Structural revision of oleoacteoside and oleoechinacoside
@article{Machida2010StructuralRO, title={Structural revision of oleoacteoside and oleoechinacoside}, author={K. Machida and E. Matsuoka and M. Kikuchi}, journal={Natural Product Research}, year={2010}, volume={24}, pages={737 - 742} }
The structures of previously reported oleoacteoside and oleoechinacoside, both being caffeoyl phenylethanoid glycosides (acteoside, echinacoside) esterified with an oleoside 11-methyl ester, were revised by 2D-NMR spectral analysis.
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205 nm; flow rate, 1.5 mL min À1 ] to give 2 (35.0 mg). Fraction 1-6-4 was subjected to preparative HPLC [column, Cosmosil 5C18-AR
205 nm; flow rate, 1.5 mL min À1 ] to give crude 1, which was purified by preparative HPLC (column, TSK gel Amide-80
205 nm; flow rate, 1.5 mL min À1 ] to give crude 2, which was purified by preparative HPLC [column, TSK gel Amide-80
An amorphous powder
- FAB-MS: m/z 1173
Plant material The leaves of S. reticulata were collected near Sendai, Miyagi prefecture
- A voucher specimen is held in the laboratory of M. Kikuchi
UV (MeOH): max (log ") ¼ 220 (4.30)
- FAB-MS: m/z 1033 [M þ Na] þ . HR-FAB-MS: m/z 1033.3162 [M þ Na] þ (Calcd for C 46 H 58 O 25 Na: 1033.3190). 1 H-and 13 C-NMR