دورية أكاديمية
Three new 3-benzylbenzofuran-2-one derivatives from Homalium brachybotrys (Flacourtiaceae/Salicaceae s. l.)
| العنوان: | Three new 3-benzylbenzofuran-2-one derivatives from Homalium brachybotrys (Flacourtiaceae/Salicaceae s. l.) |
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| المؤلفون: | Mosaddik, M Ashik, Forster, Paul I, Waterman, Peter G |
| المصدر: | Southern Cross Plant Science |
| بيانات النشر: | ePublications@SCU |
| سنة النشر: | 2007 |
| المجموعة: | Southern Cross University: epublications@SCU |
| مصطلحات موضوعية: | Homalium brachybotrys, Flacourtiaceae/Salicaceae s.l, 5-Dihydroxybenzyl alcohol derivatives, Benzofuranone derivatives, Chemical taxonomy, Plant Sciences |
| الوقت: | 2 |
| الوصف: | Eight phenolic compounds, including two mixtures of two compounds, were isolated from the ethyl acetate extract of leaves and stems of Homalium brachybotrys. They were identified on the basis of spectroscopic data as quercetin-3-O-β-glucopyranoside, luteolin-7-O-β-glucopyranoside, 5,6-dihydro-6-β-glucopyranosyloxy-3-(hydroxyphenyl-methyl)-2(4H)-benzofuranone (cochinolide 6-O-β-glucopyranoside) (1), 2-(6-benzoyl-β-glucopyranosyloxy)-5-hydroxybenzyl alcohol (poliothrysoside) (2), 2-(β-glucopyranosyloxy)-5-hydroxybenzyl alcohol (salirepin) (3), 4,5-dihydro-7a-β-glucopyranosyloxy-3-(hydroxyphenylmethyl)-2(7aH)-benzofuranone (isocochinolide-7a-O-β-glucopyranoside) (4), 5,6-dihydro-3-(hydroxyphenylmethyl)-2(4H)-benzofuranone (6-deoxycochinolide) (5) and 3-benzylidine-6-hydroxy-2-benzofuranone (1'deoxy-4,5,6-dehydrocochinolide) (6). Benzofuranones (4), (5) and (6) are new natural products. The compounds isolated support the argument that Homalium is best placed in the Salicaceae s.l. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | unknown |
| العلاقة: | https://epubs.scu.edu.au/cpp_pubs/48Test; http://dx.doi.org/10.1080/14786410601130679Test |
| DOI: | 10.1080/14786410601130679 |
| الإتاحة: | https://doi.org/10.1080/14786410601130679Test https://epubs.scu.edu.au/cpp_pubs/48Test |
| رقم الانضمام: | edsbas.B6834B57 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1080/14786410601130679 |
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