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超亲电催化下通过氢/氘交换实现失活芳基卤化物的氘代

Perdeuteration of Deactivated Aryl Halides by H/D Exchange under Superelectrophile Catalysis.

作者信息

He Tao, Klare Hendrik F T, Oestreich Martin

机构信息

Institut für Chemie, Technische Universität Berlin, Strasse des 17. Juni 115, 10623 Berlin, Germany.

出版信息

J Am Chem Soc. 2022 Mar 23;144(11):4734-4738. doi: 10.1021/jacs.2c00080. Epub 2022 Mar 8.

Abstract

Superelectrophilic silylium/arenium ions are shown to be highly effective H/D exchange promoters for the exhaustive deuteration of electron-deficient aryl halides. Several of the resulting perdeuterated aryl halides have been previously inaccessible with existing deuterium-labeling procedures. Using inexpensive CD as the deuterium source, excellent degrees of deuterium incorporation were achieved under ambient reaction conditions. Importantly, the perdeuteration remains unaffected on multigram scale, even at a reduced catalyst loading of 0.1 mol %. By this method, otherwise expensive or noncommercially available NMR solvents such as 1,2-dichloro- and 1,2-difluorobenzene can be prepared.

摘要

超亲电硅鎓/芳鎓离子被证明是用于缺电子芳基卤化物彻底氘代的高效H/D交换促进剂。通过现有的氘标记程序,之前无法获得几种由此产生的全氘代芳基卤化物。使用廉价的CD作为氘源,在环境反应条件下实现了优异的氘掺入程度。重要的是,即使在催化剂负载量降至0.1 mol%的情况下,多克规模的全氘代反应仍不受影响。通过这种方法,可以制备原本昂贵或非商业可得的NMR溶剂,如1,2-二氯苯和1,2-二氟苯。

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