
TY  - JOUR
A1  - Kozyrod, RP 
A1  - Pinhey, JT 
T1  - Arylation with Aryllead Triacetates Produced <i>in situ</i> by Mercury-Lead Exchange
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1985
VL  - 38
IS  - 8
SP  - 1155
EP  - 1161
KW  - 
UR  - https://doi.org/10.1071/CH9851155 
N2  - The addition of lead tetraacetate to diphenylmercury in chloroform leads to the rapid formation of a solution of phenyllead triacetate, which has been used directly for the C-phenylation of ethyl 2-oxocyclopentanecarboxylate (1) and 2-nitropropane in good yield. This method of arylation has been examined for a range of diorganolead compounds and the &#946;-keto ester (1), and the results indicate that the method should be widely applicable. 
ER  -

