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

Article information


Submitted
12 Aug 2013
Accepted
22 Aug 2013
First published
23 Aug 2013

Chem. Sci., 2014,5, 112-116
Article type
Edge Article

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

Social activity

Search articles by author

Spotlight

Advertisements