Results 111 to 120 of about 1,572 (155)
Some of the next articles are maybe not open access.
Cardenolides from Erysimum cheiranthoides
Phytochemistry, 1996Three new cardiac glycosides were isolated along with two known cardenolides from the seeds of Erysimum cheiranthoides. The new ones were characterized by spectral methods as 16 beta-hydroxystrophanthidin (strophadogenin) 3-O-beta-glucopyranosyl-(1-->4)-beta-boiviopyranoside, strophadogenin 3-O-alpha-rhamnopyranosyl-(1-->4)-beta-digitoxopyranoside and ...
Z H, Lei +4 more
openaire +2 more sources
Cardenolides from Adonis aestivalis
Phytochemistry, 1992Four cardenolides were isolated for the first time from the aerial parts of Adonis aestivalis. The compounds were identified by spectrometry and for 3-epi-periplogenin, helveticoside also by comparison with authentic substances. Two new cardenolides were structurally elucidated: strophanthidin-3-O-beta-D-digitoxosido-alpha-L-cymarosido-be ta-D ...
B, Kopp +3 more
openaire +2 more sources
Cardenolides from Nierembergia aristata
Journal of Natural Products, 1995The EtOAc extract of the whole plant of the Argentinian species Nierembergia aristata showed significant cytotoxicity against eleven different cancer cell lines. In addition to several known compounds, bioassay-guided fractionation led to the isolation of three new cardenolides, 17-epi-11 alpha-hydroxy-6, 7-dehydrostrophanthidin-3-O-beta ...
R R, Gil +4 more
openaire +2 more sources
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
openaire +2 more sources
Cytotoxic cardenolides from Calotropis gigantea
Phytochemistry, 2021Sixteen cardiac glycosides, including five previously undescribed compounds, were extracted and purified from whole plants of Calotropis gigantea (L.). Spectroscopic data and electronic circular dichroism (ECD) analyses were used to determine their structures.
Yi-Lin, He +4 more
openaire +2 more sources
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
openaire +1 more source
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
Two cardenolides fromCalotropis procera
Magnetic Resonance in Chemistry, 1999Two cardiotonic glycosides were isolated from Calotropois procera; one of them (1) is a new natural product. Their structures were elucidated by extensive application of oneand two-dimensional 1H and 13C NMR spectroscopy. Copyright 1999 John Wiley & Sons, Ltd.
Atef G. Hanna +5 more
openaire +1 more source
ChemInform Abstract: CARDENOLIDES. I. RING D CLEAVAGE OF CARDENOLIDES
Chemischer Informationsdienst, 1982AbstractDie Einwirkung von Ozon auf die Cardadienolide (I) und nachfolgende reduktive Aufarbeitung führen überraschenderweise nicht zum Abbau des Butenolidringes, sondern nahezu ausschließlich zur D‐Ringspaltung unter Bildung der 14,1 S‐Seeocardenolide (IIa) und (IIb) bzw. (Ile).
E. COHNEN, K. WEDEMEIER, V. SINNWELL
openaire +1 more source
Chemischer Informationsdienst, 1981
AbstractDas Ausgangsprodukt für die Synthesen der Cardenolid‐Analogen (VII) bzw. (XI) ist das aus dem Iodketon (I) erhaltene (II).
F. THEIL, C. LINDIG, K. REPKE
openaire +1 more source
AbstractDas Ausgangsprodukt für die Synthesen der Cardenolid‐Analogen (VII) bzw. (XI) ist das aus dem Iodketon (I) erhaltene (II).
F. THEIL, C. LINDIG, K. REPKE
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source

