Transition metal π-arene complexes enable the dearomatization of benzene rings to access diversified unsaturated carbocycles through multistep synthetic procedures involving sequential addition of nucleophiles and electrophiles. This work details a single-step dearomatization process by reaction of Ru(η-arene) complexes with enolates derived from α-halo or α-(tosyloxy)esters to directly transform π-coordinated arenes to ring-expanded cycloheptatrienes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202421608 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!