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Iron-catalysed reductive coupling for the synthesis of polyfluorinated compounds.
Guan, Yu-Qiu; Wang, Tian-Zhang; Qiao, Jia-Fan; Chen, Zhangpei; Bai, Zhushuang; Liang, Yu-Feng.
Afiliação
  • Guan YQ; Center for Molecular Science and Engineering, College of Sciences, Northeastern University, Shenyang 110819, China. chenzhangpei@mail.neu.edu.cn.
  • Wang TZ; School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. yfliang@sdu.edu.cn.
  • Qiao JF; School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. yfliang@sdu.edu.cn.
  • Chen Z; School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. yfliang@sdu.edu.cn.
  • Bai Z; Center for Molecular Science and Engineering, College of Sciences, Northeastern University, Shenyang 110819, China. chenzhangpei@mail.neu.edu.cn.
  • Liang YF; School of Pharmacy and Pharmaceutical Science & Institute of Materia Medica, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250117, China. baizhushuang@163.com.
Chem Commun (Camb) ; 58(100): 13915-13918, 2022 Dec 15.
Article em En | MEDLINE | ID: mdl-36445240
Herein we reported the use of Earth-abundant iron as the catalytic metal in the presence of Mn to induce difluorobromoacetates to form carbon radicals, which reacted with trifluoromethyl olefins followed by ß-F elimination to generate the corresponding gem-difluoroolefins. The cross-electrophile coupling displayed excellent functional group tolerance and broad substrate scope under mild reductive conditions, affording a large number of polyfluorinated compounds, which could be further transformed to other valuable molecules.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alcenos / Ferro Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alcenos / Ferro Idioma: En Ano de publicação: 2022 Tipo de documento: Article