Journal of the Chemical Society. Chemical communications p. 242 - 244 (1986)
Update date:2022-07-29
Topics:
Tanaka, Jiro
Nojima, Masatomo
Kusabayashi, Shigekazu
The reaction of 1-arylpropenyl-lithium (1a-c) with t-alkyl bromides proceeds by either a nucleophilic substitution or single electron transfer mechanism, the preferred pathway being a function of electronic substituent effects and the absence or presence of tetramethylethylenediamine or hexamethylphosphoramide.
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Doi:10.1055/s-2008-1077962
(2008)Doi:10.1016/0039-128X(86)90076-0
(1986)Doi:10.1016/S0040-4020(01)90616-7
(1986)Doi:10.1016/j.molcata.2014.09.040
(2015)Doi:10.1021/jm00387a014
(1987)Doi:10.1021/ic8006475
(2008)
