Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Eusiderin"'
Autor:
Madyawati Latief, Anis Yohana Chaerunisaa, Muhaimin Muhaimin, Didin Mujahidin, Syamsurizal Syamsurizal, Rahmi Iskandar
Publikováno v:
Current Organocatalysis. 7:44-54
Background:Eusiderin A is a neolignan derivate, which makes up the majority of the secondary metabolite of Eusideroxylon zwageri. It has been reported as a potent biopesticide and antifungal agent. Previous studies on the oxidation of terminal methyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ab216a24d90a1a5acd82ac436dd75f6
https://doi.org/10.2174/2213337206666190730144041
https://doi.org/10.2174/2213337206666190730144041
Publikováno v:
Journal of Natural Products. 81:2630-2637
1,4-Benzodioxane lignans are a class of bioactive compounds that have received much attention through the years. Herein research pertaining to both 1,4-benzodioxane flavonolignans and 1,4-benzodioxane neolignans is presented. A novel synthesis of bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad62551f19ad72c8f72e32fefe637f8b
https://doi.org/10.1021/acs.jnatprod.8b00416
https://doi.org/10.1021/acs.jnatprod.8b00416
Akademický článek
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Akademický článek
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Publikováno v:
Chemistry of Natural Compounds. 45:356-359
Two new lignans were isolated with two other known compounds, eusiderin A and eusiderin I, from Eusideroxylon zwageri (billian). The two new lignans have isomeric structure. The structures of the new lignans were determined to be (2R,3R,4S)-2,3-dimet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3029e297a35245e130401157c99b6e86
https://doi.org/10.1007/s10600-009-9346-6
https://doi.org/10.1007/s10600-009-9346-6
Publikováno v:
Journal of the Chinese Chemical Society. 48:59-63
(±)-Eusiderin G and (±)-Eusiderin M were first synthesized from pyrogallol, in which the Claisen Rearrangement was used to afford two important C6-C3 units.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e6232d031624e6cf297f2a9158252e2
https://doi.org/10.1002/jccs.200100011
https://doi.org/10.1002/jccs.200100011
Publikováno v:
Synthetic Communications. 31:861-867
(±)-Eusiderin K and (±)-Eusiderin J were first synthesized from pyrogallol, in which the Claisen Rearrangement was used to afford two important C6-C3 units.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2fec71cbbfdefc48564a25d5c48b85e
https://doi.org/10.1081/scc-100103321
https://doi.org/10.1081/scc-100103321
Autor:
Li Ming Yang Kuo, Susan L. Morris-Natschke, Hsiu O. Ho, Zhi Hu Lin, Yao-Haur Kuo, Kuo Hsiung Lee, Hung Tse Huang, Li Jie Zhang, Chia Ching Liaw, Hui Ling Cheng
Publikováno v:
Journal of natural products. 76(4)
Four new 8,8',7,2'-lignans, (+)-ovafolinin B-9'-O-β-d-glucopyranoside (1), (-)-ovafolinin B-9'-O-β-d-glucopyranoside (2), (+)-ovafolinin E-9'-O-β-d-glucopyranoside (3), and (-)-ovafolinin E-9'-O-β-d-glucopyranoside (4), two neolignans, eusiderin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c15c59be8d13a92797f4af700274064
https://pubmed.ncbi.nlm.nih.gov/23540981
https://pubmed.ncbi.nlm.nih.gov/23540981
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50913b50c55ea0c80250ee723101382d
https://doi.org/10.1002/chin.199329265
https://doi.org/10.1002/chin.199329265
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dd50658b039861aab798285151a7364
https://doi.org/10.1002/chin.199522271
https://doi.org/10.1002/chin.199522271