Journal of Organic Chemistry p. 260 - 267 (1987)
Update date:2022-08-15
Topics:
Fain, Dominique
Dubois, Jacques-Emile
Ion pairing, ring opening, and the rates of formation of aryl-bridged chlorinated intermediates are investigated through reactions of mixed 1,2-dihalo-3-arylpropanes and 1,3-dihalo-2-arylpropanes (aryl = C6H4X with X = H and X = p-Me) and are compared with previous results for X = p-OMe; this allows an estimation of the free energy difference between isomeric aryl-bridged (3-bromopropylene)benzenium ions and bromine-bridged 3-arylpropylenebromonium ions.
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(1987)