Tetrahedron Letters, Год журнала: 2024, Номер 154, С. 155370 - 155370
Опубликована: Ноя. 17, 2024
Язык: Английский
Tetrahedron Letters, Год журнала: 2024, Номер 154, С. 155370 - 155370
Опубликована: Ноя. 17, 2024
Язык: Английский
ACS Catalysis, Год журнала: 2024, Номер 14(21), С. 15879 - 15907
Опубликована: Окт. 11, 2024
Partially fluorinated alkyl groups other than methyl are increasingly playing crucial roles in the development of drugs with diverse biological activities, thus creating an innovative chemical space within organofluorine chemistry. For studies structure–activity relationships, late-stage modification such or substituents into substrates that bear activity is essential. This perspective will study catalytic protocols for direct introduction partially monofluoroalkylated (−CHFR, –CH2CH2F), difluoroalkylated (−CF2Me, –CH2CF2H), trifluoroalkylated (−CHR(CF3), –CH2CF3, –CH2CH2CF3, –CH(Me)CF3, –C(Me)2CF3), and pentafluoropropylated (−CH2C2F5) onto (hetero)aromatic compounds, double bonds, isonitriles, halides, N, O, S atoms.
Язык: Английский
Процитировано
2Tetrahedron Letters, Год журнала: 2024, Номер 154, С. 155370 - 155370
Опубликована: Ноя. 17, 2024
Язык: Английский
Процитировано
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