Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202301556
Keywords
Allylic C-H Functionalization; 1; 4-Hydrofunctionalization; 4; 3-Hydrofunctionalization; Regiodivergent; Remote Substitution
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This study describes feasible protocols to achieve regiodivergent allylic C-H functionalizations via palladium-catalyzed remote substitution, which provides a novel strategy for the seldomly studied migratory Tsuji-Trost reaction. Dictated by a suitable ligand, a process involving 4,3-hydrofunctionalization of the generated conjugated diene intermediate via metal walking is observed with generally >20 : 1 regioselectivity. A major route is also found for 1,4-hydrofunctionalization with a newly synthesized electron-rich bisphosphine ligand.
Different from classical allylic substitutions that require a vicinal leaving group, an olefin bearing a remote leaving group is scarcely viewed as a potential allylation substrate. Herein, we describe feasible protocols to achieve regiodivergent allylic C-H functionalizations via palladium-catalyzed remote substitution, which provides a novel strategy for the seldomly studied migratory Tsuji-Trost reaction. Dictated by a suitable ligand, a process that involved 4,3-hydrofunctionalization of the generated conjugated diene intermediate via metal walking is observed in generally >20 : 1 regioselectivity. Unexpectedly, a related 1,4-hydrofunctionalization pathway is found to be a major route with a newly synthesized electron-rich bisphosphine ligand, which challenges the conventional viewpoint on the potential regioselectivity of hydrofunctionalizations of linear internal conjugated dienes via eta(3)-substitution. A series of deuterium experiments and kinetic studies provide a preliminary insight into the potential catalytic cycle.
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