Seeking selectivity in alkene couplings

IF 42.8 1区化学 Q1 CHEMISTRY, PHYSICAL

Nature Catalysis Pub Date : 2024-11-21 DOI:10.1038/s41929-024-01242-0

Patricia Brizuela, M. Teresa Quirós

引用次数: 0

Abstract

Metal-catalysed multicomponent cross-coupling reactions enable the efficient and diverse synthesis of complex molecules. Now, clever use of anionic ligands facilitates the coordination of native functional groups to the catalyst to control regioselectivity, avoiding the installation of directing groups and expanding the accessible chemical space.

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寻求烯烃耦合的选择性

金属催化的多组分交叉偶联反应可以高效、多样地合成复杂分子。现在，阴离子配体的巧妙使用有助于将原生官能团配位到催化剂上，从而控制区域选择性，避免了定向基团的安装，扩大了可利用的化学空间。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Nature Catalysis Chemical Engineering-Bioengineering

CiteScore

52.10

自引率

1.10%

发文量

140

期刊介绍： Nature Catalysis serves as a platform for researchers across chemistry and related fields, focusing on homogeneous catalysis, heterogeneous catalysis, and biocatalysts, encompassing both fundamental and applied studies. With a particular emphasis on advancing sustainable industries and processes, the journal provides comprehensive coverage of catalysis research, appealing to scientists, engineers, and researchers in academia and industry. Maintaining the high standards of the Nature brand, Nature Catalysis boasts a dedicated team of professional editors, rigorous peer-review processes, and swift publication times, ensuring editorial independence and quality. The journal publishes work spanning heterogeneous catalysis, homogeneous catalysis, and biocatalysis, covering areas such as catalytic synthesis, mechanisms, characterization, computational studies, nanoparticle catalysis, electrocatalysis, photocatalysis, environmental catalysis, asymmetric catalysis, and various forms of organocatalysis.