Jump to main content
Jump to site search

Issue 21, 2005
Previous Article Next Article

First transamination reactions for the one-pot synthesis of substituted zwitterionic quinones

Author affiliations

Abstract

A new and very efficient one-pot synthesis, in water, of 6π + 6π electron zwitterionic benzoquinonemonoimines involves the first examples of transamination reactions in quinonoid chemistry and allows the introduction of functionalities to, and the fine-tuning of the properties of, a large family of molecules with interesting potential, both in supramolecular chemistry and as multidentate ligands in coordination chemistry.

Graphical abstract: First transamination reactions for the one-pot synthesis of substituted zwitterionic quinones

Back to tab navigation

Supplementary files

Publication details

The article was received on 10 Feb 2005, accepted on 22 Mar 2005 and first published on 06 Apr 2005


Article type: Communication
DOI: 10.1039/B501926E
Citation: Chem. Commun., 2005,0, 2660-2662
  •   Request permissions

    First transamination reactions for the one-pot synthesis of substituted zwitterionic quinones

    Q. Yang, O. Siri and P. Braunstein, Chem. Commun., 2005, 0, 2660
    DOI: 10.1039/B501926E

Search articles by author

Spotlight

Advertisements