Dual Ligand Enabled Pd-Catalyzed Ortho-Alkylation of Iodoarenes DOI Creative Commons
X.J. Wang, Lei Jiao

Published: May 10, 2024

The synthesis of complex polysubstituted aromatic molecules from simple precursors is a central goal in organic chemistry. In this study, we developed an approach for the ortho-alkylation iodoarenes utilizing dual ligand catalytic system. By combining Pd/olefin cooperative catalysis with bulky trialkylphosphine ligand-promoted C(sp2)-I reductive elimination, have established ortho-alkylative Catellani-type reaction aryl-iodine bond reconstruction as final step, which opens new synthetic opportunities within reactions. Through in-depth mechanistic investigations, isolated and characterized key organopalladium intermediates, revealing synergistic interaction ligands merging process elimination. present study showcases unique advantages emphasizes effectiveness system expanding chemical space Catellani

Language: Английский

Dual Ligand Enabled Pd-Catalyzed Ortho-Alkylation of Iodoarenes DOI Creative Commons
X.J. Wang, Lei Jiao

Published: May 10, 2024

The synthesis of complex polysubstituted aromatic molecules from simple precursors is a central goal in organic chemistry. In this study, we developed an approach for the ortho-alkylation iodoarenes utilizing dual ligand catalytic system. By combining Pd/olefin cooperative catalysis with bulky trialkylphosphine ligand-promoted C(sp2)-I reductive elimination, have established ortho-alkylative Catellani-type reaction aryl-iodine bond reconstruction as final step, which opens new synthetic opportunities within reactions. Through in-depth mechanistic investigations, isolated and characterized key organopalladium intermediates, revealing synergistic interaction ligands merging process elimination. present study showcases unique advantages emphasizes effectiveness system expanding chemical space Catellani

Language: Английский

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