Tuning the Peri Effect for Enantioselectivity: Asymmetric Hydrogenation of Unfunctionalized Olefins with the BIPI Ligands

…, M Eriksson, JP Wu, N Grinberg, H Lee…

Index: Busacca, Carl A.; Qu, Bo; Gret, Nicole; Fandrick, Keith R.; Saha, Anjan K.; Marsini, Maurice; Reeves, Diana; Haddad, Nizar; Eriksson, Magnus; Wu, Jiang-Ping; Grinberg, Nelu; Lee, Heewon; Li, Zhibin; Lu, Bruce; Chen, Dajun; Hong, Yaping; Ma, Shengli; Senanayake, Chris H. Advanced Synthesis and Catalysis, 2013 , vol. 355, # 8 p. 1455 - 1463

Full Text: HTML

Citation Number: 7

Abstract

Abstract The modular nature of the BIPI ligands allows for systematic optimization of each ligand region. The development of ligands optimized for asymmetric hydrogenation of the challenging unfunctionalized olefin substrate class is described. The naphthyl peri position, C-8, has been identified as a critical stereocontrol element in the design of these ligands. Highly enantioselective ligands suitable for hydrogenation of tri-and tetrasubstituted ...