Jump to main content
Jump to site search

Issue 51, 2012
Previous Article Next Article

Desymmetrization of cyclohexadienones viaD-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

Author affiliations

Abstract

Enantioselective desymmetrization of cyclohexadienones via a D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction was realized. With 10 mol% of camphor-derived triazolium salt E and 10 mol% of DIEA, various substituted cyclohexadienones proceeded through an intramolecular Stetter reaction, affording tricyclic products in moderate to good yields and excellent ee.

Graphical abstract: Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

Back to tab navigation

Supplementary files

Publication details

The article was received on 19 Apr 2012, accepted on 08 May 2012 and first published on 10 May 2012


Article type: Communication
DOI: 10.1039/C2CC32783J
Citation: Chem. Commun., 2012,48, 6363-6365
  •   Request permissions

    Desymmetrization of cyclohexadienones viaD-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

    M. Jia and S. You, Chem. Commun., 2012, 48, 6363
    DOI: 10.1039/C2CC32783J

Search articles by author

Spotlight

Advertisements