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Electrochemical synthesis of β-difluoromethylamide compounds by N-benzenesulfonylacrylamide with difluorine reagents
Chemical Communications ( IF 4.3 ) Pub Date : 2024-06-28 , DOI: 10.1039/d4cc02543a
Zhi-Long Lei 1 , Zong-Cang Ding 2 , Shu-Hui Li 1 , Fei-Hu Cui 1 , Hai-Tao Tang 1 , Ying-Ming Pan 1
Affiliation  

A mild and efficient electrochemical method for radical addition, cyclization, and migration reaction was described in this work. A difluoromethyl radical was produced by anodizing CF2HSO2Na. The resulting product was then added to olefin, underwent Smiles cyclization, and migrated to form β-difluoromethamide compounds after the release of SO2. The process was free from metals and catalysts, gram-grade, and resistant to a variety of electron-rich substrates.

中文翻译:


N-苯磺酰丙烯酰胺与二氟试剂电化学合成β-二氟甲酰胺类化合物



这项工作描述了一种温和有效的自由基加成、环化和迁移反应的电化学方法。通过阳极氧化 CF 2 HSO 2 Na 产生二氟甲基自由基。然后将所得产物加入到烯烃中,进行Smiles环化,并在释放SO 2 后迁移形成β-二氟甲酰胺化合物。该工艺不含金属和催化剂,是克级的,并且对各种富电子底物具有耐受性。
更新日期:2024-07-03
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