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• W2598530107 abstract "Meta-C−H functionalization of benzylamines has been developed using a PdII/transient mediator strategy. Using 2-pyridone ligands and 2-carbomethoxynorbornene (NBE-CO2Me) as the mediator, arylation, amination, and chlorination of benzylamines are realized. This protocol features a broad substrate scope and is compatible with heterocylic coupling partners. Moreover, the loading of the Pd can be lowered to 2.5 mol % by using the optimal ligand." @default.
• W2598530107 created "2017-04-07" @default.
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• W2598530107 date "2017-03-30" @default.
• W2598530107 modified "2023-10-16" @default.
• W2598530107 title "Ligand-Promoted<i>meta</i>-C−H Functionalization of Benzylamines" @default.
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• W2598530107 doi "https://doi.org/10.1002/anie.201701803" @default.
• W2598530107 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5512280" @default.
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