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Quinolinium bromochromate

Dimethylpyrazolinium fluorochromate,403 isoquinolinium fluorochromate (iQFC)404 and quinolinium bromochromate (QBC)405 have also been described as halochromates able to oxidize alcohols. [Pg.88]

Several reports deal with the action of heterocycle-chromate agents such as quinolin-ium dichromate on five-membered heteroaldehydes340 and quinolinium bromochromate on benzaldehydes,341,342 all in acetic acid solution. The latter studies show a second-order dependence on proton concentration, acceleration by electron-withdrawing para-substituents, and a substantial kinetic isotope effect for the deuterated aldehyde. [Pg.42]

Oxidation of several primary aliphatic alcohols with potassium dichromate, pyri-dinium dichromate, quinolinium dichromate (QDC), imidazolium dichromate, nico-tinium dichromate, isonicotinium dichromate, pyridinium fluorochromate (PFC), quinolinium fluorochromate, imidazolium fluorochromate, pyridinium chlorochromate (PCC), quinolinium chlorochromate (QCC), and pyridinium bromochromate (PBC), in aqueous acetic acid and in the presence of perchloric acid, showed similar kinetics. The values of the reaction constants did not differ significantly, indicating operation of a common mechanism.1... [Pg.85]


See other pages where Quinolinium bromochromate is mentioned: [Pg.93]    [Pg.86]    [Pg.278]    [Pg.93]    [Pg.86]    [Pg.278]    [Pg.88]   
See also in sourсe #XX -- [ Pg.42 , Pg.93 ]

See also in sourсe #XX -- [ Pg.279 ]

See also in sourсe #XX -- [ Pg.5 , Pg.104 ]




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