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SCHWEIZER Allylamine synthesis

SCHWARTZ Hydrolirconation 339 SCHWEIZER Allylamine synthesis 340 SCHWEIZER Rearrangement 341 Semidina 434... [Pg.455]

An investigation of the synthesis of allylamines via vinylphosphonium salts (Schweizer reaction), has displayed its generality for their preparation in high stereochemical purity. Thus, the reaction between phthalimide, vinyltri-n-butylphosphonium bromide, and an aldehyde in the presence of sodium hydride gives the H-imide (8), from which the free -allylamines can be liberated (Scheme 10). Ketones do not react. [Pg.196]

See other pages where SCHWEIZER Allylamine synthesis is mentioned: [Pg.328]    [Pg.328]    [Pg.97]   
See also in sourсe #XX -- [ Pg.340 ]

See also in sourсe #XX -- [ Pg.340 ]

See also in sourсe #XX -- [ Pg.340 ]



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Allylamine

Allylamines synthesis

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