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Muscarinic M3 antagonists

The copper-catalyzed amination of bromopyridine 29 was reported by workers at Merck on route to the synthesis of muscarinic (M3) antagonist 31 <01TL3251>. Interestingly, an uncatalyzed amination of 3-nitropyridines has also been reported <01JCS(P1)376>. Other metal mediated processes have been used to access pyridines with important biological activity as well <0lJOC605x01TL6811>. [Pg.261]


See other pages where Muscarinic M3 antagonists is mentioned: [Pg.99]    [Pg.474]    [Pg.344]    [Pg.321]   
See also in sourсe #XX -- [ Pg.53 , Pg.58 , Pg.329 ]

See also in sourсe #XX -- [ Pg.576 ]




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