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.201808892DOI Listing

Publication Analysis

Top Keywords

revisiting arene
4
arene csp
4
csp amidation
4
amidation intramolecular
4
intramolecular transfer
4
transfer iridium
4
iridium nitrenoids
4
nitrenoids evidence
4
evidence spirocyclization
4
spirocyclization pathway
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!