Selectivity in the Aerobic Dearomatization of Phenols: Total Synthesis of Dehydronornuciferine by Chemo- and Regioselective Oxidation.

Angew Chem Int Ed Engl

Department of Chemistry, McGill University, 801 Sherbrooke St. W., Montreal, Quebec, H3A 0B8, Canada.

Published: February 2018

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.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201710271DOI Listing

Publication Analysis

Top Keywords

selectivity aerobic
4
aerobic dearomatization
4
dearomatization phenols
4
phenols total
4
total synthesis
4
synthesis dehydronornuciferine
4
dehydronornuciferine chemo-
4
chemo- regioselective
4
regioselective oxidation
4
oxidation describe
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!