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Δ2-Triterpenes: Early intermediates in the diagenesis of terrigenous triterpenoids
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“Δ2-boswellic and Δ2-lupeolic acids constitute another group of diagnostic compounds, which are identified here for the first time. They were not detected when analyzing the modern reference resins and may be considered as first stage degradation products of boswellic and lupeolic acids, i.e. they are most likely formed by dehydration of the 3α alcohol functionality (Figure 8) as is the case for am”
From Holy Smoke in Medieval Funerary Rites: Chemical Fingerprints of Frankincense in Southern Belgian Incense Burners (2014) · cites this paper as [54]
In the citing paper
“Neotriterpenoids are formed from amyrins through a Nametkin rearrangement [54] and the Δ9(11),12 double bond constitutes the dehydrated form of Δ12 triterpenoids with an alcohol functionality on C-11 such as 11-hydroxyboswellic acids which are naturally present in frankincense [55].”
From Holy Smoke in Medieval Funerary Rites: Chemical Fingerprints of Frankincense in Southern Belgian Incense Burners (2014) · cites this paper as [54]
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Research works printed but not linked: 27
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Cited by
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Baeten, J., Deforce, K., Challe, S., De Vos, D., & Degryse, P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113142 · Cited by 43
Metadata
- Authors
- ten Haven, H. L., Peakman, T. M., & Rullkötter, J.
- Venue
- Geochimica et Cosmochimica Acta
- Publisher
- Elsevier BV
- Published
- 1992-05
- Volume
- 56
- Issue
- 5
- Pages
- 1993-2000
- ISSN
- 0016-7037
- Cited by
- 71
- References
- 0
- Language
- en
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