Zobrazeno 1 - 10
of 17
pro vyhledávání: '"neomarinone"'
Autor:
Khadija Hassan, Clara Chepkirui, Natalia Andrea Llanos-López, Josphat C. Matasyoh, Cony Decock, Yasmina Marin-Felix, Marc Stadler
Publikováno v:
Biomolecules, Vol 12, Iss 6, p 755 (2022)
A mycelial culture of the African basidiomycete Echinochaete cf. brachypora was studied for biologically active secondary metabolites, and four compounds were isolated from its crude extract derived from shake flask fermentations, using preparative h
Externí odkaz:
https://doaj.org/article/670936d2fdf44d09bd28429c92dd64a5
Akademický článek
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Publikováno v:
Chemistry - A European Journal. 15:910-916
The first total synthesis of (+)-neomarinone has been achieved by following a concise and convergent route using methyl (R)-lactate and (R)-3-methylcyclohexanone as chiral building blocks. Key steps of the synthesis are the stereocontrolled formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dadbaf422002ff47e0b1393516b1df93
https://doi.org/10.1002/chem.200802021
https://doi.org/10.1002/chem.200802021
Publikováno v:
Tetrahedron Letters. 48:6493-6495
A practical and efficient stereoselective synthesis of the side chain of neomarinone is reported. The synthesis was achieved in six steps (41% overall yield) from 2-methyl-2-cyclohexenone. The key step is a novel stereoselective 1,4-conjugate additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6498e2aec1cfeaa2c871e234638850b
https://doi.org/10.1016/j.tetlet.2007.07.064
https://doi.org/10.1016/j.tetlet.2007.07.064
Publikováno v:
ChemInform. 40
The first total synthesis of (+)-neomarinone has been achieved by following a concise and convergent route using methyl (R)-lactate and (R)-3-methylcyclohexanone as chiral building blocks. Key steps of the synthesis are the stereocontrolled formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::648a8830c22f2ed5aa8bacfe504b6f9d
https://doi.org/10.1002/chin.200920192
https://doi.org/10.1002/chin.200920192
Publikováno v:
ChemInform. 39
A practical and efficient stereoselective synthesis of the side chain of neomarinone is reported. The synthesis was achieved in six steps (41% overall yield) from 2-methyl-2-cyclohexenone. The key step is a novel stereoselective 1,4-conjugate additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66645e47458c317b7c50e31a728b1641
https://doi.org/10.1002/chin.200801211
https://doi.org/10.1002/chin.200801211
Publikováno v:
Antonie van Leeuwenhoek. 87(1)
Drug discovery relies on the generation of large numbers of structurally diverse compounds from which a potential candidate can be identified. To this end, actinomycetes have often been exploited because of their ability to biosynthesize an impressiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bc0ece0dc4367c98ff28bcafa08acd9
https://pubmed.ncbi.nlm.nih.gov/15726291
https://pubmed.ncbi.nlm.nih.gov/15726291
Publikováno v:
ChemInform. 35
[reaction: see text] The biosynthesis of the meroterpenoid neomarinone from a marine actinomycete was probed through feeding experiments with (13)C-labeled precursors. NMR characterization of [U-(13)C(6)]glucose-enriched neomarinone led to the struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::189a9c9a0a7c982de86a2dcf49cafd12
https://doi.org/10.1002/chin.200413140
https://doi.org/10.1002/chin.200413140
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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