dc.contributor.author |
Zeevaart, JG
|
en_US |
dc.contributor.author |
Parkinson, CJ
|
en_US |
dc.contributor.author |
De Koning, CB
|
en_US |
dc.date.accessioned |
2007-02-06T09:17:11Z |
en_US |
dc.date.accessioned |
2007-06-07T10:05:01Z |
|
dc.date.available |
2007-02-06T09:17:11Z |
en_US |
dc.date.available |
2007-06-07T10:05:01Z |
|
dc.date.copyright |
|
en_US |
dc.date.issued |
2004-05-24 |
en_US |
dc.identifier.citation |
Zeevaart, JG, Parkinson, CJ and De Koning, CB. 2004. Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters. Tetrahedron Letters, vol. 45(22), pp 4261-4264 |
en_US |
dc.identifier.issn |
0040-4039 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/10204/1502
|
en_US |
dc.identifier.uri |
http://hdl.handle.net/10204/1502
|
|
dc.description.abstract |
The coupling reaction between ethyl acetoacetate and a number of aryl halides in the presence of palladium acetate, a bulky and electron rich phosphine and K3PO4 is described. The arylated acetoacetate ester is de-acylated under the reaction conditions resulting in the generation of 2-arylacetic acid esters, constituting a mild alternative to direct arylation of carboxylate esters. |
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dc.format.extent |
256012 bytes |
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dc.format.mimetype |
application/pdf |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Pergamon-Elsevier Science Ltd |
en_US |
dc.rights |
Copyright: 2004 Pergamon-Elsevier Science Ltd |
en_US |
dc.source |
|
en_US |
dc.subject |
Palladium catalysis |
en_US |
dc.subject |
Enolate arylation |
en_US |
dc.subject |
Arylacetic acid esters |
en_US |
dc.subject |
Organic chemistry |
en_US |
dc.title |
Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters |
en_US |
dc.type |
Article |
en_US |
dc.identifier.apacitation |
Zeevaart, J., Parkinson, C., & De Koning, C. (2004). Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters. http://hdl.handle.net/10204/1502 |
en_ZA |
dc.identifier.chicagocitation |
Zeevaart, JG, CJ Parkinson, and CB De Koning "Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters." (2004) http://hdl.handle.net/10204/1502 |
en_ZA |
dc.identifier.vancouvercitation |
Zeevaart J, Parkinson C, De Koning C. Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters. 2004; http://hdl.handle.net/10204/1502. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Zeevaart, JG
AU - Parkinson, CJ
AU - De Koning, CB
AB - The coupling reaction between ethyl acetoacetate and a number of aryl halides in the presence of palladium acetate, a bulky and electron rich phosphine and K3PO4 is described. The arylated acetoacetate ester is de-acylated under the reaction conditions resulting in the generation of 2-arylacetic acid esters, constituting a mild alternative to direct arylation of carboxylate esters.
DA - 2004-05-24
DB - ResearchSpace
DP - CSIR
KW - Palladium catalysis
KW - Enolate arylation
KW - Arylacetic acid esters
KW - Organic chemistry
LK - https://researchspace.csir.co.za
PY - 2004
SM - 0040-4039
T1 - Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters
TI - Palladium-catalysed arylation of acetoacetate esters to yield 2-arylacetic acid esters
UR - http://hdl.handle.net/10204/1502
ER -
|
en_ZA |