
TY  - JOUR
A1  - Kagi, RI 
A1  - Johnson, BL 
T1  - Substituted <I>endo</I>-Tricyclo[3,2,1,0<sup>2,4</sup>]oct-6-enes. II. Selective reductive dechlorination, hydrolysis and other reactions
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1975
VL  - 28
IS  - 10
SP  - 2189
EP  - 2205
KW  - 
UR  - https://doi.org/10.1071/CH9752189 
N2  - 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. 
ER  -

