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通过砜的配体偶联反应实现的氮杂芳基氟烷基化

N-Heteroaromatic Fluoroalkylation through Ligand Coupling Reaction of Sulfones.

作者信息

Liang Huamin, Wang Qian, Zhou Xin, Zhang Rongyi, Zhou Min, Wei Jun, Ni Chuanfa, Hu Jinbo

机构信息

Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.

School of Physical Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai, 201210, China.

出版信息

Angew Chem Int Ed Engl. 2024 May 6;63(19):e202401091. doi: 10.1002/anie.202401091. Epub 2024 Apr 8.

Abstract

Ligand coupling on hypervalent main group elements has emerged as a pivotal methodology for the synthesis of functionalized N-heteroaromatic compounds in recent years due to the avoidance of transition metals and the mildness of the reaction conditions. In this direction, the reaction of N-heteroaryl sulfur(IV) and N-heteroaryl phosphorus(V) compounds has been well studied. However, the ligand coupling of sulfur(VI) is still underdeveloped and the reaction of alkyl N-heteroarylsulfones is still elusive, which does not match the high status of sulfones as the chemical chameleons in organic synthesis. Here we present a ligand coupling-enabled formal SO extrusion of fluoroalkyl 2-azaheteroarylsulfones under the promotion of Grignard reagents, which not only enriches the chemistry of sulfones, but also provides a novel and practical synthetic tool towards N-heteroaromatic fluoroalkylation.

摘要

近年来,由于避免使用过渡金属且反应条件温和,高价主族元素上的配体偶联已成为合成功能化氮杂芳族化合物的关键方法。在这个方向上,氮杂芳基硫(IV)和氮杂芳基磷(V)化合物的反应已得到充分研究。然而,硫(VI)的配体偶联仍未得到充分发展,烷基氮杂芳基砜的反应仍然难以捉摸,这与砜在有机合成中作为化学变色龙的崇高地位不相匹配。在此,我们报道了在格氏试剂促进下,氟烷基2-氮杂芳基砜实现了配体偶联驱动的形式上的SO消除反应,这不仅丰富了砜的化学性质,还为氮杂芳族氟烷基化提供了一种新颖且实用的合成工具。

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