A new C-2-symmetric diamine/diphosphine Ruthenium (II) complex, RuCl2P2N2H4, was used as an excellent catalyst to carry out the catalytic hydrogen transfer reduction of acetophenone. The conversion of acetophenone to ...A new C-2-symmetric diamine/diphosphine Ruthenium (II) complex, RuCl2P2N2H4, was used as an excellent catalyst to carry out the catalytic hydrogen transfer reduction of acetophenone. The conversion of acetophenone to 2-phenylethanol was up to 99% under the following reaction conditions: substrate:Ru:(CH3)(2)CHOK = 200:1:12; reaction temperature of 65 degrees C; reaction time of 2 h; normal pressure. A hydride transfer mechanism was also discussed.展开更多
Novel chiral tetraaza ligands（R）-N,N′-bis[2-（piperidin-1-yl）benzylidene]propane-l,2-diamine 6 and（S）-N-[2-（piperidin-l- yl）benzylidene]-3-{[2-（piperidin-1-yl）benzylidene]amino}-alanine sodium salt 7 have be...Novel chiral tetraaza ligands（R）-N,N′-bis[2-（piperidin-1-yl）benzylidene]propane-l,2-diamine 6 and（S）-N-[2-（piperidin-l- yl）benzylidene]-3-{[2-（piperidin-1-yl）benzylidene]amino}-alanine sodium salt 7 have been synthesized and fully characterized by NMR,IR,MS and CD spectra.The catalytic property of the ligands was investigated in Ir-catalyzed enantioselective transfer hydrogenation of ketones.The corresponding optical active alcohols were obtained with high yields and moderate ees under mild reaction conditions.展开更多
文摘A new C-2-symmetric diamine/diphosphine Ruthenium (II) complex, RuCl2P2N2H4, was used as an excellent catalyst to carry out the catalytic hydrogen transfer reduction of acetophenone. The conversion of acetophenone to 2-phenylethanol was up to 99% under the following reaction conditions: substrate:Ru:(CH3)(2)CHOK = 200:1:12; reaction temperature of 65 degrees C; reaction time of 2 h; normal pressure. A hydride transfer mechanism was also discussed.
基金the National Natural Science Foundation of China(No21173176)the Natural Science Foundation of Guangxi Province of China(No0991016)for the financial support of this work
文摘新 polydentate mixed-N， P， O chiral ligands 被二度(o-formylphenyl ) 的冷凝作用综合了在 CHCl3 的 -phenylphosphane 和 R-phenylglycinol，并且充分由红外， NMR 和 EIMS 系列描绘了。这些 ligands 为酉同类的不对称的转移加氢作为催化系统与简单 Ni 复杂 Ni (PPhs ) 2Cl2in situ 被采用，并且相应光白酒在温和条件下面与多达 84% ee 被获得。
基金the National Natural Science Foundation of China(Nos.20423002,20923004,and 21173176)Program for Changjiang Scholars and Innovative Research Team in University(No.IRT1036)State Key Laboratory of Physical Chemistry of Solid Surfaces for financial support
文摘Novel chiral tetraaza ligands（R）-N,N′-bis[2-（piperidin-1-yl）benzylidene]propane-l,2-diamine 6 and（S）-N-[2-（piperidin-l- yl）benzylidene]-3-{[2-（piperidin-1-yl）benzylidene]amino}-alanine sodium salt 7 have been synthesized and fully characterized by NMR,IR,MS and CD spectra.The catalytic property of the ligands was investigated in Ir-catalyzed enantioselective transfer hydrogenation of ketones.The corresponding optical active alcohols were obtained with high yields and moderate ees under mild reaction conditions.
