
The stereochemistry of the major isomer, C15H24O2, resulting from the epoxidation of
-trans-himachalene has been established and hence, the configurations of the resulting derivatives have been deduced. The seven-membered ring is chair shaped while the six-membered ring adopts a 1,2-diplanar conformation.
![[gamma]](/logos/entities/gamma_rmgif.gif)
Supporting information
![]() | Crystallographic Information File (CIF) |
![]() | Structure factor file (CIF format) |
CCDC reference: 128049