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Hydrogenation-Baeyer-Villiger oxidation reaction

Tandem hydrogenation-Baeyer-Villiger oxidation reaction catalysed by rhodium catalysis and biocatalysis. [Pg.186]

Urea hydrogen peroxide adduct (UHP) was employed in metal-catalysed asymmetric epoxidation [98] and Baeyer-Villiger oxidation [99,100]. Since the presence of urea does not change the course of the reaction, this will not be described here. Conversion of epoxides to halohydrins with elemental... [Pg.247]

In 2001, Albrecht Berkessel and Nadine Vogl reported on the Baeyer-Villiger oxidation with hydrogen peroxide in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as solvent in the presence of Brpnsted acid catalysts such as para-toluenesulfonic acid (equation 85) . Under these conditions cyclohexanone could be selectively transformed into the corresponding lactone within 40 min at 60 °C with a yield of 92%. Mechanistic investigations of Berkessel and coworkers revealed that this reaction in HFIP proceeds by a new mechanism, via spiro-bisperoxide 234 as intermediate, which then rearranges to form the lactone. The study illustrates the importance of HFIP as solvent for the reaction, which presumably allows the cationic rearrangement of the tetroxane intermediates. [Pg.556]

The recent development of inorganic crystalline-supported metal catalysts for various liquid-phase oxidation reactions such as alcohol oxidation, epoxidation, Baeyer-Villiger oxidation and oxidation via C—H activation using molecular oxygen (02) or hydrogen peroxide (H202) as an oxidant are reviewed in this chapter. [Pg.157]

Iodine-catalysed hydroperoxidation of cyclic and acyclic ketones with aqueous hydrogen peroxide in acetonitrile is an efficient and eco-friendly method for the synthesis of gem -dihydroperoxides and the reaction is conducted in a neutral medium with a readily available low-cost oxidant and catalyst.218 Aryl benzyl selenoxides, particularly benzyl 3,5-bis(trifluoromethyl)phenyl selenoxide, are excellent catalysts for the epoxidation of alkenes and Baeyer-Villiger oxidation of aldehydes and ketones with hydrogen peroxide.219 Efficient, eco-friendly, and selective oxidation of secondary alcohols is achieved with hydrogen peroxide using aqueous hydrogen bromide as a catalyst. Other peroxides such as i-butyl hydroperoxide (TBHP), sodium... [Pg.115]


See other pages where Hydrogenation-Baeyer-Villiger oxidation reaction is mentioned: [Pg.186]    [Pg.186]    [Pg.540]    [Pg.540]    [Pg.3188]    [Pg.107]    [Pg.107]    [Pg.76]    [Pg.78]    [Pg.113]    [Pg.113]    [Pg.44]    [Pg.46]    [Pg.298]    [Pg.544]    [Pg.544]    [Pg.548]    [Pg.18]    [Pg.263]    [Pg.368]    [Pg.543]    [Pg.544]    [Pg.544]    [Pg.548]    [Pg.556]    [Pg.154]    [Pg.650]    [Pg.195]    [Pg.195]    [Pg.105]    [Pg.625]    [Pg.304]    [Pg.350]    [Pg.51]    [Pg.113]    [Pg.113]    [Pg.79]    [Pg.62]   
See also in sourсe #XX -- [ Pg.166 ]




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