METHOD OF ENANTHIO-SELECTIVE NUCLEOPHILIC ADDITION REACTION FOR CONVERSION OF ENAMIDE TO IMINE AND METHOD OF SYNTHESIZING ALPHA AMINO-GAMMA-KETO ACID ESTER
    25.
    发明公开
    METHOD OF ENANTHIO-SELECTIVE NUCLEOPHILIC ADDITION REACTION FOR CONVERSION OF ENAMIDE TO IMINE AND METHOD OF SYNTHESIZING ALPHA AMINO-GAMMA-KETO ACID ESTER 有权
    过程用于对映选择性亲核加成甲烯酰胺送至MIN AND METHOD FOR SYNTHESIS OF ALPHA氨基-γ-酮酸酯

    公开(公告)号:EP1707559A1

    公开(公告)日:2006-10-04

    申请号:EP05704279.8

    申请日:2005-01-24

    Inventor: KOBAYASHI, Shu

    Abstract: An asymmetric synthesis of amino acid compound that is useful as a starting material or synthetic intermediate for production of medicinal products, agrichemicals, perfumes, functional polymers, etc. There is provided a method of enanthio-selective nucleophilic addition reaction to imine compound being a method of nucleophilic addition reaction of enamide compound accompanied by amino formation to imino group (-CH=N-) of imine compound, characterized in that the reaction is performed in the presence of a chiral copper catalyst. Further, there is provided a novel method of synthesizing an amino acid compound, etc., to which the above is applied.

    Abstract translation: 确实氨基酸化合物的不对称合成是作为起始材料是有用的或合成中间体生产医药产品,农用化学品,香料,功能性聚合物等的本发明提供enanthio选择性亲核加成反应来亚胺化合物的方法是一个方法 由氨基形成的陪同下,以亚氨基亚胺化合物的基团(-CH = N-)化合物的烯酰胺亲核加成反应的,在DASS特点死反应在手性铜催化剂的存在下进行。 此外,提供了一种合成的氨基酸化合物等的一种新颖的方法,向其中上述被应用。

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