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Published in 2021 at "Synlett"
DOI: 10.1055/a-1523-3228
Abstract: We report a ligand-controlled nickel-catalyzed reductive hydroarylation of styrenes with predictable and controllable regioselectivity. With a diamine ligand, the reaction produces selective linear hydroarylation products. Alternatively, with a chiral PyrOx ligand, branch-selective enantioenriched 1,1-diarylalkane products…
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Keywords:
nickel catalyzed;
hydroarylation styrenes;
catalyzed regiodivergent;
reductive hydroarylation ... See more keywords