This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2026, 22, 1122–1150, doi:10.3762/bjoc.22.91
Graphical Abstract
Figure 1: FDA-approved drugs containing CF2 groups (2016–2025). a) For tezacaftor (4), the 2018 approval year...
Figure 2: Synthesis of the alkyl–CF2 side chain in glecaprevir (1) and voxilaprevir (2).
Figure 3: Synthesis of the difluorinated intermediate 38 for ivosidenib (3).
Figure 4: Synthesis of the difluorinated intermediate for cedazuridine (5).
Figure 5: Synthesis of the difluorinated intermediate for omaveloxolone (10).
Figure 6: Synthesis of the difluorinated intermediate for 1-(perfluorohexyl)octane (11).
Figure 7: Synthetic routes towards difluorinated intermediates for the synthesis of inavolisib.
Figure 8: Synthesis of the difluorinated intermediate for glecaprevir.
Figure 9: Synthesis of the difluorinated intermediate for voxilaprevir.
Figure 10: Synthesis of the difluorinated intermediate for lenacapavir.
Figure 11: Synthesis of the difluorinated intermediate for oteseconazole.
Figure 12: Synthesis of the difluorinated intermediate for tezacaftor.
Figure 13: Synthesis of the difluorinated intermediate for difamilas (6).
Figure 14: Synthesis of the difluorinated intermediate for asciminib.
Figure 15: Mechanism of the deoxyfluorination of carbonyl groups using DAST.
Figure 16: Mechanism of the deoxyfluorination of carbonyl groups using SF4.
Figure 17: Mechanism of the fluorination of dithioketals using Olah’s reagent.
Figure 18: Mechanism of the fluorination of xanthates using AgF.
Figure 19: Mechanism of electrophilic fluorination using NFSI.
Figure 20: Mechanism of the Ni-catalyzed conversion of Ar–X to Ar–CF2H using Hu’s reagent.
Figure 21: Mechanism of the (Me3Si)3SiH-mediated intermolecular perfluoroalkylation of alkenes in water.
Figure 22: Mechanism of the formation of ArO–CF2H from ClF2COONa and ArOH.
Figure 23: Mechanism of the formation of ArO–CF2X from TMSCF2X and ArOH.