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Synthesis of Spiro[2-cyclopentene-1,3’-imidazo[1,2-a]pyridine] Derivatives and Their Interesting Behavior in 1H-NMR Spectra in Deuteriochloroform
http://hdl.handle.net/10091/10742
http://hdl.handle.net/10091/107427201c5c1-b733-4fe8-8d24-f9feb834d998
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 | 2010-10-27 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Synthesis of Spiro[2-cyclopentene-1,3’-imidazo[1,2-a]pyridine] Derivatives and Their Interesting Behavior in 1H-NMR Spectra in Deuteriochloroform | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Imidazo[1,2-a]pyridine | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Spiro[2-cyclopentene-1,3’-imidazo[1,2-a]pyridine] | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Synthesis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Concentration Dependency of Proton Signal | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | X-Ray Analysis | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Abe, Takashi
× Abe, Takashi× Kakehi, Akikazu× Suga, Hiroyuki× Okumura, Yukihisa× Itoh, Kennosuke |
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信州大学研究者総覧へのリンク | ||||||
氏名 | Suga, Hiroyuki | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.HmShyVfp.html | |||||
信州大学研究者総覧へのリンク | ||||||
氏名 | Okumura, Yukihisa | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.gNDVgpAF.html | |||||
出版者 | ||||||
出版者 | The Japan Institute of Heterocyclic Chemistry | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | HETEROCYCLES. 81(9):2075-2086 (2010) | |||||
書誌情報 |
HETEROCYCLES 巻 81, 号 9, p. 2075-2086, 発行日 2010-09-01 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Ethyl 2',3'-dihydro-2-methylthio-2',4-dioxospiro[2-cyclopentene-1,3'-imidazo[1,2-a]pyridine]-3-carboxylates were synthesized from the reactions of 3-[bis(methylthio)methylene]-2(3H)-imidazo[1,2-a]pyridinones with ethyl 4-chloroacetoacetate in the presence of a base. The 2-methylthio group in these Spiro compounds was easily replaced with some primary and secondary amines to afford the corresponding 2-amino derivatives. Very interestingly, the proton signals of these Spiro compounds in the H-1-NMR spectra in deuteriochloroform (CDCl3) changed with an increase in the sample concentration, and the analysis for the magnitude and the direction of each proton shift disclosed the conformational change of the cyclopentenone moiety in this molecule. | |||||
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 | 0385-5414 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00663739 | |||||
他の資源との関係:URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | http://www.heterocycles.jp/ | |||||
関連名称 | http://www.heterocycles.jp/ | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.3987/COM-10-11985 | |||||
関連名称 | 10.3987/COM-10-11985 | |||||
権利 | ||||||
権利情報 | Copyright© 2010 The Japan Institute of Heterocyclic Chemistry | |||||
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=000282865300005 |