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3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones
http://hdl.handle.net/10069/37368
http://hdl.handle.net/10069/37368e520d9ff-3657-448e-8494-9401db17f2ba
名前 / ファイル | ライセンス | アクション |
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OCF3_1661.pdf (442.1 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2018-01-01 | |||||
タイトル | ||||||
タイトル | 3,3-Dibromo-2-trifluoromethyl acrylic acid ethyl ester: a versatile platform for the stereoselective preparation of functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones | |||||
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 |
Mizuta, Satoshi
× Mizuta, Satoshi× Otaki, Hiroki× Kitamura, Kanami× Nishi, Kodai× Watanabe, Ken× Makau, Juliann Nzembi× Hashimoto, Ryo× Usui, Toshiya× Chiba, Kenya |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | We herein describe a method for synthetic routes to multi-functionalized-α-trifluoromethyl α,β-unsaturated lactones and trifluoromethyl pyrazolinones. This involves a tandem stereoselective functionalization of 3,3-dibromo-2-trifluoromethyl acrylic acid ethyl ester and intramolecular cyclization reaction to afford precursors for a Suzuki-Miyaura cross-coupling reaction with arylboronic acids. | |||||
書誌情報 |
Organic Chemistry Frontiers 巻 3, 号 12, p. 1661-1667, 発行日 2016-12 |
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出版者 | ||||||
出版者 | Royal Society of Chemistry | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 20524129 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1039/C6QO00360E | |||||
権利 | ||||||
権利情報 | c the Partner Organisations 2016. | |||||
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 | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | Organic Chemistry Frontiers, 3(12), pp.1661-1667; 2016 |