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Stille coupling alcohol oxidation

The activity of elemental carbon as a metal-free catalyst is well established for a couple of reactions, however, most literature still deals with the support properties of this material. The discovery of nanostructured carbons in most cases led to an increased performance for the abovementioned reasons, thus these systems attracted remarkable research interest within the last years. The most prominent reaction is the oxidative dehydrogenation (ODH) of ethylbenzene and other hydrocarbons in the gas phase, which will be introduced in a separate chapter. The conversion of alcohols as well as the catalytic properties of graphene oxide for liquid phase selective oxidations will also be discussed in more detail. The third section reviews individually reported catalytic effects of nanocarbons in organic reactions, as well as selected inorganic reactions. [Pg.401]

Aldol reaction, oxidation (alcohol —> ketone), aromatie metalation (nBuLi), Pd(0)-mediated coupling reactions (Heck, Stille, Suzuki). [Pg.214]

See other pages where Stille coupling alcohol oxidation is mentioned: [Pg.243]    [Pg.397]    [Pg.492]    [Pg.365]    [Pg.636]    [Pg.63]    [Pg.658]    [Pg.397]    [Pg.595]    [Pg.610]    [Pg.37]    [Pg.631]    [Pg.204]    [Pg.306]    [Pg.24]    [Pg.197]    [Pg.281]    [Pg.275]    [Pg.702]    [Pg.1238]    [Pg.1243]    [Pg.157]    [Pg.163]    [Pg.240]    [Pg.423]    [Pg.967]    [Pg.967]    [Pg.137]    [Pg.300]    [Pg.577]    [Pg.17]    [Pg.137]    [Pg.287]    [Pg.148]    [Pg.551]    [Pg.244]    [Pg.300]    [Pg.827]    [Pg.316]    [Pg.344]    [Pg.224]    [Pg.534]    [Pg.7]    [Pg.162]    [Pg.60]    [Pg.5450]    [Pg.276]    [Pg.100]   
See also in sourсe #XX -- [ Pg.204 ]



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