Spiro-Josiphos Ligands for the Ir-Catalyzed Asymmetric Synthesis of Chiral Amines under Hydrogenation Conditions.
Bin LiGang ZhouDongxu ZhangLin YaoMuqiong LiGuidong YangShengyong ZhangHuifang NiePublished in: Organic letters (2024)
Transition metal-catalyzed asymmetric hydrogenation possesses unparalleled advantages to prepare chiral amines. Here we reported a novel ligand that combined Josiphos and a spirobiindane scaffold and simultaneously investigated its application in Ir-catalyzed asymmetric hydrogenation for the synthesis of chiral amines. Excellent catalytic activity (5000 TON), high enantioselectivity (up to 99% ee ), and broad substrate scope (different C═N substrates) make it highly promising for both academic research and industrial applications.