669091-00-3Relevant academic research and scientific papers
Phosphino hydrazones as suitable ligands in the asymmetric Suzuki-Miyaura cross-coupling
Ros, Abel,Estepa, Beatriz,Bermejo, Antonio,Alvarez, Eleuterio,Fernandez, Rosario,Lassaletta, Jose M.
experimental part, p. 4740 - 4750 (2012/07/02)
Phosphino hydrazones derived from C2-symmetric hydrazines exhibit excellent catalytic activity and provide good enantioselectivities in the asymmetric Suzuki-Miyaura cross-coupling to axially chiral biaryls, in particular for the most challenging reactions of monocyclic, functionalized aryl bromides and triflates. X-ray analysis of preformed [Pd(P/N)Cl2] precatalysts [(P/N) = phosphino hydrazone] revealed a strong n-π conjugation in the hydrazone moiety, identified by a high planarity degree at the pyrrolidine N(sp3) atom, that makes rotations around N-N bonds inconsequential. The complexes are also characterized by an envelope-like conformation with the Pd atom placed at the opposite side to the 2-phenyl group on the nearest stereogenic center of the pyrrolidine group. The isolation and structural analysis of oxidative addition intermediates indicate that the configurational stability of Pd-C(Ar) bonds is dependent on the substitution pattern in the aryl bromide.
Application of P,N-Sulfinyl Imine Ligands to Iridium-Catalyzed Asymmetric Hydrogenation of Olefins
Schenkel, Laurie B.,Ellman, Jonathan A.
, p. 1800 - 1802 (2007/10/03)
The utility of a novel class of P,N-ligands incorporating a chiral sulfinyl imine moiety is demonstrated in the iridium-catalyzed hydrogenation of both functionalized and unfunctionalized olefins, in which enantioselectivities of up to 94% are achieved. T
