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Conformational Analysis in Reversible Intramolecular [2+2] Photocycloaddition of Diphenylbicyclo[4.2.0]oct-3-ene-2,5-diones
http://hdl.handle.net/10173/1354
http://hdl.handle.net/10173/13541754ea4d-7ab1-4ca8-b4a1-da75056fd97f
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
27-39.pdf (295.3 kB)
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||
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| 公開日 | 2016-03-25 | |||||
| タイトル | ||||||
| タイトル | Conformational Analysis in Reversible Intramolecular [2+2] Photocycloaddition of Diphenylbicyclo[4.2.0]oct-3-ene-2,5-diones | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | journal article | |||||
| 著者 |
Asahara, Haruyasu
× Asahara, Haruyasu× Mochizuki, Eiko× Oshima, Takumi |
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| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | Irradiation of diphenylbicyclo[4.2.0]oct-3-ene-2,5-diones bearing variously substituted Me groups resulted in the reversible intramolecular [2+2] cycloaddition between the excited enedione C=C double bond and the facing endo-phenyl ring to exclusively give pentacyclotetradeca-10,12-diene-2,7-diones. The equilibrated product ratios were much dependent on the substitution pattern of the Megroups as well as the irradiated wavelength. The regiochemistry of these photoadditions was elucidated on the basis of the restricted conformation of the starting enediones. | |||||
| 書誌情報 |
Tetrahedron Letters 巻 47, 号 25, p. 7881-7884, 発行日 2006 |
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| DOI | ||||||
| 関連タイプ | isVersionOf | |||||
| 識別子タイプ | DOI | |||||
| 関連識別子 | 10.1016/j.tetlet.2006.09.013 | |||||
| 著者版フラグ | ||||||
| 出版タイプ | AM | |||||
| 出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
| 出版者 | ||||||
| 出版者 | Elsevier Ltd. | |||||
