p-Anisidine can undergo aerobic oxidation in the presence of gold catalysts to form aromatic azo compounds. p-Anisidine can be used:
In the diastereoselective and enantioselective synthesis of CF3-substituted azoridines catalyzed by a chiral Bronsted acid.
To prepare 4-organoselenium-quinolines through multi-component Povarov reaction with ethyl glyoxylate and ethynyl(phenyl)selane, catalyzed by Yb(OTf)3.
As a starting material to synthesize 3-fluoro-6-methoxyquinoline in two steps.,
To prepare N-PMP protected α-aminopropargylphosphonates by reacting with terminal alkynes and diethyl formylphosphonate hydrate using silver(I) triflate as a catalyst.
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