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Pyrrole 2-acyl-, acid-catalyzed rearrangement

The acid-catalyzed rearrangements of substituted pyrroles and thiophenes consequent on ipso protonation have been referred to previously (Section 3.02.2.4.2). There is some evidence that these rearrangements are intramolecular in nature since in the case of acid-induced rearrangement of 2-acylpyrroles to 3-acylpyrroles no intermolecular acylation of suitable substrates could be demonstrated (Scheme 10) (8UOC839). [Pg.48]


See other pages where Pyrrole 2-acyl-, acid-catalyzed rearrangement is mentioned: [Pg.304]    [Pg.44]    [Pg.225]    [Pg.44]    [Pg.396]    [Pg.168]    [Pg.44]    [Pg.169]    [Pg.169]    [Pg.208]    [Pg.221]    [Pg.208]    [Pg.221]    [Pg.225]    [Pg.111]   
See also in sourсe #XX -- [ Pg.307 ]




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Acid-catalyzed rearrangements

Acylals, rearrangement

Acylation acid catalyzed

Pyrrole acidity

Pyrrole, 3- acylation

Pyrrole, 3-acyl

Pyrroles rearrangement

Pyrrolic acids

Rearrangement 4-acyl

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