Rearrangement of 11-Hydroxy-11-(2-naphthyl)-3,4:8,9-dibenzobicyclo [4.4.1]undeca-3,8-diene-2,2,5,5,7,7,10,10-d_8
スポンサーリンク
概要
- 論文の詳細を見る
The preparation of a novel deuterated [3.3]orthocyclophane-alcohol is described. The rearrangement of the orthocyclophane alcohol leads to a dibenzo-annelated bromomethyldecaline. The deuterium labels provide a good indication of the mechanism that is underlying this reaction.
- 九州大学の論文
- 2000-07-01
著者
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Sawada T
Institute Of Advanced Material Study Kyushu University
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Mataka S
Kyushu Univ. Kasuga
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Mataka Shuntaro
Department Of Molecular Science And Technology Graduate School Of Engineering Sciences Kyushu Univer
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Mataka Shuntaro
Institute Of Advanced Material Kyushu University
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Mataka Shuntaro
Institute Of Advanced Material Study Kyushu University
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Yonemitsu Tadashi
Department of Industrial Chemistry, Faculty of Engineering, Kyushu Sangyo University
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Yonemitsu T
Department Of Industrial Chemistry Faculty Of Engineering Kyushu Sangyo University
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THIEMANN Thies
Institute of Advanced Material Study, Kyushu University
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ISOBE Shin-ichiro
Graduate School of Engineering Sciences, Kyushu University
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Isobe Shin-ichiro
Department Of Molecular Science And Technology Graduate School Of Engineering Sciences Kyushu Univer
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Thiemann T
Institute Of Advanced Material Study Kyushu University
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Yonemitsu Tadashi
Department Of Industrial Chemistry Faculty Of Engineering Kyushu Sangyo University
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