Bromination of Cyclic 1,3-Diketone Monoenolates with N-Bromosuccinimide. III.
スポンサーリンク
概要
- 論文の詳細を見る
The position of substituted bromine in the product obtained by bromination with N-bromosuccinimide of 1,3-cyclohexanedione 3-monoenolates having two alkyl substituents at the 5-position was established as 6,probably in axial conformation.
- 公益社団法人日本薬学会の論文
- 1957-12-20
著者
関連論文
- Antibacterial Activity of Compounds possessing a Tricarbonylmethane Group. XI. Synthesis of a Compound having Structure analogous to A-Ring of Tetracycline.
- Bromination of Cyclic 1,3-Diketone Monoenolates with N-Bromosuccinimide. III.
- Bromination of Cyclic 1,3-Diketone Monoenolates with N-Bromosuccinimide. II.
- Bromination of Cyclic 1,3-Diketone Monoenolates with N-Bromosuccinimide. I.
- Antibacterial Activity of Compounds Possessing a Tricarbonylmethane Group. X. : Observations on the Acetylation of 4-Hydroxycoumarin and Synthesis of 3-(α-Aminophenylacetyl)-4-hydroxycoumarins.
- Antibacterial Properties of Compounds Containing the Tricarbonylmethane Group. IX. : Effects of Nitrogenous Radicals in the Side-chains of 3-Acyl-4-hydroxycoumarins and its Derivatives.