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Potier—Polonovski rearrangement

Vinylogous trifluoromethyl amides. The Potier-Polonovski rearrangement of tertiary amine A(-oxides induced by (CFjCOjjO is frequently followed by trifluoroacetylation. This method is most suitable for the synthesis of (-)-altemicidin. ... [Pg.361]

See other pages where Potier—Polonovski rearrangement is mentioned: [Pg.136]    [Pg.136]    [Pg.356]    [Pg.74]    [Pg.2251]    [Pg.129]    [Pg.655]    [Pg.101]    [Pg.95]   
See also in sourсe #XX -- [ Pg.470 ]

See also in sourсe #XX -- [ Pg.442 ]

See also in sourсe #XX -- [ Pg.488 ]

See also in sourсe #XX -- [ Pg.319 ]

See also in sourсe #XX -- [ Pg.288 ]

See also in sourсe #XX -- [ Pg.442 ]



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Polonovski

Polonovski rearrangement

Potier—Polonovski

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