| ID | 62010 |
| FullText URL | |
| Author |
Nishihara, Yasushi
Research Institute for Interdisciplinary Science, Okayama University
ORCID
Kaken ID
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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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| Abstract | 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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| Keywords | C-F bond activation
decarbonylation
thioetherification
acyl fluorides
sulfides
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| Note | This is an Accepted Manuscript of an article published by Georg Thieme Verlag KG
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| Published Date | 2021-4-16
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| Publication Title |
Synthesis
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| Volume | volume53
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| Issue | issue17
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| Publisher | Georg Thieme Verlag KG
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| Start Page | 3045
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| End Page | 3050
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| ISSN | 0039-7881
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| NCID | AA00855740
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| Content Type |
Journal Article
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| language |
English
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| OAI-PMH Set |
岡山大学
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| Copyright Holders | © 2021. Thieme.
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| File Version | author
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| DOI | |
| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.1055/a-1484-6216
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