Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
Treatment of a benzyl substituted meso-ditriflate with boronic acids in the presence of palladium acetate, triphenylphosphine and caesium fluoride results in intermolecular Suzuki coupling followed by vinyl triflate-arene cyclisation to provide, in high yields, single regioisomers of tricyclic-carbo...
Main Authors: | Willis, M, Claverie, C, Mahon, M |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2002
|
Similar Items
-
Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling
by: Willis, M, et al.
Published: (2002) -
The selective preparation and Suzuki coupling reactivity of cyclic 1,3-dione derived mono- and ditriflates
by: Willis, M, et al.
Published: (2001) -
Enantioselective desymmetrisations: The first intermolecular Suzuki couplings producing stereodefined sp3 carbon centres.
by: Powell, L, et al.
Published: (2004) -
Gold-catalyzed intramolecular oxidative cross-coupling of nonactivated arenes.
by: Hopkinson, M, et al.
Published: (2010) -
Intramolecular palladium-catalyzed direct arylation of alkenyl triflates.
by: Cruz, A, et al.
Published: (2007)