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Selenoxide, benzyl phenyl synthesis

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 Selenoxide, benzyl phenyl synthesis is mentioned: [Pg.235]    [Pg.505]   
See also in sourсe #XX -- [ Pg.772 ]

See also in sourсe #XX -- [ Pg.772 ]

See also in sourсe #XX -- [ Pg.7 , Pg.772 ]

See also in sourсe #XX -- [ Pg.7 , Pg.772 ]

See also in sourсe #XX -- [ Pg.772 ]




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Benzyl phenyl

Selenoxide

Selenoxides

Synthesis selenoxide

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