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铁(II)基金属自由基活化:从传统点击化学到脱氮环化反应的转变。

Iron(II)-Based Metalloradical Activation: Switch from Traditional Click Chemistry to Denitrogenative Annulation.

机构信息

Division of Molecular Synthesis & Drug Discovery, Centre of Bio-Medical Research (CBMR), SGPGIMS Campus, Raebareli Road, Lucknow, 226014, U.P., India.

出版信息

Angew Chem Int Ed Engl. 2019 Aug 12;58(33):11439-11443. doi: 10.1002/anie.201904702. Epub 2019 Jul 3.

Abstract

A unique concept for the intermolecular denitrogenative annulation of 1,2,3,4-tetrazoles and alkynes was discovered by using a catalytic amount of Fe(TPP)Cl and Zn dust. The reaction precludes the traditional, more favored click reaction between an organic azide and alkynes, and instead proceeds by an unprecedented metalloradical activation. The method is anticipated to advance access to the construction of important basic nitrogen heterocycles, which will in turn enable discoveries of new drug candidates.

摘要

通过使用催化量的 Fe(TPP)Cl 和锌粉,发现了一种独特的概念,用于 1,2,3,4-四唑和炔烃的分子间脱氮环化。该反应排除了传统的、更受欢迎的有机叠氮化物和炔烃之间的点击反应,而是通过前所未有的金属自由基活化进行。该方法有望促进构建重要的基本含氮杂环,这反过来又将能够发现新的药物候选物。

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