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Imidazole-2,4 -diones generation, reactions

Nucleophilic attack of substituted alkylamines including benzylamines to 6,7-dihydro-imidazo[l,2- ]imidazole-2,5-diones 34, cleaved the imidazolidinone ring to generate the acetamide derivatives 81 (Equation 34) <1998APH389, 2001JST73>. Reaction of the tricyclic thiazolium salt 45 with methoxylamine gave the oxime 82 (Equation 35) <1999JME2828>. [Pg.143]

See other pages where Imidazole-2,4 -diones generation, reactions is mentioned: [Pg.315]    [Pg.173]    [Pg.475]    [Pg.241]    [Pg.255]    [Pg.475]    [Pg.23]    [Pg.255]    [Pg.166]    [Pg.216]    [Pg.551]   
See also in sourсe #XX -- [ Pg.58 , Pg.195 ]



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Imidazole-2,4 -diones

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