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吡啶𬭩盐的合成及其在功能化联吡啶形成中的应用。

Synthesis of Pyridylsulfonium Salts and Their Application in the Formation of Functionalized Bipyridines.

机构信息

SSPC, the SFI Research Centre for Pharmaceuticals, Centre for Synthesis & Chemical Biology, UCD School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland.

出版信息

Org Lett. 2020 Nov 6;22(21):8451-8457. doi: 10.1021/acs.orglett.0c03048. Epub 2020 Oct 22.

Abstract

An S-selective arylation of pyridylsulfides with good functional group tolerance was developed. To demonstrate synthetic utility, the resulting pyridylsulfonium salts were used in a scalable transition-metal-free coupling protocol, yielding functionalized bipyridines with extensive functional group tolerance. This modular methodology permits selective introduction of functional groups from commercially available pyridyl halides, furnishing symmetrical and unsymmetrical 2,2'- and 2,3'-bipyridines. Iterative application of the methodology enabled the synthesis of a functionalized terpyridine with three different pyridine components.

摘要

发展了一种对吡啶基硫化物具有良好官能团耐受性的 S-选择性芳基化反应。为了展示合成的实用性,所得的吡啶𬭩盐被用于可规模化的无过渡金属的偶联反应中,得到了具有广泛官能团耐受性的功能化联吡啶。这种模块化方法可以选择性地从商业可得的吡啶卤化物中引入功能基团,从而提供对称和不对称的 2,2'-和 2,3'-联吡啶。该方法的迭代应用使具有三个不同吡啶基的功能化三联吡啶的合成成为可能。

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