Jump to main content
Jump to site search

Issue 41, 2011
Previous Article Next Article

Asymmetric Brønsted acid catalyzed carbonyl activation – organocatalytic domino electrocyclization–halogenation reaction

Author affiliations

Abstract

A highly efficient Brønsted acid catalyzed enantioselective Nazarov cyclization–bromination reaction has been developed. The protocol gives access to highly functionalized trans-4,5-substituted 5-bromocyclopentenone derivatives in good yields and with excellent enantioselectivities.

Graphical abstract: Asymmetric Brønsted acid catalyzed carbonyl activation – organocatalytic domino electrocyclization–halogenation reaction

Back to tab navigation

Supplementary files

Publication details

The article was received on 25 Aug 2011, accepted on 25 Aug 2011 and first published on 05 Sep 2011


Article type: Communication
DOI: 10.1039/C1CC15289K
Chem. Commun., 2011,47, 11450-11452

  •   Request permissions

    Asymmetric Brønsted acid catalyzed carbonyl activation – organocatalytic domino electrocyclization–halogenation reaction

    M. Rueping and W. Ieawsuwan, Chem. Commun., 2011, 47, 11450
    DOI: 10.1039/C1CC15289K

Search articles by author

Spotlight

Advertisements