75328-57-3Relevant articles and documents
Enhanced Solvolytic Reactivity of 1-Bromobicycloheptane: Intermediacy of a Stabilised Bridgehead Carbenium Ion
Della, Ernest W.,Pigou, Paul E.,Tsanaktsidis, John
, p. 833 - 834 (1987)
1-Bromobicycloheptane displays greater solvolytic reactivity than t-butyl bromide and produces a bridgehead carbenium ion which appears to be stabilised by transannular orbital interactions.
THROUGH-SPACE EFFECTS OF SUBSTITUENTS ON THE STABILITY OF THE 1-BICYCLOHEPTYL CATION.
Della, Ernest W.,Elsey, Gordon M.
, p. 1299 - 1302 (2007/10/02)
γ-Substituents are shown to have a dramatic effect on the stabilisation of the cationic transition state for solvolysis of 5-substituted bicycloheptyl bromides.