Transition metal-catalysed directed C–H functionalization with nucleophiles

亲核细胞 化学 杂原子 组合化学 试剂 有机合成 偶联反应 金属有机化学 过渡金属 催化作用 有机化学 戒指(化学)
作者
Sergio Barranco,Jiayu Zhang,Sara López,Alessandra Casnati,Mónica H. Pérez‐Temprano
出处
期刊:Nature Synthesis [Springer Nature]
卷期号:1 (11): 841-853 被引量:24
标识
DOI:10.1038/s44160-022-00180-8
摘要

The quest for sustainable ways to introduce diverse functional groups onto complex scaffolds has made directed transition metal-catalysed C–H functionalization reactions a main thrust within synthetic organic chemistry. These methodologies offer appealing opportunities to construct carbon–carbon and carbon–heteroatom bonds by using a wide array of coupling partners. Strikingly, organometallic and X-based (X = N, O and S) nucleophiles, which are key reagents in cross-coupling reactions, remain underexploited in these transformations. However, as a result of fine-tuning the reaction conditions and a better understanding of the underlying mechanisms, these reagents were recently incorporated into the synthetic toolkit of C–H functionalizations. This Review outlines a selection of recent advances in nucleophilic C–C and C–heteroatom bond-forming reactions via directed C–H activation. We focus on catalytic approaches that involve organometallic nucleophiles and X-based (X = N, O and S) coupling partners and describe how the field has evolved towards innovative strategies that enhance the applicability and versatility of these transformations. In addition, we highlight synthetic challenges that remain unsolved and that could open exciting venues within this area.
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