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In the case of the reaction with the 1-azulenyl methyl sulfide (12), 1,1\u0027-biazulene derivative 13 was obtained under the similar reaction conditions. The first synthesis of unsymmetrical 1,3-di(pyridyl)azulene derivative was also established via our new preparation method following the electrophilic pyriclinylation using the reaction with pyridine in the presence of Tf(2)O. (c) 2010 Elsevier Ltd. 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Synthesis of 1-(pyridyl, quinolyl, and isoquinolyl)azulenes by Reissert-Henze type reaction
http://hdl.handle.net/10091/16093
9570f5b5-7745-4e7b-83de-7b50f01bd418
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 | 2012-11-26 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Synthesis of 1-(pyridyl, quinolyl, and isoquinolyl)azulenes by Reissert-Henze type reaction | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Azulene | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Heterocycle | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Electrophilic arylation | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Shoji, Taku
× Shoji, Taku× Okada, Kazuyuki× Ito, Shunji× Toyota, Kozo× Morita, Noboru |
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信州大学研究者総覧へのリンク | ||||||
氏名 | Shoji, Taku | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.gmShOakh.html | |||||
出版者 | ||||||
出版者 | PERGAMON-ELSEVIER SCIENCE LTD | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | TETRAHEDRON LETTERS. 51(39):5127-5130 (2010) | |||||
書誌情報 |
TETRAHEDRON LETTERS 巻 51, 号 39, p. 5127-5130, 発行日 2010-09-29 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Azulene derivatives reacted with N-oxide of several heterocycles in the presence of trifluoromethanesultonic anhydride (Tf(2)O) to afford 1-(pyridyl, quinolyl, and isoquinolyl)azulenes in good yield, respectively. In the case of the reaction with the 1-azulenyl methyl sulfide (12), 1,1'-biazulene derivative 13 was obtained under the similar reaction conditions. The first synthesis of unsymmetrical 1,3-di(pyridyl)azulene derivative was also established via our new preparation method following the electrophilic pyriclinylation using the reaction with pyridine in the presence of Tf(2)O. | |||||
資源タイプ(コンテンツの種類) | ||||||
内容記述タイプ | Other | |||||
内容記述 | Article | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0040-4039 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00861801 | |||||
DOI | ||||||
関連識別子 | ||||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.1016/j.tetlet.2010.07.090 | |||||
関連名称 | ||||||
関連名称 | 10.1016/j.tetlet.2010.07.090 | |||||
出版タイプ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
WoS | ||||||
表示名 | Web of Science | |||||
URL | http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=ShinshuUniv&SrcApp=ShinshuUniv&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000282150800008 |