Reactions · Wikipedia: Category:Name reactions

Pschorr cyclization

Overview

The Pschorr cyclization is a name reaction in organic chemistry, which was named after its discoverer, the German chemist Robert Pschorr (1868-1930). It describes the intramolecular substitution of aromatic compounds via aryldiazonium salts as intermediates and is catalyzed by copper. The reaction is a variant of the Gomberg-Bachmann reaction. The following reaction scheme shows the Pschorr cyclization for the example of phenanthrene:

Actions

  • This entry doesn't have stoichiometric equivalents on file yet — the Reaction Scale Calculator needs at least one participant tagged with an equivalents value.
  • Mechanism / source ↗

Recent Searches

Acetone
Ethanol
Navigate
esc Close