Acid-catalyzed rearrangements in arenes: interconversions in the quaterphenyl series

Arenes undergo rearrangement of phenyl, alkyl, halogen and other groups through the intermediacy of ipso arenium ions in which a proton is attached at the same carbon as the migrating substituent. Interconversions among the six quaterphenyl isomers have been studied here as a model for rearrangement...

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Bibliographic Details
Main Authors: Sarah L. Skraba-Joiner, Carter J. Holt, Richard P. Johnson
Format: Article
Language:English
Published: Beilstein-Institut 2019-11-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.15.258