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The stereochemistry of the major isomer, C
15H
24O
2, resulting from the epoxidation of
![[gamma]](/logos/entities/gamma_rmgif.gif)
-
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.
Supporting information
![cif](https://journals.iucr.org//../logos/filetypeicons/bw/b1/ciflogo.png) | Crystallographic Information File (CIF) Contains datablock hima |
![hkl](https://journals.iucr.org//../logos/filetypeicons/bw/b1/hkllogo.png) | Structure factor file (CIF format) Supplementary material |
CCDC reference: 128049
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