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Manufacturing method null of optical active ant - ru acetic acid

机译:光学活性剂钌乙酸的制造方法无效

摘要

PURPOSE:To obtain the aimed compound in good conversion rate and optical yield, by using a metallic catalyst modified with a specific optically active metallocenylphosphine derivative in producing the titled compound from the corresponding olefin derivative by an asymmetric hydrogen reduction method. CONSTITUTION:A compound expressed by formula I (Ar is formula II or III; R4-R4 are H, lower alkyl or phenyl or further R3 and R4 are halogen, lower alkoxy, etc.) is asymmetrically reduced with hydrogen in the presence of a metallic catalyst modified with an optically active metallocenylphosphine derivative expressed by formula IV (X is CH2, O or NR9; Z is alkylene, CO, COCH2 or CH2CO; Y is OR10 or NR11R12; R5 and R6 are lower alkyl, 5-8C cycloalkyl, aryl, etc.; R7-R12 are H, lower alkyl or NR11R12 which may form a heterocyclic ring; M is Fe, Ru or Os; n is 0 or 1) to advantageously obtain the aimed compound expressed by formula V useful as an intermediate for medicines.agricultural chemicals, etc., in a desired steric configuration. Furthermore, the steric configuration of the aimed compound can be controlled by changing the steric coordination of the catalyst used.
机译:目的:在不对称氢还原法从相应的烯烃衍生物生产标题化合物的过程中,通过使用经特定旋光性金属茂金属膦衍生物改性的金属催化剂,以良好的转化率和光学收率获得目标化合物。组成:由式I表示的化合物(Ar为式II或III; R4-R4为H,低级烷基或苯基或另外的R3和R4为卤素,低级烷氧基等)在存在下的情况下被氢不对称还原用式IV表示的旋光金属茂基膦衍生物改性的金属催化剂(X为CH2,O或NR9; Z为亚烷基,CO,COCH2或CH2CO; Y为OR10或NR11R12; R5和R6为低级烷基,5-8C环烷基,芳基等; R 7 -R 12为H,可形成杂环的低级烷基或NR 11 R 12; M为Fe,Ru或Os; n为0或1)以有利地获得由式V表示的目标化合物,用作中间体以所需的空间构型用于药品,农业化学品等。此外,可以通过改变所用催化剂的空间配位来控制目标化合物的空间构型。

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