
%0 Journal Article
%A Kagi, RI 
%A Johnson, BL 
%T Substituted <I>endo</I>-Tricyclo[3,2,1,0<sup>2,4</sup>]oct-6-enes. II. Selective reductive dechlorination, hydrolysis and other reactions
%J Australian Journal of Chemistry
%D 1975/10/01
%V 28
%N 10
%P 2189-2205
%K 
%R https://doi.org/10.1071/CH9752189
%U https://www.publish.csiro.au/paper/CH9752189 
%X Several reactions of some chloro-, chloromethoxy- and methoxy- substituted endo-tricyclo[3,2,1,02,4]-oct-6-enes and endo- tricyclo[3,2,1,02,4]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[3,2,1,02,4]octyl derivatives suitable for magnetic resonance studies. 
