scholarly journals New Guaianolide-Type Sesquiterpene Lactones from Inula verbascifolia

2013 ◽  
Vol 68 (5-6) ◽  
pp. 175-180
Author(s):  
Abou El-Hamd H. Mohamed ◽  
Hosam-Eldin H. Mahmoud ◽  
Fathy F. Abdellatif ◽  
Yousif S. Mohamed ◽  
Ahmed A. Ahmed
Keyword(s):  
Sesquiterpene Lactones ◽  
Spectroscopic Methods ◽  
H Nmr ◽  
Aerial Parts ◽  
C Nmr

The aerial parts of Inula verbascifolia afforded two new guaianolide-type sesquiterpene lactones. Their structures were determined by spectroscopic methods (IR, MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, HMQC, and HMBC).

Flavonoids from Achillea nobilis L.

2003 ◽  
Vol 58 (1-2) ◽  
pp. 11-16 ◽  
Author(s):  
Liselotte Krenn ◽  
Anca Miron ◽  
Enne Pemp ◽  
Ursula Petr ◽  
Brigitte Kopp
Keyword(s):  
Methyl Ether ◽  
Methanolic Extract ◽  
2D Nmr ◽  
Spectroscopic Methods ◽  
Esi Ms ◽  
H Nmr ◽  
Aerial Parts ◽  
Nmr Techniques ◽  
C Nmr

The detailed investigation of a methanolic extract of aerial parts of Achillea nobilis resulted in the isolation of 10 flavonoids. A new C-glycosylflavone, luteolin-6-C-apiofuranosyl-(1‴→2″)-glucoside, was isolated besides orientin, isoorientin, vitexin, isoschaftoside, luteolin- 7-O-β-glucuronide, luteolin-4′-O-β-glucoside and quercetin-3-O-methyl ether and two rare flavonolglycosides, quercetin-3-O-α-arabinosyl-(1‴→6″ )-glucoside and quercetin-3-O-methylether-7-O-β-glucoside. The structures were established either by comparison with authentic substances or by UV, 1H NMR and 13C NMR spectroscopic methods including 2ᴅ-NMR techniques and ESI-MS

Flavon- and Flavonolglycosides from Achillea pannonica Scheele

2001 ◽  
Vol 56 (7-8) ◽  
pp. 521-525 ◽  
Author(s):  
Denata Kasaj ◽  
Liselotte Krenn ◽  
Sonja Prinz ◽  
Antje Hüfner ◽  
Shi Shan Yuc ◽  
...  
Keyword(s):  
Methanolic Extract ◽  
2D Nmr ◽  
Flavonoid Glycosides ◽  
Spectroscopic Methods ◽  
Esi Ms ◽  
Aerial Parts ◽  
Nmr Techniques ◽  
Chemotaxonomic Study ◽  
First Time ◽  
C Nmr

The detailed investigation of a methanolic extract of aerial parts of Achillea pannonica SCHEELE. within a chemotaxonomic study led to the isolation of 6 flavonoid glycosides. Besides rutin, apigenin-7-O-glucopyranoside, luteolin-7-O-glucopyranoside, apigenin-7-O-rutinoside and acacetin-7-O-rutinoside, an unusual flavondiglucoside was isolated. Its structure was established by UV, 1HNMR and 13C NMR spectroscopic methods including 2D-NMR techniques and ESI-MS as luteolin-7,4′-O-β-diglucoside. This substance is reported for the first time in the genus Achillea. Chemotaxonomic aspects are discussed briefly

Flavonoids from Ficaria verna Huds.

2002 ◽  
Vol 57 (5-6) ◽  
pp. 440-444 ◽  
Author(s):  
Michał Tomczyk ◽  
Jan Gudej ◽  
Marek Sochacki
Keyword(s):  
Spectroscopic Methods ◽  
H Nmr ◽  
Flavonoid Compounds ◽  
Phytochemical Investigation ◽  
C Nmr ◽  
Ficaria Verna

A phytochemical investigation of the flowers and leaves of Ficaria verna Huds. (Ranunculaceae) yielded four additional known flavonoid compounds including: kaempferol 3-O-β-ᴅ- (6ʺ-α-ʟ-rhamnopyranosyl)-glucopyranoside (nicotiflorin), apigenin 8-C-β-ᴅ-glucopyranoside (vitexin), luteolin 8-C-β-ᴅ-glucopyranoside (orientin) and apigenin 8-C-β-ᴅ-(2ʺ-O-β-ᴅ-glucopyranosyl)- glucopyranoside (flavosativaside). The characterisation of these compounds was achieved by various chromatographic and spectroscopic methods (UV, 1H NMR, 13C NMR and MS).

A new ent-kaurane from the root extract of Chiococcaalba

1997 ◽  
Vol 75 (6) ◽  
pp. 801-804 ◽  
Author(s):  
Rocío Borges-Argáez ◽  
Leticia Medina-Baizabál ◽  
Filogonio May-Pat ◽  
Luis M. Peña-Rodríguez
Keyword(s):  
Antimicrobial Activity ◽  
Medicinal Plants ◽  
Crude Extract ◽  
Chemical Shifts ◽  
Root Extract ◽  
Spectroscopic Methods ◽  
Chemical Transformations ◽  
Bioactive Metabolite ◽  
H Nmr ◽  
C Nmr

A bioassay-guided purification of the methanolic crude extract obtained from the roots of Chiococcaalba (L.) Hitchc. resulted in the isolation of a new, bioactive, metabolite identified as ent-17-hydroxy-16α-kauran-3-one (1). Elucidation of the new structure was based on analyses of the results obtained from various spectroscopic methods (IR, MS, 1H NMR, and 13C NMR) and chemical transformations. The stereochemistry at C16 was assigned by comparing both the proton and carbon chemical shifts of C17 with those reported in the literature. The new kaurane showed weak antimicrobial activity when tested against Staphylococcusaureus. Keywords: medicinal plants, Chiococcaalba, Rubiaceae, kaurane, diterpene, antimicrobial.

Synthesis of 2-amino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydro- and -5,6,7,8-tetrahydroquinazoline derivatives

1985 ◽  
Vol 50 (7) ◽  
pp. 1602-1610 ◽  
Author(s):  
József Deli ◽  
Tamás Lóránd ◽  
Dezsö Szabó ◽  
András Földesi ◽  
Adolf Zschunke
Keyword(s):  
Spectroscopic Methods ◽  
H Nmr ◽  
C Nmr

Base-catalyzed reaction of 2,6-dibenzylidenecyclohexanone and alkylguanidines gave 2-alkylamino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydroquinazolines IVa-c, which were oxidized to 2-alkylamino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazolines Va-c. The acylamino (VIa-c, VIIa-d, IXa,b) and diacylamino derivatives (VIIIa,b) of the 2-amino-8-benzylidene-4-pheny]-3,4,5,6,7,8-hexahydroquinazoline (II), 2-amino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazoline (III) and compounds Va-c have also been prepared. These compounds having the E-configuration were converted into the Z isomers XIIa-e by photoisomerization. The structures were confirmed by spectroscopic methods (IR, 1H NMR, 13C NMR).

scholarly journals 9α-hydroxyparthenolide in Zoegea leptaurea subsp. mesopotamica (Czerep.) Rech. (Asteraceae)

2015 ◽  
Vol 61 (2) ◽  
pp. 7-13 ◽  
Author(s):  
Joanna Nawrot ◽  
Renata Dawid-Pać ◽  
Kinga Kaczerowska-Pietrzak ◽  
Maria Urbańska ◽  
Gerard Nowak
Keyword(s):  
Spectral Methods ◽  
H Nmr ◽  
Aerial Parts ◽  
C Nmr

Summary From the aerial parts of Zoegea leptaurea subsp. mesopotamica (Czerep.) Rech. (syn Zoegea mesopotamica Czerep.), 9α-hydroxyparthenolide was isolated. This compound was identified by spectral methods (1H NMR and 13C NMR). This research confirmed earlier indications about the presence of 4,5-epoxygermacranolides in the Zoegea L. genus. Thus, distinctive chemistry feature of plants in this taxon has chemotaxonomic implications.

Synthesis, Characterization and Photophysicochemical Properties of Zinc(Ii) Phthalocyanine With New Benzenesulfonamide Derivative Substituents

2021 ◽  
Author(s):  
Gülen Atiye Öncül ◽  
Ömer Faruk Öztürk ◽  
Mehmet Pişkin
Keyword(s):  
Elemental Analysis ◽  
Mass Spectra ◽  
Spectroscopic Methods ◽  
H Nmr ◽  
Maldi Tof Mass Spectra ◽  
New Type ◽  
Ft Ir ◽  
Photochemical Properties ◽  
Photocatalytic Applications ◽  
C Nmr

Abstract Novel (E)-4-((5-bromo-2-hydroxy-3-methoxybenzylidene)amino)-N-(pyridin-2-yl)benzenesulfonamide 1, (E)-4-((5-bromo-2-(3,4-dicyanophenoxy)-3-methoxybenzylidene)amino)-N-(pyridin-2-yl)benzene sulfonamide 2 and 2(3),9(10),16(17),23(24)-tetra-[(E)-4-((5-bromo-3-methoxy-2-(λ1-oxidanyl)benzyl idene)amino)-N-(pyridine-2-yl)benzenesulfonamide]phthalocyaninato zinc(II) phthalocyanine 3 were synthesized. Their (1-3) structures were illuminated with spectroscopic methods such as FT-IR, 1H NMR,13C NMR, UV–vis, MALDI-TOF mass spectra and also elemental analysis. The spectroscopic, photophysical and photochemical properties of the zinc(II) phthalocyanine 3 were investigated in dimethyl sulfoxide and its effects on the above mentioned properties were reported as a result of containing new type benzenesulfonamide derivatives as substituents. In addition, its above-mentioned properties were reported by comparing different species with those of their substituted and/or unsubstituted counterparts. The zinc(II) phthalocyanine 3 has photosensitizing abilities suitable and sufficient especially for photocatalytic applications.

A New Active Compound from Centaurea Species

2006 ◽  
Vol 61 (1-2) ◽  
pp. 44-46 ◽  
Author(s):  
Melek U. Dumlu ◽  
Elcin Gürkan
Keyword(s):  
Active Compound ◽  
Spectroscopic Data ◽  
Chemical Structure ◽  
Sesquiterpene Lactones ◽  
Antimicrobial Activities ◽  
H Nmr ◽  
Steroidal Compound ◽  
Antioxidant And Antimicrobial Activities ◽  
C Nmr

Abstract The extract containing sesquiterpene lactones of Centaurea iberica (Asteraceae) isolated was separated and a steroidal compound, which is stigmast-1,5-dien-3β-ol, was purified. The chemical structure was established based on spectroscopic data (UV, IR, MS, 1H NMR, 13C NMR). Both the extract and the compound showed significant antioxidant and antimicrobial activities

Identification of acyl groups occurring in sesquiterpene lactones: Proton and carbon-13 NMR study

1987 ◽  
Vol 52 (2) ◽  
pp. 453-475 ◽  
Author(s):  
Miloš Buděšínský ◽  
David Šaman
Keyword(s):  
Chemical Shifts ◽  
Sesquiterpene Lactones ◽  
Nmr Chemical Shifts ◽  
H Nmr ◽  
Nmr Parameters ◽  
Nmr Data ◽  
Nmr Study ◽  
C Nmr

Characteristic 1H NMR parameters of 88 acyl groups, hitherto found as ester substituents in natural sesquiterpenic lactones, were determined from the measured spectra as well as literature data. Characteristic 13C NMR chemical shifts for 45 acyl groups were obtained in the same way; for the remaining acyls with hitherto unknown 13C NMR data the values were calculated on the basis of semiempirical relationships.

Sesquiterpene Lactones from Achillea collina Becker

2002 ◽  
Vol 57 (7-8) ◽  
pp. 568-570 ◽  
Author(s):  
Elena Mustakerova ◽  
Milka Todorova ◽  
Elena Tsankova
Keyword(s):  
Sesquiterpene Lactones ◽  
Spectroscopic Methods ◽  
Aerial Parts

Aerial parts of Achillea collina afforded, in addition to five known sesquiterpene lactones two new germacranolides and one new eudesmanolide, the structures of which were elucidated by spectroscopic methods.

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