Herein, we report a chiral phosphine-triazole ligand for the Ir-catalyzed asymmetric hydrogenation of exocyclic benzofused alkenes. Overcoming previous limitations, the catalytic system is able to successfully hydrogenate exocyclic olefins bearing a benzofused five- and six-membered ring motif (ee’s between 92 to 99%). The catalyst tolerates well the presence of several substituents and substitution patterns at both aromatic rings. The absence of a competing isomerization process together with the perfect fit of the olefins in the catalyst chiral pocket are key to surpass the previous limitations in the hydrogenation of both 5- and 6-membered ring benzofused exocyclic olefins.
Biosca, M.; de la Cruz-Sánchez, P.; Tarr, D.; Llanes, P.; Karlsson, E. A.; Margalef, J.; Pàmies, O.; Pericàs, M. A.; Diéguez, M.
Adv. Synth. Catal. 2022, 365 (2), 167-177
DOI:
10.1002/adsc.202200870
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