4.7 Article

Regio- and Stereoselective Allylic Trifluoronnethylation and Fluorination using CuCF3 and CuF Reagents

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JOURNAL OF ORGANIC CHEMISTRY
卷 78, 期 14, 页码 7330-7336

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AMER CHEMICAL SOC
DOI: 10.1021/jo4010074

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  1. Swedish Research Council (VR)
  2. Knut och Alice Wallenbergs Foundation via the Center of Molecular Catalysis at Stockholm University (CMCSU)

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Copper-mediated trifluoromethylation of allylic chlorides and trifluoroacetates was performed using a convenient Cu-CF3 reagent. The reaction is suitable for selective synthesis of allyl trifluoromethyl species. Mechanistic studies indicate that the reaction proceeds via a nucleophilic substitution mechanism involving allyl copper intermediates. The analogous Cu-F reagent was suitable for fluorination of allyl chlorides. Stereodefined cyclic substrates reacted regio- and stereoselectively.

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