Silver-catalyzed Vinylic C–F Bond Activation: Synthesis of 2-Fluoroindoles from β,β-Difluoro-<i>o</i>-sulfonamidostyrenes
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- Fujita Takeshi
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
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- Watabe Yota
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
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- Yamashita Shigeyuki
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
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- Tanabe Hiroyuki
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
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- Nojima Tomoya
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
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- Ichikawa Junji
- Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba
説明
An electrophilic 5-endo-trig cyclization of β,β-difluoro-o-sulfonamidostyrenes was performed in 1,1,1,3,3,3-hexafluoropropan-2-ol using a Ag(I) catalyst and N,O-bis(trimethylsilyl)acetamide. In this process, vinylic C–F bond activation was achieved via silver-catalyzed β-fluorine elimination, accompanied by C–N bond formation, which led to the synthesis of 2-fluoroindoles.
収録刊行物
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- Chemistry Letters
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Chemistry Letters 45 (8), 964-966, 2016
公益社団法人 日本化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679564445824
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- NII論文ID
- 130005254491
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- ISSN
- 13480715
- 03667022
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可