ARTIKEL

Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis

04.03.2024
Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis

Photocatalytic hydro-difluoromethylaton of unactivated alkenes has been developed using a commercially available difluoromethylating reagent (CF2HSO2Na). This methodology tolerates a variety of functional groups and allows late-stage modification of various alkenes derived from pharmaceutically relevant drugs.


Abstract

In the present manuscript, we have reported a general catalytic strategy that allows the synthesis of a variety of difluoro methylated alkanes from the corresponding unactivated alkenes using commercially available radical difluoromethylating reagent (CF2HSO2Na) under visible light photocatalysis. Further, this strategy allows the late-stage modification of various alkenes derived from pharmaceutically relevant drugs.

Verwandte Artikel

Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis
54. Deutsche Lebensmittelchemietage 2026 in Kaiserslautern
Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis
GDCh-Fachgruppe Patentrecht schreibt Innovationspreis 2027 aus
Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis
Primo Levi. His legacy still bonds chemistry and conscience.
Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis
„Alles Chlor!“: 088 Schaumgeflüster
Hydrodifluoromethylation of unactivated alkenes enabled by Visible‐Light Photocatalysis
GDCh ehrt Ullrich Scherf mit Hermann-Staudinger-Preis