首页> 外国专利> Optics using a chiral metal complex consisting of an amino acid compound and an axial asymmetric N-(2-acylaryl)-2-5,7-dihydro-6H-dibenzo c, e azepin-6-yl acetamide compound Method for synthesizing active -amino acid

Optics using a chiral metal complex consisting of an amino acid compound and an axial asymmetric N-(2-acylaryl)-2-5,7-dihydro-6H-dibenzo c, e azepin-6-yl acetamide compound Method for synthesizing active -amino acid

机译:使用由氨基酸化合物和轴向不对称N-(2-酰基芳基)-2- [5,7-二氢-6H-二苯并[c,e] azepin-6-基]乙酰胺化合物组成的手性金属配合物的光学方法用于合成活性氨基酸

摘要

Objects of the present invention are to provide an industrially applicable method for producing an optically active ±-amino acid in high yield and in a highly enantioselective manner, to provide a simple production method of an optically active ±,±-disubstituted ±-amino acid, and to provide an intermediate useful for the above production methods of an optically active ±-amino acid and an optically active ±,±-disubstituted ±-amino acid. The present invention provides a production method of an optically active ±-amino acid or a salt thereof, the production method comprising introducing a substituent into the ± carbon in the ±-amino acid moiety of a metal complex represented by the following Formula (1): by an alkylation reaction, an aldol reaction, the Michael reaction, or the Mannich reaction, and releasing an optically pure ±-amino acid enantiomer or a salt thereof by acid decomposition of the metal complex.
机译:本发明的目的是提供一种以高收率和高对映选择性的方式生产旋光性±氨基酸的工业适用方法,以提供一种旋光性±,±二取代的±氨基酸的简单生产方法。 ,并提供可用于上述旋光性±氨基酸和旋光性±,±二取代±氨基酸的中间体。本发明提供旋光性±氨基酸或其盐的制备方法,该制备方法包括将取代基引入由下式(1)表示的金属络合物的±氨基酸部分的±碳中。 :通过烷基化反应,醛醇缩合反应,迈克尔反应或曼尼希反应,并通过金属配合物的酸分解释放出光学纯的±氨基酸对映体或其盐。

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