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Nitronate structures general reactivity

Compounds of structures (14)-(16) are in general less studied than all other classes of (oxa/thia)-2-azoles, either because of difficulty in their preparation or their thermal instability. Some of them are stable, but others are nonisolable reactive intermediates <75S205). The dioxazolidine (137) is reversibly dissociated to the nitrone and pivalaldehyde <80JCR(S)122> (Equation (2)) the dioxazolidine (138) is more stable, but decomposes on heating at 300°C to yield the pivalaldehyde (Bu CH=0) and the benzimidazolone (139) (Equation (3)) <86JOC732). [Pg.519]


See other pages where Nitronate structures general reactivity is mentioned: [Pg.357]    [Pg.357]    [Pg.357]    [Pg.2039]   
See also in sourсe #XX -- [ Pg.105 , Pg.106 , Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 ]

See also in sourсe #XX -- [ Pg.105 , Pg.106 , Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 ]




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General reactivity

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Nitronates structure

Structural generalization

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