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作 者:Meng Lin Ma Zong Hai Peng Yu Guo Li Chen Hua Chen Xian Jun Li
机构地区:[1]Department of Chemistry,Xihua University,Chengdu 610039,China [2]Key Lab of Green Chemistry and Technology,Ministry of Education,The Institute of Homogeneous Catalysis,Faculty of Chemistry,Sichuan University,Chengdu 610064,China
出 处:《Chinese Chemical Letters》2010年第5期576-579,共4页中国化学快报(英文版)
基 金:the NSFC(No.20272037),the Doctor's Foundation of Education Ministry of China(No.20030610022);Foundation of Xihua University(No.R0723315) and(No.07ZA109) for the financial support of this work.
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 RuCl;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.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 RuCl<sub>2</sub> 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.
关 键 词:Aryl ketone Asymmetric hydrogenation Biaryl phosphines ligands Ruthenium complex
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