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POLYFLUOROALKYLATION OF CARBONYL COMPOUNDS BY POLYFLUOROALKYL ANIONS GENERATED FROM POLYFLUOROCARBOXAMIDES
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アクセス権 |
open access |
主題 |
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内容注記 |
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Abstract
en
Polyfluoroalkyl anions, generated by reduction of (polyfluoroalkanoyl)piperidines with Et3BHK, were used for the polyfluoroalkylation of carbonyl compounds. Trifluoromethylation of aromatic aldehydes proceeded in good yields, and that of aliphatic aldehydes afforded a moderate yield. In contrast, the yield was low when the reaction involved benzophenone. Pentafluoroethylation and octafluorobutylation of aldehydes were also carried out by using the corresponding (polyfluoroalkanoyl)piperidines, which were prepared from commercially available polyfluorocompounds. The (polyfluoroalkanoyDpiperidines were also prepared through polyfluorination, and were used in the polyfluoroalkylation of aldehydes.
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出版者 |
en
Pergamon-elsevier science ltd
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日付 |
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言語 |
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資源タイプ |
journal article |
出版タイプ |
SMUR |
資源識別子 |
HDL
http://hdl.handle.net/2115/54926
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関連 |
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DOI
https://doi.org/10.3987/COM-13-S(S)84
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収録誌情報 |
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Heterocycles
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巻88
号2
開始ページ1201
終了ページ1212
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ファイル |
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コンテンツ更新日時 |
2023-07-26 |