Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones
摘要:
In this paper, a series of optically active MeO-BIPHEP-type ligands, (S)-6,6'-dimethoxy-2,2'-bis(di-p-alkoxyphenylphosphine)-1,1'-biphenyl were synthesized and used to prepare the ruthenium complex. The effects of para-substituted were observed, the results showed that the ruthenium catalysts [diphosphine RuCl2 diamine] containing both t-Bu and i-Pr substitutions have better activities and enantioselectivities than the non-substituted ruthenium catalysts in the asymmetric hydrogenation of acetophenone (C) 2010 Hua Chen Published by Elsevier B V. on behalf of Chinese Chemical Society All rights reserved
synthesized and used in the copper(I)-catalyzed enatioselective [3 + 2] cycloaddition of iminoesters with alkenes. A variety of highly functionalized pyrrolidines were obtained in excellent yield and enatioselectivity. This is the first example of a pair of P-stereogenic ligands working as pseudoenantiomers to tune the enantio- and diastereoselective 1,3-dipolar cycloaddition, and providing a pair of