Journal of the Chemical Society. Chemical communications p. 1513 - 1514 (1986)
Update date:2022-08-16
Topics:
Davies, Alwyn G.
Hay-Montherwell, Robyn S.
Evans, Jeffrey C.
Rowlands, Christopher C.
1,4-Dimethylcyclohexa-1,3-diene reacts with (4-BrC6H4)3N(.+)SbCl6(-) by a mechanism involving both proton and electron hole catalysis to give the product of the cyclo-addition between the parent diene and 2,5-dimethylcyclohexa-1,3-diene acting as the dienophile; the persistent e.s.r. spectrum of the adduct can be observed.
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