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Cycloalkanone oxidative ring opening

Oxidative Cleavage of Ketones. Aldehydes, and Alcohols Cycloalkanone oxidative ring opening... [Pg.1176]

Greater preparative importance attaches to oxidative ring opening of cycloalkanols and cycloalkanones, which then afford alkanedioic acids containing an unchanged number of carbon atoms. Thus, for instance, adipic acid is obtained in up to 90% yield from cyclohexanol or cyclohexanone by means of about 60% nitric acid containing vanadium and copper salts as catalyst 125... [Pg.1040]


See other pages where Cycloalkanone oxidative ring opening is mentioned: [Pg.1521]    [Pg.1521]    [Pg.1103]   
See also in sourсe #XX -- [ Pg.1176 ]




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