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Hofmann rearrangement stereoselectivity

Generally, hypervalent iodine reagents are often better than traditional reagents of similar reactivity, with respect to efficiency and chemoselectivity - sometimes even stereoselectivity. Unusual reactivity is another interesting feature which has often resulted in unexpected transformation. Examples of such reactions may be found in the oxidation of nitrogen-containing compounds, the Hofmann rearrangement in acidic conditions, the acetalization of carbonyl compounds in alkali, the remote functionalization of steroids, etc. Some unique transformations were effected in the... [Pg.6]


See other pages where Hofmann rearrangement stereoselectivity is mentioned: [Pg.356]    [Pg.223]   
See also in sourсe #XX -- [ Pg.6 , Pg.798 ]

See also in sourсe #XX -- [ Pg.798 ]

See also in sourсe #XX -- [ Pg.6 , Pg.798 ]

See also in sourсe #XX -- [ Pg.798 ]




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Hofmann rearrangement

Rearrangements stereoselective

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