| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5161692 | Organic Geochemistry | 2013 | 7 Pages |
Abstract
⺠Transformation of triterpenoids during ozonation has been investigated. ⺠Various transformation products of β-amyrin and lupenone have been identified. ⺠No transformation product was detected for friedelin. ⺠Ozonation of β-amyrin proceeds via epoxydation, oxidation and ring-C opening reaction. ⺠Reaction of lupenone consists of de-alkylation, hydroxylation, epoxydation, oxidation.
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Authors
Kheng Soo Tay, Noorsaadah Abd. Rahman, Mhd. Radzi Bin Abas, Bernd R.T. Simoneit,