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首页> 外文期刊>Synlett >Development of new asymmetric reactions utilizing tartaric acid esters as chiral auxiliaries. The design of an efficient chiral multinucleating system
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Development of new asymmetric reactions utilizing tartaric acid esters as chiral auxiliaries. The design of an efficient chiral multinucleating system

机译:利用酒石酸酯作为手性助剂开发新的不对称反应。高效手性多核系统的设计

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摘要

A practical method for the construction of chiral molecules has been designed using a novel strategy based on systems possessing multiple metal centers and tartaric acid esters as chiral auxiliaries. By using this design, we have developed methods for carrying out highly enantioselective (1) Simmons-Smith reaction, (2) 1,3-dipolar cycloaddition reactions of nitrile oxides and nitrones, and (3) nucleophilic additions of organometallic compounds to imine derivatives. [References: 90]
机译:基于具有多个金属中心和酒石酸酯作为手性助剂的系统,已经使用一种新颖的策略设计了一种用于构建手性分子的实用方法。通过这种设计,我们开发了进行高对映选择性的方法(1)Simmons-Smith反应,(2)腈和硝酮的1,3-偶极环加成反应,以及(3)有机金属化合物与亚胺衍生物的亲核加成。 [参考:90]

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