首页 | 本学科首页   官方微博 | 高级检索  
     

苯乙胺衍生的手性膦-亚磷酰胺酯配体在Rh-催化a-烯醇酯膦酸酯的不对称氢化反应中的应用
引用本文:胡向平. 苯乙胺衍生的手性膦-亚磷酰胺酯配体在Rh-催化a-烯醇酯膦酸酯的不对称氢化反应中的应用[J]. 分子催化, 2012, 26(6): 487-492
作者姓名:胡向平
作者单位:中国科学院大连化学物理研究所
基金项目:The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan)
摘    要:将苯乙胺衍生的手性膦-亚磷酰胺酯配体应用在Rh-催化α-烯醇酯膦酸酯的不对称氢化反应中,考察了配体结构及反应条件对反应结果的影响,并在优化的条件下研究了各种底物的适用范围,产物的对映选择性最高>99%ee.

关 键 词:不对称催化    膦-亚磷酰胺酯配体  α-烯醇酯膦酸酯  氢化
收稿时间:2012-11-08
修稿时间:2012-12-01

Rh-Catalyzed Asymmetric Hydrogenation of a-Enol Ester Phosphonates with 1-Phenylethylamine-Derived Phosphine-Phosphoramidite Ligands
HU Juan,WANG Dao-yong,ZHENG Zhuo,HU Xiang-ping. Rh-Catalyzed Asymmetric Hydrogenation of a-Enol Ester Phosphonates with 1-Phenylethylamine-Derived Phosphine-Phosphoramidite Ligands[J]. Journal of Molecular Catalysis (China), 2012, 26(6): 487-492
Authors:HU Juan  WANG Dao-yong  ZHENG Zhuo  HU Xiang-ping
Affiliation:*(Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023,China)
Abstract:A series of phosphine-phosphoramidite ligands derived from commercially available, inexpensive chiral 1-phenylethylamine were employed in the Rh-catalyzed asymmetric hydrogenation of various a-enol ester phosphonates. The results indicated that the ligand (Sc,Sa)-2b bearing a Me-group on amino moiety exhibited similar enantioselectivity but superior catalytic activity to (Rc,Ra)-THNAPhos. Excellent enantioselectivities (up to >99% ee) and high catalytic activity (S/C up to 5000) have been achieved in the hydrogenation of various b-alkyl and b-aryl substituted substrates, demonstrating the high potential of this phosphine-phosphoramidite ligand in the preparation of optically active a-hydroxyphosphonates
Keywords:asymmetric catalysis   rhodium   phosphine-phosphoramidite ligand   a-enol ester phosphonate   hydrogenation
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《分子催化》浏览原始摘要信息
点击此处可从《分子催化》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号