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- W2034137749 abstract "[structure: see text] A novel triterpenoid, 21,25-cyclodammar-20(22)-ene-3beta,24alpha-diol, has been isolated from Aglaia odorata. Its structure was elucidated on the basis of 1D- and 2D-NMR and MS spectra and then confirmed by X-ray diffraction. It represents a new type of natural five-membered-ring triterpenoid, named cyclodammarane. Its possible biopathway was that squalene-2,3;22,23-diepioxide was directly cyclized to form 24,25-epoxydammar-20(21)-en-3-ol, followed by protonation of the remaining 24,25-epoxide and the cation attacking 21(20) methylene to generate the E ring." @default.
- W2034137749 created "2016-06-24" @default.
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- W2034137749 date "2005-06-16" @default.
- W2034137749 modified "2023-10-16" @default.
- W2034137749 title "Compound Representatives of a New Type of Triterpenoid from <i>Aglaia </i><i>o</i><i>dorata</i>" @default.
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- W2034137749 doi "https://doi.org/10.1021/ol050805h" @default.
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