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Named rearrangements Friedel-Crafts

Several name reactions are promoted by AICI3. For example, the Darzens-Nenitzescu reaction is simply the acylation of alkenes. The Ferrario reaction generates phenoxathiins from diphenyl ethers (eq 19) The rearrangement of acyloxy aromatic systems is known as the Fries rearrangement (eq 20). Aryl aldehydes are produced by the Gatterman aldehyde synthesis (eq 21). The initial step of the Haworth phenanthrene synthesis makes use of a Friedel-Crafts acylation. The acylation of phenolic cort tounds is called the Houben-Hoesch reaction (eq 22). The Leuckart amide s)oithesis generates aryl amides from isocyanates (eq 23). ... [Pg.20]


See other pages where Named rearrangements Friedel-Crafts is mentioned: [Pg.725]    [Pg.145]    [Pg.725]    [Pg.71]    [Pg.725]    [Pg.1006]    [Pg.61]    [Pg.1006]    [Pg.725]    [Pg.231]    [Pg.617]    [Pg.725]    [Pg.28]    [Pg.324]    [Pg.145]   
See also in sourсe #XX -- [ Pg.511 , Pg.518 ]




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Friedel-Crafts rearrangements

Named rearrangements

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