Two mechanistic pathways, that is, electrocyclization and electrophilic aromatic substitution, are operative in most intramolecular C-H amination reactions proceeding by metal nitrenoid catalysis. Reported here is an alternative mechanistic scaffold leading to benzofused δ-lactams selectively. Integrated experimental and computational analysis revealed that the reaction proceeds by a key spirocyclization step followed by a skeletal rearrangement. Based on this mechanistic insight, a new synthetic route to spirolactams has been developed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.201808892 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!