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      Synthesis of trifluoromethyl-containing isoindolinones from tertiary enamides via a cascade radical addition and cyclization process†

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          A radical trifluoromethylation reaction of tertiary enamides was investigated and trifluoromethyl-containing isoindolinones were prepared under mild conditions. Using TMSCF 3 as a radical source, PhI(OAc) 2 as an oxidant and KHF 2 as an additive, tertiary enamides were converted to isoindolinones via a cascade addition and cyclization process in moderate to good yields.

          Abstract

          Radical trifluoromethylation and cyclization of tertiary enamides was developed and trifluoromethyl-containing isoindolinones were obtained in moderate to good yields.

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          Author and article information

          Journal
          RSC Adv
          RSC Adv
          RA
          RSCACL
          RSC Advances
          The Royal Society of Chemistry
          2046-2069
          3 July 2018
          27 June 2018
          3 July 2018
          : 8
          : 42
          : 23919-23923
          Affiliations
          [a] School of Chemical Science and Engineering, Shanghai Key Lab of Chemical Assessment and Substainability, Tongji University 1239 Siping Road Shanghai 200092 P. R. China yuhui@ 123456tongji.edu.cn +86 21 65981097 +86 21 65981097
          Author information
          https://orcid.org/0000-0002-5717-6635
          Article
          c8ra03696a
          10.1039/c8ra03696a
          9081866
          35540298
          31d49ca3-9324-409b-9444-5bf4e1c858ac
          This journal is © The Royal Society of Chemistry
          History
          : 30 April 2018
          : 15 June 2018
          Page count
          Pages: 5
          Funding
          Funded by: Tongji University, doi 10.13039/501100004204;
          Award ID: 20123231
          Categories
          Chemistry
          Custom metadata
          Paginated Article

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