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...
المؤلفون الرئيسيون: | Willis, M, Claverie, C, Mahon, M |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2002
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مواد مشابهة
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Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
حسب: Willis, M, وآخرون
منشور في: (2002) -
Enantioselective desymmetrisations: The first intermolecular Suzuki couplings producing stereodefined sp3 carbon centres.
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Intramolecular palladium-catalyzed direct arylation of alkenyl triflates.
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Ligand-dependent stereoselective Suzuki–Miyaura cross-coupling reactions of β-enamido triflates
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منشور في: (2021-10-01) -
The selective preparation and Suzuki coupling reactivity of cyclic 1,3-dione derived mono- and ditriflates
حسب: Willis, M, وآخرون
منشور في: (2001)