1986
DOI: 10.1002/mrc.1260240321
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Carbon‐13 NMR spectra of five sesquiterpenes isolated from Ylang Ylang essential oil

Abstract: 13C NMR chemical shifts are given for germacrene‐D, α‐humulene, δ‐cadinene, ε‐cadinene and γ‐muurolene isolated from Ylang Ylang (Cananga odorata, forma genuina) essential oil.

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Cited by 22 publications
(11 citation statements)
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“…This spectrum also showed a signal at δ 0.51 (m), suggesting the presence of a cyclopropane ring in the structure of 10. The observation of a double-multiplete at δ 48.6, in the gated 13 C NMR spectrum with J 163 Hz, characteristic of three member ring, 9 confirms the cyclopropane ring in the molecule. The HMQC spectrum showed long-range correlations between carbons and hydrogens ( Table 1).…”
Section: Resultsmentioning
confidence: 74%
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“…This spectrum also showed a signal at δ 0.51 (m), suggesting the presence of a cyclopropane ring in the structure of 10. The observation of a double-multiplete at δ 48.6, in the gated 13 C NMR spectrum with J 163 Hz, characteristic of three member ring, 9 confirms the cyclopropane ring in the molecule. The HMQC spectrum showed long-range correlations between carbons and hydrogens ( Table 1).…”
Section: Resultsmentioning
confidence: 74%
“…The hexane extract of the leaves of P. macrocarpa was submitted to chromatographic separations to give two sesquiterpenes: spathulenol (7) and macrocarp-11(15)-en-8-ol (10), one diterpene: phytol (11) and two steroids: sistosta-5,25-dien-3β-ol (12) and sitosta-5,22,25-trien-3β-ol (13). The sesquiterpene 7, the diterpene 11 and the steroids 12 and 13 were identified by analysis of their 1 H and 13 C NMR data and comparison with data described in the literature.…”
Section: Resultsmentioning
confidence: 99%
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