Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling

M C Willis; C K Claverie; M F Mahon

doi:10.1039/b200692h

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling

M C Willis, C K Claverie, M F Mahon

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

13 Citations (SciVal)

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 language	English
Pages (from-to)	832-833
Number of pages	2
Journal	Chemical Communications
Issue number	8
DOIs	https://doi.org/10.1039/b200692h
Publication status	Published - 2002

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ID number: ISI:000174999900016

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10.1039/b200692h

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@article{b0bf3d4e783c48a2a579c5f8bd4bff18,

title = "Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling",

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.",

author = "Willis, \{M C\} and Claverie, \{C K\} and Mahon, \{M F\}",

note = "ID number: ISI:000174999900016",

year = "2002",

doi = "10.1039/b200692h",

language = "English",

pages = "832--833",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "8",

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T1 - Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling

AU - Willis, M C

AU - Claverie, C K

AU - Mahon, M F

N1 - ID number: ISI:000174999900016

PY - 2002

Y1 - 2002

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/0037149961

U2 - 10.1039/b200692h

DO - 10.1039/b200692h

M3 - Article

SN - 1359-7345

SP - 832

EP - 833

JO - Chemical Communications

JF - Chemical Communications

IS - 8

ER -

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling

Abstract

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