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Rearrangement Stieglitz

The name Stieglitz rearrangement is generally applied to the rearrangements of... [Pg.1417]

The name Stieglitz rearrangement is generally applied to the rearrangements of trityl N-haloamines and hydroxylamines. These reactions are similar to the rearrangements of alkyl... [Pg.1097]

A migration of an aryl group from carbon to nitrogen takes place also in the Stieglitz rearrangement. For example, the benzylamine derivatives 234 were converted into anils 235 in a reaction induced by p-nitrobenzenesulfonyl peroxide (p-NBSP)337 (equation 94). [Pg.628]

Stieglitz rearrangement. Rearrangement of trityl hydroxylamines to Schiff bases on treatment with phosphorous pentachloride. [Pg.1179]

This reaction is related to the Curtius Rearrangement, Hofmann Rearrangement, Lossen Rearrangement, and Stieglitz Rearrangement. [Pg.2507]

Stevens (see McFadyen-Stevens Reaction) Stevens Rearrangement Stieglitz Rearrangement Stille Coupling Stobbe Condensation... [Pg.15]

See other pages where Rearrangement Stieglitz is mentioned: [Pg.1417]    [Pg.164]    [Pg.1097]    [Pg.455]    [Pg.1617]    [Pg.434]    [Pg.434]    [Pg.504]    [Pg.413]    [Pg.712]    [Pg.391]    [Pg.357]    [Pg.337]   
See also in sourсe #XX -- [ Pg.365 ]

See also in sourсe #XX -- [ Pg.1416 ]

See also in sourсe #XX -- [ Pg.1097 ]

See also in sourсe #XX -- [ Pg.1616 ]

See also in sourсe #XX -- [ Pg.365 ]

See also in sourсe #XX -- [ Pg.504 , Pg.505 ]

See also in sourсe #XX -- [ Pg.391 ]

See also in sourсe #XX -- [ Pg.357 ]



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