Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling

M C Willis, C K Claverie, M F Mahon

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

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 tricycliccarbocycles.
Original languageEnglish
Pages (from-to)832-833
Number of pages2
JournalChemical Communications
Issue number8
DOIs
Publication statusPublished - 2002

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Boronic Acids
Cyclization
Palladium
Cesium
Acetates
Acids
cesium fluoride
vinyl triflate
triphenylphosphine

Cite this

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling. / Willis, M C; Claverie, C K; Mahon, M F.

In: Chemical Communications, No. 8, 2002, p. 832-833.

Research output: Contribution to journalArticle

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