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高效立体选择性构建双螺[恶唑烷-2-硫酮]双吲哚啉和双螺[咪唑烷-2-硫酮]双吲哚啉。

Highly efficient and stereoselective construction of dispiro-[oxazolidine-2-thione]bisoxindoles and dispiro[imidazolidine-2-thione]bisoxindoles.

机构信息

National Engineering Research Center of Chiral Drugs, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China.

出版信息

Org Lett. 2012 Jan 20;14(2):490-3. doi: 10.1021/ol203081x. Epub 2012 Jan 11.

Abstract

An efficient and stereoselective reaction between 3-isothiocyanato oxindoles and isatins/isatinimines has been developed to afford structurally diverse dispiro[oxazolidine-2-thione]bisoxindoles and dispiro[imidazolidine-2-thione]bisoxindoles in excellent results under mild conditions. The potential of asymmetric induction by means of a chiral auxiliary was explored. The isomers are separable, and products could be isolated as single diastereomers by column chromatography. Further synthetic transformations of the reaction product were also successfully realized.

摘要

一种高效、立体选择性的 3-异硫氰酸基氧化吲哚和色酮/异吲哚啉反应,可以在温和条件下以优异的结果得到结构多样的双螺[氧杂环戊烷-2-硫酮]双氧化吲哚和双螺[咪唑烷-2-硫酮]双氧化吲哚。通过手性辅助手段探索了不对称诱导的潜力。异构体是可分离的,产物可以通过柱层析作为单一非对映异构体分离。反应产物的进一步合成转化也成功实现。

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