Journal of the Chemical Society. Perkin transactions I p. 1673 - 1676 (1993)
Update date:2022-08-04
Topics:
Morgan, Jacqueline
Pinhey, John T.
o-(Prop-2-enyloxy)phenyllead triacetate 6, which was obtained by treatment of the corresponding boronic acid with lead tetraacetate, has been shown to react with iodide and azide ions, 2,4,6-trimethylphenol, ethyl 2-oxocyclopentanecarboxylate, and the sodium salt of 2-nitropropane to give only those products which, in a formal sense, are derived by direct nucleophilic displacement of the Pb(OAc)3 group.The complete absence of 3-substituted dihydrobenzofurans among the products is strong evidence that aryl free radicals are not involved in the arylation reactions of aryllead triacetates.
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Doi:10.1002/ejoc.201800504
(2018)Doi:10.1385/BTER:77:2:97
()Doi:10.1016/S0957-4166(00)80334-1
(1993)Doi:10.1021/je60021a039
(1964)Doi:10.2165/00019053-200119030-00004
()Doi:10.1016/S0040-4039(00)79166-0
(1993)
