From S-Fluoroalkylation to Fluoroalkylation–Thiolation: Difunctionalization of Alkenes with Fluoroalkyl Phenyl Sulfones and Thiophenols Enabled by Photoredox Copper Catalysis Научная публикация
Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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Вых. Данные | Год: 2025, Том: 27, Номер: 8, Страницы: 1884–1888 Страниц : DOI: 10.1021/acs.orglett.5c00102 | ||||||
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Реферат:
Molecules containing fluoroalkyl and arylthio groups play a pivotal role in pharmaceutical and agrochemical development. The simultaneous introduction of these functional groups through the 1,2-difunctionalization of alkenes is an efficient strategy. Fluoroalkyl phenyl sulfones serve as accessible fluoroalkyl radical precursors; however, their tendency to interact with thiophenol via the electron donor–acceptor interaction mechanism can impede the desired transformation. Through meticulous selection of solvent and base, we successfully utilized copper catalysis to facilitate an alkene-involved three-component reaction. Our work unveils a photoredox copper-catalyzed fluoroalkylation–thiolation of alkenes using various fluoroalkyl phenyl sulfones (such as perfluoroethyl, tetrafluoroethyl, trifluoromethyl, difluoromethyl, difluoroalkyl, and difluorobenzyl). The efficacy of this approach is exemplified by the synthesis of Kengreal derivatives.
Библиографическая ссылка:
Xiao L.
, Wei Z.
, Ni C.
, Dilman A.D.
, Hu J.
From S-Fluoroalkylation to Fluoroalkylation–Thiolation: Difunctionalization of Alkenes with Fluoroalkyl Phenyl Sulfones and Thiophenols Enabled by Photoredox Copper Catalysis
Organic Letters. 2025. V.27. N8. P.1884–1888. DOI: 10.1021/acs.orglett.5c00102 WOS OpenAlex
From S-Fluoroalkylation to Fluoroalkylation–Thiolation: Difunctionalization of Alkenes with Fluoroalkyl Phenyl Sulfones and Thiophenols Enabled by Photoredox Copper Catalysis
Organic Letters. 2025. V.27. N8. P.1884–1888. DOI: 10.1021/acs.orglett.5c00102 WOS OpenAlex
Идентификаторы БД:
Web of science: | WOS:001423590000001 |
OpenAlex: | W4407652696 |
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