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Articolul precedent |
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SM ISO690:2012 MORĂRESCU (CHETRARU), Olga, GRINCO, Marina, KULCIŢKI, Veaceslav, BARBA, Alic, GARBUZ, Olga, GUDUMAK, V., GULYA, Aurelian, UNGUR, Nikon. A straightforward synthesis of natural oxygenated ent-kaurenoic acid derivatives. In: Synthetic Communications, 2020, nr. 9(17), pp. 1-11. ISSN 0039-7911. |
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Synthetic Communications | |||||||
Numărul 9(17) / 2020 / ISSN 0039-7911 /ISSNe 1532-2432 | |||||||
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Pag. 1-11 | |||||||
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Rezumat | |||||||
The paper presents the synthesis of some natural diterpenoids of ent-kauranic structure, starting from ent-kaur-16-en-19-oic acid, a natural diterpenoid readily available from the dried wastes of sunflower (Helianthus annuus L.). The reported ent-16α,17-dihydroxykauran-19-oic, ent-16α-hydroxy-17-acetoxykauran-19-oic and ent-16α,17-diacetoxykauran-19-oic acids have been previously isolated from different plant sources and showed diverse biological activities, including anti-HIV, anti-cancer and anti-Alzheimer properties. Their chemical synthesis has not been disclosed so far. Additional cytotoxicity studies of the obtained compounds revealed a remarkable cell proliferative effect of parent ent-kaur-16-en-19-oic acid and two of its synthetic derivatives, which is in line with recent pioneering studies in this area. |
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Cuvinte-cheie Allylic isomerization, bioactivity, cell proliferation, dihydroxilation, epoxidation, ent-kaurane, ent-16α-hydroxy-17-acetoxykauran-19-oic acid, ent-kaur-16-en-19-oic acid, ent-16α17-dihydroxylkauran-19-oic acid, ent-16α, 17-diacetoxykauran-19-oic acid, ent-16α17-epoxykauran-19-oic acid, ent-17-oxo-16R-kauran-19-oic acid, ent-17-hydroxykaur-15-en-19-oic acid. natural diterpenoids |
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