 1,2-Bis(2-thienylethynyl)benzene Ligand
- Thermal Aza-Bergman Cyclization of o-Alkynylaryl Isocyanides with Organic Diselenide, Ditelluride, and Iodine Leading to 2,4-Difunctionalized Quinolines
- Highly Selective Addition of Organic Dichalcogenides to Carbon-Carbon Unsaturated Bonds
- Convenient synthesis of .BETA.-silyl ketones from .BETA.-stannyl enol silyl ethers via a (1,4) anionic rearrangement of silicon.
- Synthesis utilizing reducing ability of carbon monoxide. New methods for synthesis of N-substituted selenoamides.