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2,2 ' and 6,6 ' - four substitution amino phosphine ligands and its synthetic method

机译:2,2'和6,6'-四取代氨基膦配体及其合成方法

摘要

This invention, 2,2 '' and 6,6 '' relates to the - four substitution amino phosphine ligands and its synthetic method. Skeletal structure of the ligand is shown on description below. This ligand, using 2,6 jinitorokurorobenzen this the coupling doing and as the starting raw materials, 2,2 '' and 6,6 '' the second step which obtains - tetra- amino biphenyl and, 2,2 '' and 6,6 '' reacting - tetra- amino biphenyl and phosphine halide 2,2 '' and 6,6 '' first step and 2,2 '' and 6,6 '' by adding hydrogen to - tetra- nitro biphenyl palladium/the carbon which obtain - tetra- nitro biphenyl under existing, 2,2 '' and 6,6 '' it is produced with the method of including with the third step which obtains - four substitution amino phosphine. The ligand itself of this invention akiraru is chemical compound, it is something whose synthetic method of that ligand is simple. This ligand is converted to the kiraru catalyst of bimetaru of single konhuigureshiyon by finally introducing kiraritei from outside. This ligand used the metal catalyst, it is used by the asymmetrical reaction of many types, possesses high reaction activity and stereoselectivity.
机译:2,2''和6,6''本发明涉及-四个取代的氨基膦配体及其合成方法。配体的骨架结构显示在下面的描述中。该配体,使用2,6 jinitorokurorobenzen进行偶联,并以起始原料2,2''和6,6''作为第二原料,得到-四氨基联苯和2,2''和6,通过将氢加到-四硝基联苯钯/碳中,使6''反应-四氨基联苯和卤化膦2,2''和6,6''第一步以及2,2''和6,6''其通过在存在的2,2''和6,6''下获得-四硝基联苯的方法,是通过包括获得第四取代氨基膦的第三步骤的方法来制备的。本发明akiraru的配体本身是化合物,该配体的合成方法简单。通过最终从外部引入kiraritei,该配体被转化为单一konhuigureshiyon的双金属的kiraru催化剂。该配体用作金属催化剂,可用于多种类型的不对称反应,具有较高的反应活性和立体选择性。

著录项

  • 公开/公告号JP2010500295A

    专利类型

  • 公开/公告日2010-01-07

    原文格式PDF

  • 申请/专利权人 上海交通大学;

    申请/专利号JP20090523140

  • 发明设计人 張 万斌;謝 芳;房 芳;

    申请日2007-08-10

  • 分类号C07F9/46;

  • 国家 JP

  • 入库时间 2022-08-21 18:58:54

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