Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
Organic Letters, Год журнала: 2025, Номер 27(4), С. 1072 - 1077
Опубликована: Янв. 18, 2025
A Cu(I) photoredox-enabled reaction that selectively incorporates a difluoroalkyl group into N-aryl glycine derivatives has been established. Using bench-stable [Ph3PCF2H]+Br- salt, the -CF2H could be installed either directly on α-carbon of backbone or in three-component fashion using an alkene as bridge. series have evaluated, providing access to diverse unnatural amino esters and dipeptides with -CHF2 unit. The studies compatibility other perfluorinated alkyl radical precursors showed selectivity direct α-coupling is closely associated electronic property radical, while works well most cases.
Язык: Английский
Процитировано
1ACS Catalysis, Год журнала: 2025, Номер unknown, С. 6826 - 6851
Опубликована: Апрель 14, 2025
Язык: Английский
Процитировано
0Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(16), С. 3405 - 3416
Опубликована: Июнь 12, 2024
Abstract The enantioselective introduction of gem ‐difluorinated carbonyl (i. e. α , ‐difluoro carbonyl) moieties into organic structures is a synthetically valuable but highly challenging approach. During the past decades, continuous efforts have been made for developments synthetic strategies constructing C( sp 3 )−CF 2 COR chiral centers with high levels enantioselectivities. This review summarizes and discusses recent advance in construction moieties, which are organized according to reaction categories.
Язык: Английский
Процитировано
2Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
Процитировано
0