
TY  - JOUR
A1  - Hayman, AR 
A1  - Perry, NB 
A1  - Weavers, RT 
T1  - The Chemistry of Laurenene. XII. The Structure of a Minor Product From the Formic Acid Induced Rearrangement of Lauren-1-ene
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1990
VL  - 43
IS  - 6
SP  - 1061
EP  - 1069
KW  - 
UR  - https://doi.org/10.1071/CH9901061 
N2  - 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. 
ER  -

