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钯(II)催化的酰胺γ-C(sp)-H 炔基化反应:酰胺 RC(O)NHR 的 R 链的选择性官能化。

Pd(ii)-Catalyzed gamma-C(sp)-H alkynylation of amides: selective functionalization of R chains of amides RC(O)NHR.

机构信息

Organic Chemistry Division, CSIR-National Chemical Laboratory (CSIR-NCL), Pune-411008, Maharashtra, India.

出版信息

Chem Commun (Camb). 2018 Jul 11;54(54):7483-7486. doi: 10.1039/c8cc03445a. Epub 2018 Jun 19.

Abstract

The gamma C(sp)-H bond alkynylation of R chains of amides RC(O)NHR, a fundamental class of synthetic substrates, has not been accomplished to date. Here, the first example of palladium(ii)-catalyzed alkynylation of an unactivated gamma C(sp)-H bond of alkyl amides (cyclic, linear, and amino acids) is reported. The kinetic experiment shows that the rate of the reaction depends on the coupling partners and the amides. Late-stage diversification of alkynylated amides was developed by utilizing amine and alkyne functionalities.

摘要

迄今为止,酰胺 RC(O)NHR 的 R 链的γC(sp)-H 键炔基化反应,这一基本的合成底物尚未实现。本文首次报道了钯(ii)催化的未活化的烷基酰胺(环状、直链和氨基酸)的γC(sp)-H 键的炔基化反应。动力学实验表明,反应速率取决于偶联伙伴和酰胺。通过利用胺和炔烃官能团,开发了炔基化酰胺的晚期多样化。

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