Abstract
Turpentine from cortical oleoresin of Abies magnifica A. Murr. was analyzed by a combination of gas-liquid and column chromatography, and the individual materials separated were identified by u.v., i.r., Raman, nuclear magnetic resonance (NMR), and mass spectral (MS) data as well as by the GLC retention data. Nineteen monoterpenoids and twenty-six sesquiterpene hydrocarbons were identified (Tables 1 and 2) including two new compounds, γ-humulene and cyclosativene, whose structures were determined.
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