Abstract
A detailed account of the
synthesis of three related bicyclo[2,2,2]octenyl carbinols (3),(4) and (5) and
their behaviour in acidified methanol is presented. Seventeen different
compounds which are intermediates of final stable end products have been isolated
and characterized. In each case the products of acid-catalysed isomerization
can be explained by postulating rearrangements involving stabilized carbonium
ions.
Cited by
7 articles.
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