RESUMO
Chiral cyclopentadienyl (Cp) rhodium(III) are powerful catalysts for achieving asymmetric C-H activation. This paper describes the design and synthesis of a new type of chiral Cp ligand bearing a chiral 3,3,3',3'-tetramethyl-1,1'-spirobiindanyl backbone. It features convenient synthesis, easy modification, and relatively low cost. Moreover, it holds great potential in achieving asymmetric C-H activation as exemplified by four examples examined in this work.
RESUMO
A new class of C2 -symmetric, chiral cyclopentadienyl ligand based on planar chiral ferrocene backbone was developed. A series of its corresponding rhodium(I), iridium(I), and ruthenium(II) complexes were prepared as well. In addition, the rhodium(I) complexes were evaluated in the asymmetric catalytic intramolecular amidoarylation of olefin-tethered benzamides via C-H activation.