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New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet–Hauser rearrangements
http://hdl.handle.net/10191/9512
http://hdl.handle.net/10191/9512097f0136-8f04-4a6e-a47d-5daaf00b57c9
名前 / ファイル | ライセンス | アクション |
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6_3673-3680aut.pdf (163.7 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2009-08-27 | |||||
タイトル | ||||||
タイトル | New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet–Hauser rearrangements | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet–Hauser rearrangements | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Tayama, Eiji
× Tayama, Eiji× Orihara, Kiwako× Kimura, Hiroshi |
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著者別名 | ||||||
識別子 | 7580 | |||||
識別子Scheme | WEKO | |||||
姓名 | 田山, 英治 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The Stevens rearrangement of N-allylic α-aryl amino acid-derived ammonium salts and the Sommelet–Hauser rearrangement of N-benzylic α-alkyl amino acid-derived ammonium salts are shown to proceed with remarkably high levels of diastereoselectivity. The methods presented in this work provide new routes to optically active α-quaternary α-aryl amino acid derivatives. | |||||
書誌情報 |
Organic and Biomolecular Chemistry en : Organic and Biomolecular Chemistry 巻 6, 号 20, p. 3673-3680, 発行日 2008-08 |
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出版者 | ||||||
出版者 | Royal Society Chemistry | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 14770520 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA1168650X | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | info:doi/10.1039/B811162F | |||||
著者版フラグ | ||||||
値 | author | |||||
異版である | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | URI | |||||
関連識別子 | http://www.rsc.org/Publishing/Journals/OB/article.asp?doi=b811162f |