Constituents of Olibanum Oil: Sesquiterpene Hydrocarbons

1970 ◽  
Vol 53 (5) ◽  
pp. 941-948
Author(s):  
Ronald L Yates ◽  
John A Wenninger

Abstract The sesquiterpene hydrocarbons of a commercial sample of olibanum oil were isolated and purified by a combination of techniques, including column chromatography, silver nitrate adduction, distillation, and preparative GLC. Most components were identified by their IR spectra. In some cases NMR spectra were used for identification. A total of 27 sesquiterpene hydrocarbons were identified: δ-elemene, α-cubebene, α-ylangene, α-copaene, β-bourbonene, α-gurjunene, β-elemene, transa- α-bergamotene, α-guaiene, β-ylangene, caryophyllene, β-copaene, aromadendrene, thujopsene, allo-aromadendrene, α–+ β-humulene, selina-4,ll-diene, γ-muurolene, α-muurolene,β-selinene, α-selinene, δ-cadinene, γ-cadinene, “cubenene”, β-cadinene, calamenene, and α-calacorene. The identification of β-ylangene and β1-cadinene are tentative.

1967 ◽  
Vol 50 (6) ◽  
pp. 1304-1313
Author(s):  
John A Wenninger ◽  
Ronald L Yates ◽  
Meyer Dolinsky

Abstract The sesquiterpene hydrocarbons of commercial samples of copaiba balsam and American cedarwood oils were separated by a combination of techniques including silver nitrate adduction, column chromatography on alumina, distillation, and gas chromatography. Components were identified by their infrared spectra. Of the 24 sesquiterpene hydrocarbons detected in copaiba balsam oil, 18 were identified as follows: δ-elemcne, copaene, β-cubebene, cyperene, α-bergamotene, β-elemene, caryophyllene,γ -elemene, β-farnesene, allo-aromadendrene, α-, β-humuIene, β-bisabolene, α-selinene, β-selinene, δ-cadinene, ar-curcumene, γ -cadinene, calamenene, and a-cubebene (tentatively identified). The following sesquiterpene hydrocarbons were identified in American cedarwood oil: β-eIemene, acedrene, caryophyllene, thujopsene, α-,βhumulene, "acorene," valencene, cuparene, a cuprenene, and two additional hydrocarbons (tentatively identified). Gas chromatographic retention data are reported for 27 of the sesquiterpene hydrocarbons isolated


1969 ◽  
Vol 52 (6) ◽  
pp. 1155-1161
Author(s):  
John A Wenninger ◽  
Ronald L Yates

Abstract Sesquiterpene hydrocarbons of opoponax oil were studied, using a combination of separat i on techniques which included column chromatography on alumina, silver nitrate adduction, and gas chromatography. Compounds isolated were identified by IR and NMR spectroscopy. Eighteen sesquiterpene hydrocarbons were identified as follows: Δ-elemene, α-cubebene, α-copaene, cis-α-bergamotene, β-elemene, α-santalene, trans-α-bergamotene, caryophyllene, γ-elemene, epi-β-santalene, β-santalene, humulene, γ-muurolene, trans-α-bisabolene, β-bisabolene, ar-curcumene, Δ-cadinene, and γ-cadinene. The major products obtained when hydrocarbons are regenerated from bisabolene trihydrochloride, using sodium acetate and acetic acid as reagents, were also characterized and identified as cis-α-bisabolene and β-bisabolene.


1996 ◽  
Vol 3 (3) ◽  
pp. 117-122
Author(s):  
M. B. de Oliveira ◽  
J. Miller ◽  
R. E. Banks ◽  
L. R. Kelland ◽  
C. A. McAuliffe ◽  
...  

Two new platinum(II) complexes have been synthesized and their anti-tumour and anti-HIV activities have been evaluated.The new complexes are: (i) cis-tetrafluorophthalate-ammine-morpholine-platinum(II) or MMF3 and (ii) cis-tetrafluorophthalate- ammine-piperidine-platinum(II) or MPF4. They were characterized by elemental analysis, IR spectra and H1 and C13 NMR spectra.They were tested against five human ovarian carcinoma cell lines, viz., CH1, CH1cisR, A2780, A2780cisR and SKOV-3. They were less active than cis-platin and showed cross-resistance with cis-platin in the CH1cisR and A2780cisR acquired resistance lines.They were also tested for possible anti-HIV activity using the HIV-I IIIB virus and C8166 cells, but they were inactive compared with AZT.


1964 ◽  
Vol 47 (4) ◽  
pp. 688-692
Author(s):  
Antoine Major

Abstract A method is described which will quantitatively determine 0.1 mg oxyphenisatin or the diacetate in various pharmaceutical preparations. After removal of interferences by organic solvent extractions from aqueous solution and partition column chromatography, the reaction of oxyphenisatin (diacetate) with silver nitrate in alcoholic sodium hydroxide solution produces a violet solution, which follows Beer’s law (1—15 μg per ml). The method was satisfactorily applied to the assay of commercial tablets, liquids, and powders with recoveries, as per cent found of declared, in the range 95—101%.


Synthesis ◽  
1973 ◽  
Vol 1973 (06) ◽  
pp. 362-363 ◽  
Author(s):  
Bernard LOEV ◽  
Paul E. BENDER ◽  
Robert SMITH

1991 ◽  
Vol 46 (1-2) ◽  
pp. 12-18 ◽  
Author(s):  
Antonio G . González ◽  
Jaime Bermejo Barrera ◽  
Elsa Ma Rodríguez Pérez ◽  
Consuelo E. Hernández Padrón

Column chromatography of the acetone extract of the lichen Cladina macaronesica (Sephadex LH-20, silica gel and silver nitrate-im pregnated silica gel) afforded eight triterpenes identified by chemical and spectral m eans. α-Amyrenone, lupenone, taraxerol, taraxerone and /so-arborinol acetate were isolated for the first time from lichens and (-)-usnic acid and five mononuclear phenolic compounds were also obtained, four for the first time as natural products. The possible transformation of perlatolic acid into these phenolic compounds is briefly outlined.


Jurnal Kimia ◽  
2016 ◽  
Author(s):  
Ni Made Dwi Desiyanti ◽  
I Made Dira Swantara ◽  
I Putu Sudiarta

The study of isolation and identification of the active compounds of soursop (Annona muricata L.) leave extract were conducted . The metabolite extraction was conducted using maceration method with 96 % ethanol. The ethanol extract was used to test the mortility of aphid (Myzus persicae S.), with LC50 of 100 ppm. The n-hexane, chloroform, and n-buthanol were used to fractionate the ethanol extract. The mortality test of those three extracts showed the LC50 of 545.12 ppm, 136.26 ppm and 117.73 ppm, respectively. The n-butanol extract was separated using silica gel column chromatography with chloroform: ethanol: water (5:4:1), as the mobile phase. The fractions resulted were FI, FII, FIII, FIV and FV. The mortality test indicated that FII was the best with LC50 of 596.48 ppm. The FII was purified using silica gel column chromatography, resulting three fractions (FII.1, FII.2 and FII.3).  The mortality test of those fractions indicated that FII.2 showed the best result with LC50 of 601.17 ppm. The UV-Vis and IR spectra showed that FII.2 fraction contained flavonoides under the flavonon family.


1962 ◽  
Vol 39 (3) ◽  
pp. 385-394 ◽  
Author(s):  
Wilhelm Dirscherl ◽  
Helmut Thomas ◽  
Herbert Schriefers

ABSTRACT In rat livers perfused with 3-methoxy-4-hydroxy-mandelic acid, formerly believed to be the endproduct of the metabolism of adrenaline and noradrenaline, three metabolites were detected by paper chromatography. After further purification by column chromatography, one of these substances was identified by melting point, shape of crystals, UV- and IR-spectra as vanillic acid. Perfusion with vanillic acid yielded only one metabolite in very small quantities. Because of its properties it is assumed to be a conjugate of vanillic acid. Hence vanillic acid, isolated in 1959 from human urine by Dirscherl & Schmidtmann, is the actual endproduct of the metabolism of adrenaline and noradrenaline.


1971 ◽  
Vol 26 (2) ◽  
pp. 75-78 ◽  
Author(s):  
Herbert W. Roesky ◽  
Graalf Remmers

By reaction of N-sulfuroxideimides with phosphorus-pentabromide the compounds R-SO2NPBr3 (R = CH3 , CF3 , C6H5, p-Cl-C6H4, and p-CH3C6H4) were prepared. Reactions of hexamethyldisilazane and N- (dimethyl) -trimethylsilylamide resulted in the formation of R-SO2NPBr2N (CH3)2, (R = CH3, C6H5), and R-SO2NPBr2NHSi(CH3)3 (R = CF3, p-CH3-C6H4). The properties and the chemical behavior of these compounds are described. Results of IR-spectra, as well as 31P-, 19F-, and 1H-NMR-spectra and elemental analysis characterize the compounds.


1970 ◽  
Vol 53 (5) ◽  
pp. 949-963 ◽  
Author(s):  
John A Wenninger ◽  
Ronald L Yates

Abstract An additional 24 high resolution IR spectra of naturally occurring sesquiterpene hydrocarbons are presented. Compounds were isolated from essential oils and purified by GLC techniques. The purity of each compound was checked by capillary column GLC. Infrared spectra of the following compounds are included: aromadendrene, allo-aromadendrene, cis-α-bergamotene, trans-β-bergamotene, cisa-α-bisabolene, trans-α-bisabolene, “α2-bisabolene“, cis-γ-bisabolene, β-cadinene, β1-cadinene, α-calacorene, chamazulene, β-chamigrene, “cubenene“, α-himachalene, β-himachalene, longicyclene, longifolene, α-muurolene, γ-muurolene, γ-patchoulene, epi-β-santalene, selina-4,ll-diene, and ylangene.


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