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Beilstein J. Org. Chem. 2020, 16, 3032–3037, doi:10.3762/bjoc.16.252
Graphical Abstract
Scheme 1: State of the art concerning the direct nucleophilic trifluoromethylselenolation.
Scheme 2: The nucleophilic fluoroalkylselenolation of alkyl bromides. Yields were determined by 19F NMR spect...
Scheme 3: Mechanism proposal.
Beilstein J. Org. Chem. 2017, 13, 2626–2630, doi:10.3762/bjoc.13.260
Scheme 1: Electrophilic addition of 1a to alkynes. Yields shown are those of isolated products; yields determ...
Figure 1: Single-crystal X-ray structure of 3a.
Scheme 2: Mechanism proposal.
Scheme 3: Perfluoroalkylselenolation of alkynes. Yields shown are those of isolated products; yields determin...
Beilstein J. Org. Chem. 2013, 9, 2354–2357, doi:10.3762/bjoc.9.270
Figure 1: Transamination of 1a with amines. (Isolated yields, in parentheses crude yields determined by 19F N...
Figure 2: Reaction of 1a with bis-nucleophiles. (Isolated yields, in parentheses crude yields determined by 19...
Figure 3: Synthesis of fluoroalkylthio analogs of imipramine. (Isolated yields, in parentheses crude yields d...