首页> 外国专利> METHOD OF ENANTIOMETRICALLY SELECTIVE NUCLEOPHILIC ADDITION REACTION TO CARBONYL OF ENAMIDE AND METHOD OF SYNTHESIZING OPTICALLY ACTIVE ALPHA-HYDROXY-GAMMA-KETO ACID ESTER AND HYDROXYDIKETONE

METHOD OF ENANTIOMETRICALLY SELECTIVE NUCLEOPHILIC ADDITION REACTION TO CARBONYL OF ENAMIDE AND METHOD OF SYNTHESIZING OPTICALLY ACTIVE ALPHA-HYDROXY-GAMMA-KETO ACID ESTER AND HYDROXYDIKETONE

机译:对映异构体对烯酰胺羰基的选择性亲核加成反应的方法以及合成光学活性的α-羟基-γ-酮酸和羟基二酮的方法

摘要

A method of an enantioselective nucleophilic addition reaction to carbonyl, which enables an asymmetric synthesis of an optically active α-hydroxy-γ-keto acid ester, an optically active α-hydroxy-γ-amino acid ester, hydroxydiketone compounds, etc. being useful as a raw material or synthesis intermediate for producing a pharmaceutical preparation, an agricultural chemical, a fragrance, a functional polymer or the like. In this method, the nucleophilic addition reaction of enamide compound accompanied by hydroxyl (-OH) formation to carbonyl is carried out in the presence of a chiral catalyst with copper or nickel.
机译:一种对羰基的对映选择性亲核加成反应的方法,该方法能够不对称地合成旋光性α-羟基-γ-酮酸酯,旋光性α-羟基-γ-氨基酸酯,羟基二酮化合物等可用作生产药物制剂,农药,香料,功能聚合物等的原料或合成中间体。在这种方法中,在铜或镍的手性催化剂存在下,烯酰胺化合物的亲核加成反应伴随着羟基(-OH)形成为羰基。

著录项

  • 公开/公告号EP1707556A4

    专利类型

  • 公开/公告日2007-11-21

    原文格式PDF

  • 申请/专利权人 JAPAN SCIENCE AND TECHNOLOGY AGENCY;

    申请/专利号EP20050704278

  • 发明设计人 KOBAYASHI SHU;

    申请日2005-01-24

  • 分类号C07C67/343;C07B53/00;C07B61/00;C07C69/738;C07C269/04;C07C271/22;C07D207/18;C07D307/32;C07F7/18;

  • 国家 EP

  • 入库时间 2022-08-21 20:00:42

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