本论文在查阅相关资料基础上综述了不对称催化还原反应研究新进展。
This paper summarizes the new progress of the asymmetric catalytic reduction reaction on the basis of relevant references.
手性胺化合物广泛存在于自然界中并扮演着重要的角色，亚胺的不对称催化还原反应是制备手性胺化合物的最直接有效的方法。
Chiral amines widely existed and play an important role in the nature. Catalytic asymmetric reduction of imines represents one of the most important methods for preparing chiral amines.
本文综述了应用手性高分子试剂和催化剂对潜手性化合物通过不对称氧化、还原、烷基化、加成反应进行不对称合成的进展情况。
This review deals with the recent progress in asymmetric synthesis using chiral polymeric reagents and catalysts for oxidation, reduction, alkylation and addition of prochiral compounds.
结合非水相生物催化的优势利用微生物细胞催化不对称还原羰基化合物可以有效地制备这些手性醇。
Combining the advantages of biocatalysis in nonaqueous media, asymmetric reduction of corresponding carbonyl compounds using microbial cells is an efficient method to produce these chiral alcohols.
对面包酵母水相催化不对称还原opbe进行研究。
The asymmetric reduction of OPBE catalyzed by Baker Yeast in water medium to synthesis HPBE was investigated.
生物催化的还原反应能使分子内的羰基或碳-碳双键立体选择性的还原，将潜手性底物转化为手性产物，在不对称合成中有着重要的作用。
Biocatalytic reduction of the carbonyl groups or the carbon-carbon double bonds of the compounds has been utilized as a method for transforming the prochiral substrate into chiral product.
不对称催化硼氢化反应是应用广泛且具有工业价值的反应，其中的硼烷还原前手性酮反应有着举足轻重的作用。
Asymmetric hydroboration is a kind of widely applied and valuable reaction, in which borane reduction of prochiral ketones reaction is an important method.
手性醇是药物合成的重要手性砌块，利用生物催化剂不对称还原羰基化合物是手性醇制备的重要方法。
Chiral alcohols are important building blocks for drug synthesis. The asymmetric reduction of carbonyl compounds with biocatalysts is an important method for producing chiral alcohols.
手性醇是药物合成的重要手性砌块，利用生物催化剂不对称还原羰基化合物是手性醇制备的重要方法。
Chiral alcohols are important building blocks for drug synthesis. The asymmetric reduction of carbonyl compounds with biocatalysts is an important method for producing chiral alcohols.
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