Nickel-Catalyzed Aryl Borylations: Opportunities and Challenges for Innovation

化学 芳基 硼酸化 一套 功能(生物学) 生化工程 组合化学 反应性(心理学) 纳米技术 国家(计算机科学) 风险分析(工程) 合理设计 配体(生物化学) 硼酸 还原消去 光学(聚焦) 管理科学 可持续发展
作者
Joshua B. McManus,Grace P. Ahlqvist,Colton R. Davis,Louis de Lescure,Vaishnavi N. Nair,Andreas R. Rötheli,Brenda J. Burke,Jason S. Tedrow
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:148 (1): 1-19 被引量:1
标识
DOI:10.1021/jacs.5c16385
摘要

The utility of aryl boronic acids, esters, and their congeners has led to the development of methods spanning from early synthesis strategies via deprotonations and metal/halogen exchange protocols to sophisticated and well-studied Pd-catalyzed Miyaura borylations and Ir-catalyzed C-H activations. Ni catalysis has also emerged as an approach that is not only more economical and environmentally sustainable than precious metal catalysis but also enables access to mechanistic pathways and substrates that are typically inaccessible with Pd catalysis. While Ni-catalyzed aryl borylations have been successfully demonstrated in the academic and industrial literature for decades, the lack of general conditions and Ni-specific reaction design studies prevents broader application of these methods. In this Perspective, we discuss the current state of the literature regarding Ni-catalyzed aryl borylation and suggest areas of focus for continued study. Advances in mechanistic insight, rational ligand design, high-throughput platforms, and machine-learning models will be instrumental in establishing dependable starting conditions that may largely eliminate the need for cumbersome substrate-tailored optimization. Ni-catalyzed aryl borylations have shown enough promise to become a prominent topic in the current literature, and developing a well-understood suite of general reaction conditions will allow this mode of reactivity to become a competitive borylative strategy.
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