A straightforward synthesis of natural oxygenated ent-kaurenoic acid derivatives
Закрыть
Conţinutul numărului revistei
Articolul precedent
Articolul urmator
688 0
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, 2021, nr. 1(51), pp. 123-133. ISSN 0039-7911. DOI: https://doi.org/10.1080/00397911.2020.1821225
EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core
Synthetic Communications
Numărul 1(51) / 2021 / ISSN 0039-7911 /ISSNe 1532-2432

A straightforward synthesis of natural oxygenated ent-kaurenoic acid derivatives

DOI:https://doi.org/10.1080/00397911.2020.1821225

Pag. 123-133

Morărescu (Chetraru) Olga1, Grinco Marina1, Kulciţki Veaceslav1, Barba Alic1, Garbuz Olga23, Gudumak V.4, Gulya Aurelian2, Ungur Nikon1
 
1 Institute of Chemistry,
2 Moldova State University,
3 Institute of Zoology,
4 ”Nicolae Testemițanu” State University of Medicine and Pharmacy
 
 
Disponibil în IBN: 6 aprilie 2021


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.

Cuvinte-cheie
Allylic isomerization, bioactivity, cell proliferation, dihydroxilation, ent-16, ent-16α-hydroxy-17-acetoxykauran-19-oic acid, ent-16α17-dihydroxylkauran-19-oic acid, ent-16α17-epoxykauran-19-oic acid, ent-17-hydroxykaur-15-en-19-oic acid, ent-17-oxo-16R-kauran-19-oic acident-kaur-16-en-19-oic acid, ent-kaurane, epoxidation, natural diterpenoids, α17-diacetoxykauran-19-oic acid

Google Scholar Export

<meta name="citation_title" content="A straightforward synthesis of natural oxygenated ent-kaurenoic acid derivatives">
<meta name="citation_author" content="Morărescu (Chetraru) Olga">
<meta name="citation_author" content="Grinco Marina">
<meta name="citation_author" content="Kulciţki Veaceslav">
<meta name="citation_author" content="Barba Alic">
<meta name="citation_author" content="Garbuz Olga">
<meta name="citation_author" content="Gudumak V.">
<meta name="citation_author" content="Gulya Aurelian">
<meta name="citation_author" content="Ungur Nikon">
<meta name="citation_publication_date" content="2021/01/14">
<meta name="citation_journal_title" content="Synthetic Communications">
<meta name="citation_volume" content="51">
<meta name="citation_issue" content="1">
<meta name="citation_firstpage" content="123">
<meta name="citation_lastpage" content="133">
<meta name="citation_pdf_url" content="https://www.tandfonline.com/doi/abs/10.1080/00397911.2020.1821225">