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Ketenimines reactions with Fischer carbene complexes

The metal-free eyclobutane-1,2-dioxime can be generated by oxidative displacement. It is interesting to note that, unlike ketene dimerization, head-to-head dimerization takes place here. The chromium ketenimine complex 20 is prepared by reaction of the Fischer-type chromium carbene complex with alkyl isocyanides.60 A cyclobutane-1,2,3,4-tetraimine 24 has been reported from the reaction of the ketenimine phosphonium ylide 22.61 Bisimine 23 has been proposed as the intermediate in this transformation. [Pg.99]


See other pages where Ketenimines reactions with Fischer carbene complexes is mentioned: [Pg.1109]    [Pg.1109]   
See also in sourсe #XX -- [ Pg.1109 ]

See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.1109 ]

See also in sourсe #XX -- [ Pg.5 ]




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Carbene Fischer carbenes

Carbene complexes reactions

Carbene reactions

Carbenes Fischer carbene complexes

Carbenes reactions

Complexes Fischer

Fischer carbene

Fischer carbene complexes

Fischer reactions

Ketenimine

Ketenimines

Reaction with carbenes

Reaction with ketenimines

With Carbenes

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