Jump to main content
Jump to site search

Issue 1, 2014
Previous Article Next Article

Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters

Author affiliations

Abstract

The enantioselective oxidative C–H functionalization of tetrahydroisoquinoline derivatives is achieved through the merger of photoredox and asymmetric anion-binding catalysis. This combination of two distinct catalysis concepts introduces a potentially general approach to asymmetric transformations in oxidative photocatalysis.

Graphical abstract: Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters

Back to tab navigation

Supplementary files

Publication details

The article was received on 12 Aug 2013, accepted on 22 Aug 2013 and first published on 23 Aug 2013


Article type: Edge Article
DOI: 10.1039/C3SC52265B
Citation: Chem. Sci., 2014,5, 112-116
  •   Request permissions

    Photoredox activation and anion binding catalysis in the dual catalytic enantioselective synthesis of β-amino esters

    G. Bergonzini, C. S. Schindler, C. Wallentin, E. N. Jacobsen and C. R. J. Stephenson, Chem. Sci., 2014, 5, 112
    DOI: 10.1039/C3SC52265B

Search articles by author

Spotlight

Advertisements