首页> 外国专利> CINCHONA ALKALOID CATALYST FOR HETEROGENEOUS ASYMMETRIC AMINOHYDROXYLATION OF OLEFINS

CINCHONA ALKALOID CATALYST FOR HETEROGENEOUS ASYMMETRIC AMINOHYDROXYLATION OF OLEFINS

机译:五倍子烷基碱催化烯烃非均相不对称氨氧化

摘要

PURPOSE: A process for preparing an optical active aminoalcohol compound using a cinchona alkaloid catalyst having excellent catalytic performance, reusable and excellent in thermal, mechanical stability, a nitrogen source and a base is provided which carries out the heterogeneous asymmetric aminohydroxylation of olefins economically and can improve processing difficulties by high toxicity and volatility of OsO4. CONSTITUTION: In the process for manufacturing an optical active aminoalcohol compound by heterogeneous asymmetric aminohydroxylation of olefins, the process uses a catalytic system containing conventional cinchona alkaloids of formula 1 and a nitrogen source and a base. In formula, Y is hydroquinidinyl represented by formula 2 or hydroquinidinyl represented by formula 3, X represents an unsaturated compound containing 0 or 4 carbons, pyridazine in case X is 0 and phthalazine in case X is an unsaturated compound, R represents methoxy, ethoxy or methyl.
机译:用途:提供一种使用金鸡纳生物碱催化剂制备旋光性氨基醇化合物的方法,该催化剂具有优异的催化性能,可重复使用且在热,机械稳定性方面极佳,并提供氮源和碱,可以经济地进行烯烃的异质不对称氨基羟基化反应,并且可以通过OsO4的高毒性和挥发性来改善加工难度。组成:在通过烯烃的非均相不对称氨基羟基化生产旋光性氨基醇化合物的方法中,该方法使用的催化体系包含常规的式1金鸡纳生物碱以及氮源和碱。式中,Y为式2所示的氢醌基或式3所示的氢醌基,X为碳数为0或4的不饱和化合物,X为0时为哒嗪,X为不饱和化合物时为酞嗪,R为甲氧基,乙氧基或甲基。

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