Asymmetric Transfomation. II. : Racemization Reaction of 1,4-Benzodiazepinoxazole Derivative
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概要
- 論文の詳細を見る
Optically active crystals of 10-bromo-11b-(2-fluorophenyl)-2,3,7,11b-tetrahydrooxazolo-[3,2-d][1,4]denzodiazepin-6(5H)-one were obtained by preferential crystallization; they were sometimes levorotary and sometimes dextrorotatory. This phenomenon was proved to be an example of second-order asymmetric transformation between enantiomers. The rapid recemization reaction, which was essential for asymmetric transformation, was observed in methanol. The decrease of optical rotation obeyed good pseudo first-order kinetics and the half-lives of the racemization in methanol were estimated to be about 21 s at 30℃, 37s at 20℃ and 70s at 10℃. The mechanism and factors which affect the rate of the recemization are discussed.
- 公益社団法人日本薬学会の論文
- 1988-10-25
著者
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岡田 泰
Process Development Laboratories Sankyo Co. Ltd.
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竹林 潔矩
Process Development Laboratories, Sankyo Co., Ltd.,
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竹林 潔矩
Process Development Laboratories Sankyo Co. Ltd.
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- Asymmetric Transformation. III. : Crystal Properties and Structures of a 1,4-Benzodiazepinooxazole Derivative
- Asymmetric Transfomation. II. : Racemization Reaction of 1,4-Benzodiazepinoxazole Derivative
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