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  1. 050 理学部
  2. 10 学術雑誌論文
  3. 10 査読済論文
  1. 0 資料タイプ別
  2. 01 学術雑誌論文

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/10191/9512
097f0136-8f04-4a6e-a47d-5daaf00b57c9
名前 / ファイル ライセンス アクション
6_3673-3680aut.pdf 6_3673-3680aut.pdf (163.7 kB)
Item type 学術雑誌論文 / Journal Article(1)
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

WEKO 7577

Tayama, Eiji

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Orihara, Kiwako

× Orihara, Kiwako

WEKO 7578

Orihara, Kiwako

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Kimura, Hiroshi

× Kimura, Hiroshi

WEKO 7579

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
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
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