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Aromatic nucleophilic denitrocyclization reactions

Finally, aromatic nucleophilic denitrocyclization reactions are reviewed for the first time by Stanislav Radi (Prague, Czech Republic). The nitro functionality is a good leaving group, especially for intramolecular reactions, and many such reactions lead to polycyclic heterocyclic ring systems. Frequently, these transformations are a method of choice for preparative purposes. [Pg.261]

Aromatic nucleophilic denitrocyclization reactions leading to annulated five-, six-, seven-, and eight-membered heterocycles 02AHC(83)189. [Pg.154]

See other pages where Aromatic nucleophilic denitrocyclization reactions is mentioned: [Pg.189]    [Pg.191]    [Pg.193]    [Pg.195]    [Pg.197]    [Pg.199]    [Pg.201]    [Pg.203]    [Pg.205]    [Pg.207]    [Pg.209]    [Pg.211]    [Pg.213]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.231]    [Pg.233]    [Pg.235]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.247]    [Pg.249]    [Pg.251]    [Pg.253]    [Pg.255]    [Pg.303]    [Pg.321]   
See also in sourсe #XX -- [ Pg.83 , Pg.189 ]

See also in sourсe #XX -- [ Pg.83 , Pg.189 ]

See also in sourсe #XX -- [ Pg.83 , Pg.189 ]

See also in sourсe #XX -- [ Pg.83 , Pg.189 ]



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