Wagner-Meerwein Rearrangement of Allylbenzene Derivatives. I. Bromination of Safrole
スポンサーリンク
概要
- 論文の詳細を見る
The reaction of safrole (I) with bromine (II) was examined giving different results from the literature, i.e., 2,3-dibromo-1-(3', 4'-methylenedioxyphenyl) propane (III), 1,3-dibromo-2-(3', 4'-methylenedioxyphenyl) propane (V) and their bromo-substituted derivatives (IV and VI) were obtained. The formation of rearranged adducts (V and VI) suggests that Wagner-Meerwein rearrangement occured during this addition. The relationship between the reaction conditions and the ratio of the products was investigated.
- 公益社団法人日本薬学会の論文
- 1975-03-25
著者
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大槻 一夫
Faculty Of Pharmaceutical Sciences Kinki University
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入野 妙子
Faculty of Pharmacy, Kinki University
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入野 妙子
Faculty Of Pharmaceutical Sciences Kinki University
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- Reaction of Propenylbenzene Derivatives and Their Analogs. I. Reaction of N, N-Dibromobenzenesulfonamide with Propenylbenzene Derivatives
- Reaction of N-Haloamide. XXIII. Reaction of N, N-Dibromobenzenesulfonamide with Isosafrole
- Wagner-Meerwein Rearrangement of Allylbenzene Derivatives. I. Bromination of Safrole
- Reaction of N-Haloamide. XXII. Reaction of N, N-Dibromobenzenesulfonamide with Safrole
- Isomerization between trans-2-Benzenesulfonamido-3-bromotetrahydropyran and Its Isomer
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