Ion-tagged π-acidic alkene ligands promote Pd-catalysed allyl-aryl couplings in an ionic liquid

P.S. Bäuerlein; I.J.S. Fairlamb; A.G. Jarvis; A.F. Lee; C. Müller; J.M. Slattery; R.J. Thatcher; D. Vogt; A.C. Whitwood

doi:10.1039/b906823f

Ion-tagged π-acidic alkene ligands promote Pd-catalysed allyl-aryl couplings in an ionic liquid

P.S. Bäuerlein
, I.J.S. Fairlamb
, A.G. Jarvis
, A.F. Lee
, C. Müller
, J.M. Slattery
, R.J. Thatcher
, D. Vogt
, A.C. Whitwood

Onderzoeksoutput: Bijdrage aan tijdschrift › Tijdschriftartikel › Academic › peer review

19 Citaten (Scopus)

Samenvatting

Ionic p-acidic alkene ligands based on chalcone and benzylidene acetone frameworks have been ?doped? into ionic liquids to provide functional reaction media for Pd-catalysed cross-couplings of a cyclohexenyl carbonate with aryl siloxanes that allow simple product isolation, free from Pd (

Originele taal-2	Engels
Pagina's (van-tot)	5734-5736
Tijdschrift	Chemical Communications, ChemComm
Volume	2009
Nummer van het tijdschrift	38
DOI's	https://doi.org/10.1039/b906823f
Status	Gepubliceerd - 2009

Toegang tot document

10.1039/b906823f

Citeer dit

@article{08cb887fda4343aa9c971c92a7b471c2,

title = "Ion-tagged π-acidic alkene ligands promote Pd-catalysed allyl-aryl couplings in an ionic liquid",

abstract = "Ionic p-acidic alkene ligands based on chalcone and benzylidene acetone frameworks have been ?doped? into ionic liquids to provide functional reaction media for Pd-catalysed cross-couplings of a cyclohexenyl carbonate with aryl siloxanes that allow simple product isolation, free from Pd (",

author = "P.S. B{\"a}uerlein and I.J.S. Fairlamb and A.G. Jarvis and A.F. Lee and C. M{\"u}ller and J.M. Slattery and R.J. Thatcher and D. Vogt and A.C. Whitwood",

year = "2009",

doi = "10.1039/b906823f",

language = "English",

volume = "2009",

pages = "5734--5736",

journal = "Chemical Communications, ChemComm",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "38",

}

TY - JOUR

T1 - Ion-tagged π-acidic alkene ligands promote Pd-catalysed allyl-aryl couplings in an ionic liquid

AU - Bäuerlein, P.S.

AU - Fairlamb, I.J.S.

AU - Jarvis, A.G.

AU - Lee, A.F.

AU - Müller, C.

AU - Slattery, J.M.

AU - Thatcher, R.J.

AU - Vogt, D.

AU - Whitwood, A.C.

PY - 2009

Y1 - 2009

N2 - Ionic p-acidic alkene ligands based on chalcone and benzylidene acetone frameworks have been ?doped? into ionic liquids to provide functional reaction media for Pd-catalysed cross-couplings of a cyclohexenyl carbonate with aryl siloxanes that allow simple product isolation, free from Pd (

AB - Ionic p-acidic alkene ligands based on chalcone and benzylidene acetone frameworks have been ?doped? into ionic liquids to provide functional reaction media for Pd-catalysed cross-couplings of a cyclohexenyl carbonate with aryl siloxanes that allow simple product isolation, free from Pd (

U2 - 10.1039/b906823f

DO - 10.1039/b906823f

M3 - Article

C2 - 19774252

SN - 1359-7345

VL - 2009

SP - 5734

EP - 5736

JO - Chemical Communications, ChemComm

JF - Chemical Communications, ChemComm

IS - 38

ER -

Ion-tagged π-acidic alkene ligands promote Pd-catalysed allyl-aryl couplings in an ionic liquid

Samenvatting

Toegang tot document

Vingerafdruk

Citeer dit