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...
Hauptverfasser: | Willis, M, Claverie, C, Mahon, M |
---|---|
Format: | Journal article |
Sprache: | English |
Veröffentlicht: |
2002
|
Ähnliche Einträge
Ähnliche Einträge
-
Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
von: Willis, M, et al.
Veröffentlicht: (2002) -
Enantioselective desymmetrisations: The first intermolecular Suzuki couplings producing stereodefined sp3 carbon centres.
von: Powell, L, et al.
Veröffentlicht: (2004) -
Intramolecular palladium-catalyzed direct arylation of alkenyl triflates.
von: Cruz, A, et al.
Veröffentlicht: (2007) -
Ligand-dependent stereoselective Suzuki–Miyaura cross-coupling reactions of β-enamido triflates
von: Tomáš Chvojka, et al.
Veröffentlicht: (2021-10-01) -
The selective preparation and Suzuki coupling reactivity of cyclic 1,3-dione derived mono- and ditriflates
von: Willis, M, et al.
Veröffentlicht: (2001)