Stereospecific Synthesis of cis- and trans-2,3-Epoxycycloheptanol
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概要
- 論文の詳細を見る
cis- and trans-2,3-Epoxycycloheptanols were prepared stereospecifically from cyclohept-2-en-1-ol (1). Oxidation of 1 with tert-butyl hydroperoxide in the presence of a molybdenum catalyst gave the cis isomer (2) in high yield. The trans isomer (3) was obtained via the bromohydrin (4). The structure of 4 is discussed.
- 社団法人日本薬学会の論文
- 1980-03-25
著者
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尾崎 裕
城西大学薬学部
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尾崎 裕
Faculty Of Pharmaceutical Sciences Osaka University
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金 相元
城西大学薬学部
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金 相元
Faculty of Pharmaceutical Sciences, Josai University
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長尾 恵四郎
Faculty of Pharmaceutical Sciences, Josai University
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吉村 磯孝
Faculty of Pharmaceutical Sciences, Josai University
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金 相元
Faculty Of Pharmaceutical Sciences Josai University
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Ozaki Y
Division Of Pharmacognosy And Phytochemistry National Institute Of Health Sciences
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Ozaki Y
National Inst. Health Sci. Tokyo Jpn
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吉村 磯孝
Faculty Of Pharmaceutical Sciences Josai University
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長尾 恵四郎
Faculty Of Pharmaceutical Sciences Josai University
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