4.8 Article

Regio- and Stereoselective Synthesis of Functionalized Dihydropyridines, Pyridines, and 2H-Pyrans: Heck Coupling of Monocyclopropanated Heterocycles

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 11, Pages 3594-3598

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201813716

Keywords

2H-pyrans; arylpyridines; dihydropyridines; donor-acceptor cyclopropanes; Heck coupling

Funding

  1. DAAD
  2. DFG [GRK 1910]

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A palladium-catalyzed coupling between aryl halides and monocyclopropanated pyrroles or furans has been developed, leading to valuable six-membered N- and O-heterocycles. As the key step, a selective cleavage of the non-activated endocyclic C-C bond of the 2-heterobicyclo-[3.1.0]hexane framework is achieved. The developed method offers access to highly functionalized piperidines, pyridines, and pyrans that are challenging to access by traditional methods.

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