Photoredox Activation and Anion Binding Catalysis in the Dual Catalytic Enantioselective Synthesis of β-Amino Esters

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...

Full description

Saved in:
Bibliographic Details
Published inChemical science (Cambridge) Vol. 5; no. 1; pp. 112 - 116
Main Authors Bergonzini, Giulia, Schindler, Corinna S, Wallentin, Carl-Johan, Jacobsen, Eric N, Stephenson, Corey R J
Format Journal Article
LanguageEnglish
Published England 01.01.2014
Online AccessGet full text

Cover

More Information
Summary: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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2041-6520
2041-6539
DOI:10.1039/c3sc52265b