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8-substituted-pterin substrates

The majority of reported reactions of aryl and heteroaryl substrates with organocopper reagents are examples of Stephens-Castro coupling or the more recent catalytic version of that reaction. The reaction has found recent application in syntheses of C-(6)-substituted pterins and pteridines, substituted pyridines, and the antitumor antibiotic fredericamycin A," to name a few. Aryl iodide can be che-mospecifically displaced in the presence of bromide," and 2,5-dibromopyridine is regioselectively substituted at the 2-position. Substitution of halobenzenes by propargyl alcohol, followed by oxidative cleavage, provides a convenient route to terminal arylalkynes. " Fused heterocycles are formed in reactions of aryl halides bearing nucleophilic ortho substituents. - "... [Pg.219]


See other pages where 8-substituted-pterin substrates is mentioned: [Pg.344]    [Pg.344]    [Pg.346]    [Pg.359]    [Pg.344]    [Pg.344]    [Pg.346]    [Pg.359]    [Pg.309]    [Pg.932]    [Pg.160]    [Pg.150]    [Pg.702]    [Pg.396]    [Pg.70]    [Pg.1744]    [Pg.382]    [Pg.2257]    [Pg.382]    [Pg.332]   
See also in sourсe #XX -- [ Pg.344 , Pg.346 , Pg.355 ]




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