A Stereodivergent–Convergent Chiral Induction Mode in Atroposelective Access to Biaryls via Rhodium-Catalyzed C–H Bond Activation

Abstract

Understanding the reaction mechanisms, particularly the chiral induction mode, is critical for the development of new asymmetric catalytic reactions. Rhodium­(III)-catalyzed C–H activation en route to atroposelective [4 + 2] annulative coupling with α-diazo β-ketoesters has been realized, affording axially chiral phenanthrenes in good to excellent enantioselectivity. A combination of experimental and computational studies revealed a nontraditional stereodivergent–convergent chiral induction mode. The reaction proceeded with a rhodafluorene intermediate, followed by competitive, constructive, and stereodivergent migratory insertions of the two Rh–C­(aryl) bonds into the carbene species to give β-ketoester intermediates. Then, the other Rh–C­(aryl) bond migratorily inserts into the ketone carbonyl group. Following this stereodetermining carbonyl insertion, an ester-chelated rhodium­(III) alkoxide species bearing two poorly controlled chiral centers and a well-controlled C­(sp2)–C­(sp3) chiral axis is generated. The final product is delivered via stereoconvergent elimination of a rhodium­(III) species with retention of the well-controlled axial chirality and with loss of the central chirality