
%0 Journal Article
%A Hanton, LR 
%A Simpson, J 
%A Weavers, RT 
%T The chemistry of lauren-1-ene. V. The structure of an acid-catalysed rearrangement product
%J Australian Journal of Chemistry
%D 1983/12/01
%V 36
%N 12
%P 2581-2586
%K 
%R https://doi.org/10.1071/CH9832581
%U https://www.publish.csiro.au/paper/CH9832581 
%X The major product from the formic-acid-induced rearrangement of lauren-1-ene has been confirmed to be (1S,4S,8R,9S,12R)-4,8,12,14,15-pentamethyltetracyclo[10,3,0,01,9,O4,9]pentadec-14-ene by X-ray analysis of a derived diol. 
