4.6 Article

Palladium-Catalyzed C-H Functionalization of Phenyl 2-Pyridylsulfonates

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 12, Issue 1, Pages 130-144

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201601413

Keywords

acetoxylation; C-H activation; olefination; phenols; regioselectivity

Funding

  1. National Natural Science Foundation of China [NSFC-21272185, 21572178]

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An efficient palladium(II)-catalyzed intermolecular direct ortho-alkenylation and acetoxylation of phenols has been developed. The reaction proceeded via a seven-membered cyclopalladated intermediate and showed complete regio- and diastereoselectivity. The approach also provided an efficient route for the synthesis of coumarins and benzofurans.

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