| Literature DB >> 29271101 |
Kenneth Virgel N Esguerra1, Jean-Philip Lumb1.
Abstract
We describe a selective aerobic oxidation of meta-biaryl phenols that enables rapid access to functionalized phenanthrenes. Aerobic oxidations attract interest due to their efficiency, but remain underutilized in complex molecule settings due to challenges of selectivity. We discuss these issues in the context of Cu catalysis, and highlight the advantages of confining oxygen activation and substrate oxidation to the catalyst's inner-coordination sphere. This gives rise to predictable selectivity that we use for a concise synthesis of the aporphine dehydronornuciferine.Entities:
Keywords: aerobic copper catalysis; aerobic dehydrogenation; aporphine; phenol oxidation; quinone
Year: 2018 PMID: 29271101 DOI: 10.1002/anie.201710271
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336