
TY  - JOUR
A1  - Della, EW 
A1  - Taylor, DK 
T1  - Synthesis and Solvolysis of 1-Bromobicyclo[1.1.1]pentane
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1990
VL  - 43
IS  - 5
SP  - 945
EP  - 948
KW  - 
UR  - https://doi.org/10.1071/CH9900945 
N2  - 1-Bromobicyclo[1.1.1]pentane (3) is found to undergo solvolysis faster than t-butyl bromide in 80% aqueous ethanol, and gives 3-methylenecyclobutanol (7) exclusively. Products arising from capture of the bicyclo[1.1.1] pentyl cation (5) were not detected. 
ER  -

