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作 者:GONG Da-chun ZHOU Hua WEI Ping OUYANG Ping-kai
机构地区:[1]College of Chemistry and Life Science, China Three Gorges University, Yichang 443001, P. R. China [2]College of Life Science and Pharmacy, Nanfing University of Technology, Nanfing 210009, P. R. China
出 处:《Chemical Research in Chinese Universities》2007年第5期544-548,共5页高等学校化学研究(英文版)
基 金:Supported by the National Basic Research Program of China(No.2003CB716000).
摘 要:New ligand 1,2-bis{di[(R,R)-1,3,2-oxzaphosphlidine]phosphino}ethane [(R,R)-BDOPPEs 1,2,3 and 4] with C2-symmetric axis and bearing nitrogen and oxygen were synthesized from readily available optically active amino alcohols.Rh complexes with these ligands were highly enantioselective catalysts for asymmetric hydrogenation of N-benzoyldehydroamino acid derivatives and α-functionalized ketones in 99%e.e.and 98%e.e.,respectively.This new class of(R,R)-BDOPPEs 1,2,3 and 4 gave much more effectivity and enantionselectivity than their corresponding non-C2-asymmetric aminophosphine phosphinite.New ligand 1,2-bis{di[(R,R)-1,3,2-oxzaphosphlidine]phosphino}ethane [(R,R)-BDOPPEs 1,2,3 and 4] with C2-symmetric axis and bearing nitrogen and oxygen were synthesized from readily available optically active amino alcohols.Rh complexes with these ligands were highly enantioselective catalysts for asymmetric hydrogenation of N-benzoyldehydroamino acid derivatives and α-functionalized ketones in 99%e.e.and 98%e.e.,respectively.This new class of(R,R)-BDOPPEs 1,2,3 and 4 gave much more effectivity and enantionselectivity than their corresponding non-C2-asymmetric aminophosphine phosphinite.
关 键 词:(R R) -BDOPPE C2-Symmetry Asymmetric catalytic hydrogenation
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