1.
Chem Commun (Camb)
; (23): 2752-3, 2004 Dec 07.
Article
in English
| MEDLINE
| ID: mdl-15568100
ABSTRACT
A triphenylphosphine having a strong electron-donating group, an oxyanion, at the para position of one of the benzene rings was found to show much higher efficiency compared with other structurally related triarylphosphines in the palladium-catalysed arylation of alkenes.
