Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones

Meng Lin Ma Zong Hai Peng Yu Guo Li Chen Hua Chen Xian Jun Li

引用本文: Meng Lin Ma,  Zong Hai Peng,  Yu Guo,  Li Chen,  Hua Chen,  Xian Jun Li. Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones[J]. Chinese Chemical Letters, 2010, 21(5): 576-579. doi: 10.1016/j.cclet.2010.01.030 shu
Citation:  Meng Lin Ma,  Zong Hai Peng,  Yu Guo,  Li Chen,  Hua Chen,  Xian Jun Li. Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones[J]. Chinese Chemical Letters, 2010, 21(5): 576-579. doi: 10.1016/j.cclet.2010.01.030 shu

Alkoxy substituted MeO-BIPHEP-type diphosphines ligands for asymmetric hydrogenation of aryl ketones

  • 基金项目:

    We thank the NSFC (No. 20272037), the Doctor's Foundation of Education Ministry of China (No. 20030610022) and 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 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.

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  • 收稿日期:  2009-10-09
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