| ID | 62010 |
| フルテキストURL | |
| 著者 |
Nishihara, Yasushi
Research Institute for Interdisciplinary Science, Okayama University
ORCID
Kaken ID
publons
researchmap
You, Jingwen
Graduate School of Natural Science and Technology, Okayama University
Chen, Qiang
Graduate School of Natural Science and Technology, Okayama University
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| 抄録 | Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulfides can be obtained in good to excellent yields. This protocol provides the formation of diverse carbon–sulfur bonds via a highly efficient decarbonylative process.
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| キーワード | C-F bond activation
decarbonylation
thioetherification
acyl fluorides
sulfides
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| 備考 | This is an Accepted Manuscript of an article published by Georg Thieme Verlag KG
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| 発行日 | 2021-4-16
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| 出版物タイトル |
Synthesis
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| 巻 | 53巻
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| 号 | 17号
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| 出版者 | Georg Thieme Verlag KG
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| 開始ページ | 3045
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| 終了ページ | 3050
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| ISSN | 0039-7881
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| NCID | AA00855740
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| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
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| OAI-PMH Set |
岡山大学
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| 著作権者 | © 2021. Thieme.
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| 論文のバージョン | author
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| DOI | |
| Web of Science KeyUT | |
| 関連URL | isVersionOf https://doi.org/10.1055/a-1484-6216
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