Diverse Approaches for Enantioselective C−H Functionalization Reactions Using Group 9 Cp<sup>x</sup>M<sup>III</sup> Catalysts
Tatsuhiko Yoshino, Shun Satake, Shigeki Matsunaga
Abstract
Abstract Transition‐metal‐catalyzed C−H functionalization reactions with Cp*M III catalysts (M=Co, Rh, Ir) have found a wide variety of applications in organic synthesis. Albeit the intrinsic difficulties in achieving catalytic stereocontrol using these catalysts due to their lack of additional coordination sites for external chiral ligands and the conformational flexibility of the Cp ligand, catalytic enantioselective C−H functionalization reactions using the Group 9 metal triad with Cp‐type ligands have been intensively studied since 2012. In this minireview, the progress in these reactions according to the type of the chiral catalyst used are summarized and discussed. The development of chiral Cp x ligands the metal complexes thereof, artificial metalloenzymes, chiral carboxylate‐assisted enantioselective C−H activations, enantioselective alkylations assisted by chiral carboxylic acids or chiral sulfonates, and chiral transient directing groups are discussed.