Substituted endo-Tricyclo[3,2,1,0^2,4]oct-6-enes. II. Selective reductive dechlorination, hydrolysis and other reactions

Abstract

Several reactions of some chloro-, chloromethoxy- and methoxy- substituted endo-tricyclo[3,2,1,0^2,4]-oct-6-enes and endo- tricyclo[3,2,1,0^2,4]octanes have been investigated. These reactions include selective reductive dehalogenation and acetal as well as enol- ether hydrolyses, which, together with other reactions, have furnished some tricyclo[3,2,1,0^2,4]octyl derivatives suitable for magnetic resonance studies.