書誌事項
- タイトル別名
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- The Reactivities of the Aromatic Amido- and Oxy-Claisen Rearrangements -The Correlation with the Bond Localization Energy-
抄録
The amido-Claisen rearrangement of N-allyl-N-mesyl derivatives of aniline, 1- and 2- naphthylamines, and 2-, 3- and 9-aminophenanthrenes was kinetically investigated. A good linear relationship between In K and the bond localization energy (BLE) was observed in the rearrangement. In the corresponding oxy-Claisen rearrangement, the kinetical data described in literature were similarly correlated with BLE. These results may demonstrate that the reactivities of these aromatic Claisen rearrangements depend on the difference of the resonance energy between the reactant and the transition state.<BR>The rearrangement of the N-naphthylamides and N-phenanthrylamides, as well as the corresponding oxy-Claisen rearrangement, gave experimentally no position isomers. The pro- babilities of the isomer formation were calculated from the correlated expressions.
収録刊行物
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- 日本化学会誌(化学と工業化学)
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日本化学会誌(化学と工業化学) 1978 (4), 571-577, 1978
公益社団法人 日本化学会
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キーワード
詳細情報 詳細情報について
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- CRID
- 1390282679393493120
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- NII論文ID
- 130004156140
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- ISSN
- 21850925
- 03694577
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可