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调控金属物种作为 Ni 催化炔烃与水的立体发散半氢化反应的控制点。

Modulation of metal species as control point for Ni-catalyzed stereodivergent semihydrogenation of alkynes with water.

机构信息

Jilin Provincial Key Laboratory of Carbon Fiber Development and Application, College of Chemistry and Life Science, Advanced Institute of Materials Science, Changchun University of Technology, 130012, Changchun, PR China.

Department of Chemistry, Fudan University, 200438, Shanghai, PR China.

出版信息

Nat Commun. 2023 Mar 24;14(1):1655. doi: 10.1038/s41467-023-37022-w.

Abstract

A base-assisted metal species modulation mechanism enables Ni-catalyzed stereodivergent transfer semihydrogenation of alkynes with water, delivering both olefinic isomers smoothly using cheap and nontoxic catalysts and additives. Different from most precedents, in which E-alkenes derive from the isomerization of Z-alkene products, the isomers were formed in orthogonal catalytic pathways. Mechanistic studies suggest base as a key early element in modulation of the reaction pathways: by adding different bases, nickel species with disparate valence states could be accessed to initiate two catalytic cycles toward different stereoisomers. The practicability of the method is showcased with nearly 70 examples, including internal and terminal triple bonds, enynes and diynes, affording semi-hydrogenated products in high yields and selectivity.

摘要

一种基于助剂的金属物种调制机制使镍催化的炔烃与水的立体发散转移半氢化反应成为可能,使用廉价且无毒的催化剂和添加剂顺利地得到了两种烯烃异构体。与大多数先例不同,其中 E-烯烃是由 Z-烯烃产物的异构化产生的,而这些异构体则是在正交催化途径中形成的。机理研究表明,碱是调节反应途径的关键早期因素:通过添加不同的碱,可以获得具有不同价态的镍物种,从而引发两个催化循环,生成不同的立体异构体。该方法的实用性在近 70 个实例中得到了展示,包括内部和末端三键、烯炔和二炔,以高产率和选择性得到半氢化产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c8/10039052/a057091fedda/41467_2023_37022_Fig1_HTML.jpg

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