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Synthesis of pyridines by electrochemical methods

Yoshida and coworkers developed a method for C-H nitrogenation of aromatics based on electrochemical oxidation of aromatic compounds in the presence of pyridine followed by the reaction of the resulting A -arylpyridinium ions with piperidine to selectively give aromatic primary amines as products [108]. This transformation provides a metal-free protocol for one-pot synthesis aromatic amines with broad functional groups compatibility (Scheme 2.10). [Pg.21]

See other pages where Synthesis of pyridines by electrochemical methods is mentioned: [Pg.167]    [Pg.377]    [Pg.300]    [Pg.339]    [Pg.300]    [Pg.23]    [Pg.206]    [Pg.290]    [Pg.321]    [Pg.350]    [Pg.350]    [Pg.323]    [Pg.167]    [Pg.377]    [Pg.300]    [Pg.339]    [Pg.300]    [Pg.23]    [Pg.206]    [Pg.290]    [Pg.321]    [Pg.350]    [Pg.350]    [Pg.323]    [Pg.167]    [Pg.509]    [Pg.358]    [Pg.194]    [Pg.233]    [Pg.2387]    [Pg.264]    [Pg.105]    [Pg.375]    [Pg.302]   
See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]

See also in sourсe #XX -- [ Pg.37 , Pg.167 ]



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