| Literature DB >> 29265675 |
Line Naesborg1, Vasco Corti1, Lars Astrup Leth1, Pernille H Poulsen1, Karl Anker Jørgensen1.
Abstract
A novel concept for catalytic asymmetric coupling reactions is presented. Merging organocatalysis with single-electron oxidation by using a catalytic amount of a copper(II) salt and air as the terminal oxidant, we have developed a highly stereoselective carbon-carbon oxidative coupling reaction of α,β-unsaturated aldehydes. The concept relies on the generation of a dienamine intermediate, which is oxidized to an open-shell activated species that undergoes highly selective γ-homo- and γ-heterocoupling reactions. In the majority of examples presented, only a single stereoisomer was formed.Entities:
Keywords: asymmetric catalysis; organocatalysis; oxidative coupling; single-electron transfer; synthetic methods
Year: 2018 PMID: 29265675 DOI: 10.1002/anie.201711944
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336