Results 111 to 120 of about 1,686 (179)
In vitro biological activities of silver nanoparticles using methanolic leaf extract of Plumeria rubra. [PDF]
Marukurti A +12 more
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Haplotype-resolved genome assembly of the upas tree (Antiaris toxicaria). [PDF]
Miao K +5 more
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Microbiome analysis of monarch butterflies reveals effects of development and diet. [PDF]
Sanaei E +9 more
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Nectar cardenolides and floral volatiles mediate a specialized wasp pollination system.
Burger H +5 more
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Cytotoxicity of cardenolides and cardenolide glycosides from Asclepias curassavica
Bioorganic and Medicinal Chemistry Letters, 2009A new cardenolide, 12beta,14beta-dihydroxy-3beta,19-epoxy-3alpha-methoxy-5alpha-card-20(22)-enolide (6), and a new doubly linked cardenolide glycoside, 12beta-hydroxycalotropin (13), together with eleven known compounds, coroglaucigenin (1), 12beta-hydroxycoroglaucigenin (2), calotropagenin (3), desglucouzarin (4), 6'-O-feruloyl-desglucouzarin (5 ...
Chen Qing +2 more
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Aldimines of Cardenolides and Cardenolide-Glycosides
Chemistry of Natural Compounds, 2005New aldimines were synthesized from the cardenolide strophantidin and cardenolide-glycosides erysimin and cymarin and included morpholine, nitrile, pyridine, furan, hydroxy- and methoxyphenyl, piperidine, and other derivatives. An effective modified method for synthesizing aldimines was proposed. 52 new compounds were synthesized. Their structures were
I. F. Makarevich +2 more
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Synthesis of cardenolide glycosides and putative biosynthetic precursors of cardenolide glycosides
Steroids, 1998A rapid and efficient procedure for glycosylation of steroids was established using a modified Koenigs-Knorr procedure. Peracetylated beta-glycosides were synthesized by reaction of cardenolides, various pregnanes and 23-nor-5,20(22)E-choldienic acid at room temperature with the peracetylated 1-bromo derivatives of D-glucose, D-galactose, D-fucose and ...
M, Luta, A, Hensel, W, Kreis
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Chemistry of Natural Compounds, 2005
3-Keto-derivatives of the cardenolides digitoxigenin and cardiogenin were prepared with subsequent conversion to new ketoimines (1–19, 24–44), the oxime (23), and for the first time to pure cardiogenin (14,16-dianhydrogitoxigenin, 20), its acetate (21), and cardiogenone (22). Their physicochemical properties were described.
I. F. Makarevich +2 more
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3-Keto-derivatives of the cardenolides digitoxigenin and cardiogenin were prepared with subsequent conversion to new ketoimines (1–19, 24–44), the oxime (23), and for the first time to pure cardiogenin (14,16-dianhydrogitoxigenin, 20), its acetate (21), and cardiogenone (22). Their physicochemical properties were described.
I. F. Makarevich +2 more
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Chemischer Informationsdienst, 1984
AbstractBehandeln der Cardenolide (I) mit NaH in DMF, anschließen de Zugabe der Alkylhalogenide (II) binnen fünf Minuten und Ansäuern der Ansätze liefern die Monoalkylderivate (III) als Hauptprodukte, daneben die Dialkylderivate (IV).
B. STRECKENBACH +4 more
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AbstractBehandeln der Cardenolide (I) mit NaH in DMF, anschließen de Zugabe der Alkylhalogenide (II) binnen fünf Minuten und Ansäuern der Ansätze liefern die Monoalkylderivate (III) als Hauptprodukte, daneben die Dialkylderivate (IV).
B. STRECKENBACH +4 more
openaire +1 more source

