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Beilstein J. Org. Chem. 2020, 16, 1550–1553, doi:10.3762/bjoc.16.126
Graphical Abstract
Scheme 1: Reactions of (bromodifluoromethyl)trimethylsilane (1).
Scheme 2: Optimization studies. Yield determined by 19F NMR spectroscopy using an internal standard.
Figure 1: Reaction of silyl enol ethers. Yields refer to isolated yields. aReaction time 24 h; b1.0 equiv of ...
Scheme 3: Proposed mechanism of the fluoroalkylation reaction.
Beilstein J. Org. Chem. 2018, 14, 1637–1641, doi:10.3762/bjoc.14.139
Scheme 1: Fluoroalkylation of alkenes.
Figure 1: Difluoroalkylation of alkenes. Isolated yields are shown. a2 equiv of the alkene were used.
Scheme 2: Proposed mechanism.
Beilstein J. Org. Chem. 2015, 11, 2145–2149, doi:10.3762/bjoc.11.231
Scheme 1: Reaction of organozinc compounds.