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Beilstein J. Org. Chem. 2024, 20, 257–263, doi:10.3762/bjoc.20.26
Graphical Abstract
Scheme 1: Synthetic application of thianthrenium salts.
Scheme 2: Substrate scope. Reaction conditions: alkylthianthrenium salts 1 (0.3 mmol), thiophenols 2 (0.2 mmo...
Scheme 3: Substrate scope of amines. Reaction conditions: alkylthianthrenium salts 1 (0.3 mmol), amines 2 (0....
Scheme 4: Scale-up reaction.
Beilstein J. Org. Chem. 2023, 19, 1562–1567, doi:10.3762/bjoc.19.113
Figure 1: Natural products and drug molecules containing isoxazole moieties.
Scheme 1: Traditional methods for the synthesis of isoxazoles and the current approach.
Scheme 2: Reaction scope of alkynes. Conditions: 1 (0.1 mmol, 1 equiv), 2a (0.2 mmol, 2 equiv), AlCl3 (0.3 mm...
Figure 2: Crystal structure of 3i.
Scheme 3: Reaction substrate scope of quinolines. Conditions: 1a (0.1 mmol, 1 equiv), 2 (0.2 mmol, 2 equiv), ...
Scheme 4: Gram scale reaction.
Scheme 5: Control experiments and possible reaction mechanism.
Beilstein J. Org. Chem. 2022, 18, 647–652, doi:10.3762/bjoc.18.65
Scheme 1: Amination of arenes with phthalimides.
Scheme 2: Substrate scope of the copper-catalyzed C–H imidation of arenes. Reaction conditions: 1 (2.0 mL as ...
Scheme 3: Substrate scope of the copper-catalyzed C–H imidation of N-hydroxyphthalimide. Reaction conditions: ...
Scheme 4: A plausible reaction mechanism.