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    • 5. 发明授权
    • Methylcyclohexyl-O-anisylphosphine
    • 甲基环己基-O-茴香醚
    • US4294989A
    • 1981-10-13
    • US939568
    • 1978-09-05
    • William S. KnowlesMilton J. Sabacky
    • William S. KnowlesMilton J. Sabacky
    • B01J31/18B01J31/24C07F9/32C07F9/34C07F9/40C07F9/50C07F9/53C07F9/70
    • C07F9/70B01J31/1875B01J31/2404C07F9/32C07F9/34C07F9/40C07F9/50C07F9/53B01J2231/645B01J2531/822
    • Process for the homogeneous catalytic hydrogenation of .beta.-substituted-.alpha.-acylamido-acrylic acids which yields, after hydrogenation, an optically active mixture. The process comprises the hydrogenation of .beta.-substituted-.alpha.-acylamido-acrylic acids in the presence of an optically active coordinated metal complex hydrogenation catalyst, in which the metal is selected from the group consisting of rhodium, iridium, ruthenium, osmium, palladium and platinum.This process is a generalized process for any asymmetric hydrogenation of .beta.-substituted-.alpha.-acylamido-acrylic acids in which one .alpha.-amino acid enantiomorph is the desired end-product. It is especially useful for the preparation of .alpha.-amino acids found in nature which possess optical activity and which have a hydrogen attached to the asymmetric center.This invention also relates to new optically active coordinated metal complex hydrogenation catalysts.
    • β-取代-α-酰氨基 - 丙烯酸均相催化氢化的方法,其在氢化后产生光学活性混合物。 该方法包括在光学活性配位金属络合物氢化催化剂存在下β-取代-α-酰氨基丙烯酸的氢化,其中金属选自铑,铱,钌,锇,钯和 铂。 该方法是用于β-取代-α-酰氨基 - 丙烯酸的任何不对称氢化的通用方法,其中一个α-氨基酸对映体是所需的最终产物。 特别适用于制备具有光学活性且具有附着于不对称中心的氢的自然界中发现的α-氨基酸。 本发明还涉及新的光学活性配位金属络合物氢化催化剂。