
%0 Journal Article
%A Hayman, AR 
%A Perry, NB 
%A Weavers, RT 
%T The Chemistry of Laurenene. XII. The Structure of a Minor Product From the Formic Acid Induced Rearrangement of Lauren-1-ene
%J Australian Journal of Chemistry
%D 1990/06/01
%V 43
%N 6
%P 1061-1069
%K 
%R https://doi.org/10.1071/CH9901061
%U https://www.publish.csiro.au/paper/CH9901061 
%X Rearrangement of lauren-1-ene (1) with formic acid gives a trisubstituted alkene (4) in addition to the previously characterized tetrasubstituted  alkene (3). The structure was determined by n.m.r . Studies on (4) and the derived diol (5). Alkene (4) contains a new tetracyclic carbon skeleton which comprises one six- membered ring and three five- membered rings. 
