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Alcohol Oxidation in Organic Chemistry

Alcohol oxidation to form carbonyhc compounds is one of the pivotal functional group transformations of organic chemistry [88]. Classical organic syntheses are [Pg.406]

Transition metals Mn04, Mn02, Cr207 Cr04 CrOs, Pb(OAc)4, Cu, Ag Haiooxo acids I04, Br04, CI04, CIO  [Pg.408]

Related Precedents to the Use of Cold Catalysts for the Aerobic Oxidation of Alcohols [Pg.408]

In recent years there have been important steps towards the development of these ideal aerobic oxidations. Thus, Mizuno and coworkers reported a new generation of ruthenium oxide that acts as a heterogeneous catalyst for the oxidation of alcohols [95, 96]. The main drawbacks of this process were, however, the need for high oxgyen pressure and the fact that the catalyst is moisture sensitive. Both disadvantages constituted a serious limitation of the process. [Pg.408]

An additional problem arises from the need for high oxygen pressure to effect alcohol oxidation. [Pg.409]


See other pages where Alcohol Oxidation in Organic Chemistry is mentioned: [Pg.406]    [Pg.407]   


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