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Mechanistic evidence for the remote π-aryl participation in acidcatalyzed ring opening of homobenzoquinone epoxides
http://hdl.handle.net/10173/1352
http://hdl.handle.net/10173/1352a288e29d-b235-49b3-912a-fdd672343e20
名前 / ファイル | ライセンス | アクション |
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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 | Mechanistic evidence for the remote π-aryl participation in acidcatalyzed ring opening of homobenzoquinone epoxides | |||||
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 |
Oshima, Takumi
× Oshima, Takumi× Asahara, Haruyasu× Koizumi, Takuya× Miyamoto, Saki |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The acid-induced reaction of bis(p-chlorophenyl)homobenzoquinone epoxide gave the dual ipso/ortho intramolecular SE2-Ar products associated with the π-aryl participated oxirane ring opening, whereas bis(p-tolyl)- and diphenyl-substituted homologues provided only the ortho products. | |||||
書誌情報 |
Chemical Communications 巻 15, p. 1804-1806, 発行日 2008 |
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DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1039/B719663F | |||||
権利(URI) | ||||||
権利情報 | http://pubs.rsc.org/en/content/articlelanding/2008/cc/b719663f#!divAbstract | http://pubs.rsc.org/en/content/articlelanding/2008/cc/b719663f#!divAbstract | |||||
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 | Royal Society of Chemistry |