[Pd(IPr*)(cinnamyl)Cl]: an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

Anthony Raymond Georges Chartoire; Mathieu Lesieur; Laura Falivene; Alexandra Martha Zoya Slawin; Luigi Cavallo; Catherine S.J. Cazin; Steven Patrick Nolan

doi:10.1002/chem.201104009

[Pd(IPr*)(cinnamyl)Cl]: an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

Anthony Raymond Georges Chartoire, Mathieu Lesieur, Laura Falivene, Alexandra Martha Zoya Slawin, Luigi Cavallo, Catherine S.J. Cazin^*, Steven Patrick Nolan^*

^*Corresponding author for this work

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

Original language	English
Pages (from-to)	4517-4521
Number of pages	5
Journal	Chemistry - A European Journal
Volume	18
Issue number	15
Early online date	13 Mar 2012
DOIs	https://doi.org/10.1002/chem.201104009
Publication status	Published - 10 Apr 2012

Keywords

Biaryls
Cross-coupling
N-heterocyclic carbenes
Palladium

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10.1002/chem.201104009

Cite this

@article{ef623b91c64e43e4b1dfeccf095d017a,

title = "[Pd(IPr*)(cinnamyl)Cl]: an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling",

keywords = "Biaryls, Cross-coupling, N-heterocyclic carbenes, Palladium",

author = "Chartoire, \{Anthony Raymond Georges\} and Mathieu Lesieur and Laura Falivene and Slawin, \{Alexandra Martha Zoya\} and Luigi Cavallo and Cazin, \{Catherine S.J.\} and Nolan, \{Steven Patrick\}",

note = "Funding: The authors gratefully acknowledge the EC for funding through the seventh framework programme SYNFLOW. We thank the EPSCR National Mass Spectrometry Service Center in Swansea for mass spectrometric analyses. Umicore AG is thanked for its generous gifts of materials. S.P.N. is a Royal Society Wolfson Research Merit Award holder. C.S.J.C. acknowledges the Royal Society for a University Research Fellowship.",

year = "2012",

month = apr,

day = "10",

doi = "10.1002/chem.201104009",

language = "English",

volume = "18",

pages = "4517--4521",

journal = "Chemistry - A European Journal",

issn = "0947-6539",

publisher = "John Wiley \& Sons, Ltd",

number = "15",

}

TY - JOUR

T1 - [Pd(IPr*)(cinnamyl)Cl]

T2 - an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

AU - Chartoire, Anthony Raymond Georges

AU - Lesieur, Mathieu

AU - Falivene, Laura

AU - Slawin, Alexandra Martha Zoya

AU - Cavallo, Luigi

AU - Cazin, Catherine S.J.

AU - Nolan, Steven Patrick

N1 - Funding: The authors gratefully acknowledge the EC for funding through the seventh framework programme SYNFLOW. We thank the EPSCR National Mass Spectrometry Service Center in Swansea for mass spectrometric analyses. Umicore AG is thanked for its generous gifts of materials. S.P.N. is a Royal Society Wolfson Research Merit Award holder. C.S.J.C. acknowledges the Royal Society for a University Research Fellowship.

PY - 2012/4/10

Y1 - 2012/4/10

KW - Biaryls

KW - Cross-coupling

KW - N-heterocyclic carbenes

KW - Palladium

UR - https://www.scopus.com/pages/publications/84859237473

U2 - 10.1002/chem.201104009

DO - 10.1002/chem.201104009

M3 - Article

SN - 0947-6539

VL - 18

SP - 4517

EP - 4521

JO - Chemistry - A European Journal

JF - Chemistry - A European Journal

IS - 15

ER -

[Pd(IPr*)(cinnamyl)Cl]: an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

Keywords

Access to Document

Other files and links

Studies of homogeneous catalysts: Mechanistic studies of homogeneous catalysts

SYNFLOW 100%: SYNFLOW - 100% Contribution

Wolfson Research Merit Award: Wolfson Research Merit Award

Cite this

[Pd(IPr*)(cinnamyl)Cl]: an efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

Keywords

Access to Document

Other files and links

Projects

Studies of homogeneous catalysts: Mechanistic studies of homogeneous catalysts

SYNFLOW 100%: SYNFLOW - 100% Contribution

Wolfson Research Merit Award: Wolfson Research Merit Award

Cite this