2022-10-27
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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27 p.
Springer-Nature
CERCA Programme/Generalitat de Catalunya
Ministerio de Ciencia e Innovación/Agencia Estatal de Investigación (MICINN/AEI/Severo Ochoa Excellence Accreditation 2023 – CEX2019-000925-S; grant no. PID2020-112733GB-I00)
S.B. thanks the Ministerio de Universidades for the FPU pre-doctoral contract (FPU20/00610).
J.Z. thanks the China Scholarship Council for the predoctoral fellowship
S.L-R. thanks the Generalitat de Catalunya for the FI–Agaur predoctoral contract.
A.C. the MSCA-COFUND postdoctoral fellowship granted by I2-ICIQ Impulsion Programme (GA 801474).
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