Stereochemistry of the Intramolecular Substitution of Phnylselenonyl Group by Nitrogen Atom in Amide. Inversion of Configuration
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概要
- 論文の詳細を見る
- 1992-10-05
著者
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Fuji Hidekiyo
Institute For Chemical Research Kyoto University
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TOSHIMITSU Akio
Institute for Chemical Research, Kyoto University
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Toshimitsu Akio
Institute For Chemical Research Kyoto University
関連論文
- Stereochemistry of the Intramolecular Substitution of Phnylselenonyl Group by Nitrogen Atom in Amide. Inversion of Configuration
- Nucleophilic Addition of a Divalent Silicon Species Bearing the 8-Dimethylamino-1-naphthyl Group to Diphenylacetylenes to Form the 1-Amino-1-silaphenalene Skeleton
- Trimerization of a Divalent Silicon Species Bearing the 8-Dimethylamino-1-naphthyl Group Accompanied by the Migration of Methyl and Dimethylamino Groups
- Wurtz - type Coupling Reaction of Pseudo - pentacoordinate Halodisilanes Using Magnesium : Enhanced Reactivity of the Silicon - Halogen Bond by Intramolecular Amine - Coordination to Silicon
- Intramolecular Cyclization Reaction via a Sterically Protected Episelenonium Ion Intermediate
- Enhanced Leaving Ability of Methoxy Group and Retarded Deprotonation on the Carbon Atom Linked to the 1-Position of 8-Phosphino- or 8-Amino-naphthalene
- Asymmetric Carbon-Carbon Bond Formations by the Reaction of "Chiral Episulfonium Ions" with Enol Silyl Ethers
- Chlorination of acetylenes with sulfuryl chloride.
- The reaction of alkyl halides with mercury(II) and potassium thioacetates and selenocyanates.
- Selenocyanatodethallation in Organothallium(III) Compounds
- Amidoselenation of Olefins Using p-Toluenesulfonamide as a Nitrogen Nucleophile.
- Oxidation of olefins with thallium(III) acetate in diols.