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Selenium compounds secondary alcohols

A mixture of 1,4-dioxane and water is often used as the solvent for the conversion of aldehydes and ketones by H2Se03 to a-dicarbonyl compounds in one step (Eq. 8.117).331 Dehydrogenation of carbonyl compounds with selenium dioxide generates the a, (i-unsaturated carbonyl compounds in aqueous acetic acid.332 Using water as the reaction medium, ketones can be transformed into a-iodo ketones upon treatment with sodium iodide, hydrogen peroxide, and an acid.333 Interestingly, a-iodo ketones can be also obtained from secondary alcohol through a metal-free tandem oxidation-iodination approach. [Pg.281]


See other pages where Selenium compounds secondary alcohols is mentioned: [Pg.319]    [Pg.489]    [Pg.1619]    [Pg.820]    [Pg.1098]    [Pg.694]    [Pg.24]    [Pg.589]    [Pg.196]    [Pg.321]   
See also in sourсe #XX -- [ Pg.323 ]

See also in sourсe #XX -- [ Pg.323 ]

See also in sourсe #XX -- [ Pg.7 , Pg.323 ]

See also in sourсe #XX -- [ Pg.7 , Pg.323 ]

See also in sourсe #XX -- [ Pg.323 ]




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Selenium compounds

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