
%0 Journal Article
%A Eaton, PJ 
%A Hayman, AR 
%A Simpson, J 
%A Weavers, RT 
%T The Chemistry of Laurenene. XI. A Deep-Seated Rearrangement of the Laurenane Skeleton
%J Australian Journal of Chemistry
%D 1990/06/01
%V 43
%N 6
%P 1047-1060
%K 
%R https://doi.org/10.1071/CH9901047
%U https://www.publish.csiro.au/paper/CH9901047 
%X A trifluoroacetic acid induced rearrangement product of laurenan-2&#946;-ol (3) has been shown to have the 4H-pentaleno[6a,1-c]indene skeleton. This combination of one six- membered ring and three five-membered rings has been encountered once previously, again as a rearrangement product of the laurenane skeleton. The structure was determined by n.m.r. studies and by X-ray crystallography conducted primarily on a stable ozonide (6). 
