Author:
Gream GE,Serelis AK,Stoneman TI
Abstract
Acetolysis of
4-(cyclopent-1'-enyl)butyl and 3-(2'-methylenecyclopentyl)propyl derivatives,
but not 3-(cyclohex-1'-enyl)propyl and 2-(2'-methylenecyclohexyl)ethyl
derivatives, occurs with π-bond participation (95 and 92%, respectively)
to give similar, including maybe identical, cationic species involving the
8-hydrindyl cation. On the basis of product composition, the 8-hydrindyl
cations when generated from spiro[4,4]non-1-yl (σ-route) and cis- and trans-8-hydrindyl derivatives (direct route) are each different and
are in turn different to those generated by the above π-routes. Reasons
for the differences are discussed and the possible role of the counter-ion in
ion-pairs is examined.
Cited by
17 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献