Buy article online - an online subscription or single-article purchase is required to access this article.
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.
-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.
journal menu







,3
,8
Subscribe to Acta Crystallographica Section C: Structural Chemistry


