2024-03-29T15:46:34Zhttps://uvadoc.uva.es/oai/requestoai:uvadoc.uva.es:10324/217282021-06-24T07:42:13Zcom_10324_1186com_10324_931com_10324_894com_10324_28542com_10324_952col_10324_1404col_10324_28543
Carrasco Fernández, Desiré
Pérez Temprano, Mónica H.
Casares González, Juan Ángel
Espinet Rubio, Pablo
2016-12-14T13:37:27Z
2016-12-14T13:37:27Z
2014
Organometallics, 2014, 33 (13), p. 3540–3545
0276-7333
http://uvadoc.uva.es/handle/10324/21728
10.1021/om500446x
13
American Chemical Society
33
Experiments on palladium catalyzed cross-coupling of [AuMe(PPh3)] with aryl iodides show that Ar–Ar homocoupling products are the main product or an abundant byproduct of the reaction. The percentage of cross-coupling product is higher for aryls with larger p Hammet parameter. The scrambling of organic groups via bimetallic intermediates explains the formation of these products. This scrambling can be observed and the activation energies partially quantified in some cases using as aryl C6Cl2F3, which is relatively reluctant to coupling.
eng
info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-nd/4.0/
Attribution-NonCommercial-NoDerivatives 4.0 International
Catalyst
Cross Alkyl-Aryl Versus Homo Aryl-Aryl Coupling in Pdcatalyzed Coupling of Alkyl-Gold(I) and Aryl-X (X = Halide)
info:eu-repo/semantics/article