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BINAPHTHOL DERIVATIVE AND OPTICALLY ACTIVE BINAPHTHOL METAL COMPLEX CATALYST USING THE SAME
BINAPHTHOL DERIVATIVE AND OPTICALLY ACTIVE BINAPHTHOL METAL COMPLEX CATALYST USING THE SAME
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机译:使用相同的联萘衍生物和光学活性联萘金属络合物催化剂
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摘要
PROBLEM TO BE SOLVED: To provide an optically active binaphthol metal complex catalyst for attaining satisfiable chemical yield and optical yield in the asymmetric nitroaldol reaction between a straight-chain aldehyde and nitromethane which has been inefficient for conventional such catalysts, and to provide a binaphthol derivative for preparing the catalyst.;SOLUTION: The binaphthol derivative is represented by general formula(1r) or (1s). An optical activator or binaphthol rare earth metal complex as the catalyst is also provided. In general formulas(1r) and (1s), R1 is a 1-6C alkyl, 2-6C alkenyl, 7-20C aralkyl or a chain substituent containing 1-3 heteroatoms in a 1-6C alkyl group; R2 is H, a halogen atom, 1-6C alkyl or 1-7C alkoxy group.;COPYRIGHT: (C)2005,JPO&NCIPI
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机译:解决的问题:提供一种光学活性的联萘酚金属络合物催化剂,以在直链醛与硝基甲烷之间的不对称硝基醛醇反应中获得令人满意的化学产率和光学产率,而该方法对于常规的此类催化剂而言效率低下,并提供联萘酚衍生物溶液:联萘酚衍生物由通式(1r)或(1s)表示。还提供了光活化剂或联萘酚稀土金属配合物作为催化剂。在通式(1r)和(1s)中,R 1 Sup>是1-6C烷基,2-6C烯基,7-20C芳烷基或在1-6C中含有1-3个杂原子的链取代基烷基; R 2 Sup>为H,卤原子,1-6C烷基或1-7C烷氧基。;版权:(C)2005,JPO&NCIPI
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