Chemistry Journal of Moldova

DOI: dx.doi.org/10.19261/cjm.2008.03(2).10

Graphical Abstract: The method for synthetising new derivatives of the pinonic acid using, at the key step, the reaction of condensation with epichlorohydrin, has been elaborated. It has been shown that, in the presence of catalytic amount of tetrabutylammonium chloride, the reaction is directed towards the formation of etherchlorohydrin, which, later on, is easily transformed into epoxides as well as chloromethyldiketones with good overall yield.


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DOI: dx.doi.org/10.19261/cjm.2008.03(2).19

Graphical Abstract: This review deals the methods of preparation of the 11-bishomodrimane-8α-ol-12-one, a convenient synton for the synthesis of drimanic and bishomodrimanic compounds, including the biologically active ones. The triterpenic tetracyclic derivatives of the onoceranic range and the fragrance compounds with ambergris odour can be also obtained from this compound.


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DOI: dx.doi.org/10.19261/cjm.2008.03(1).10

Graphical Abstract: Ten steroidal saponins have been isolated form the seeds of Hyoscyamus niger L. for the first time and their structures have been elucidated. Seven saponins belong to spirostane series, two are furostane-type and one is pregnane glycoside. Hyoscyamosides B, C and C2 are new steroidal saponins, which have never been reported before in literature. Complete assignments of the 1H and 13C NMR chemical shifts for all these glycosides were achieved by means of one- and two-dimensional NMR techniques, including 1H–1H COSY, HSQC, HMBC and ROESY spectra.

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DOI: dx.doi.org/10.19261/cjm.2007.02(1).04

Graphical Abstract: A mixture of 7α- and 17-bromonorambreinolides was obtained on treatment of the mixture of isomeric methyl bicyclohomofarnesenoates, the norambreinolide transesterification product, with NBS and H2O2. The structure of 7α- and 17-bromonorambreinolides was elucidated on the basis of spectral data. The structure of 17-bromonorambreinolide was confirmed by its reduction with LiAlH4 into sclaradiol, and that of 7α-bromonorambreinolide by X-ray analysis.


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DOI: dx.doi.org/10.19261/cjm.2007.02(1).05

Graphical Abstract: Phytochemical analysis of the seeds of Hyocyamus niger L. (Solonaceae) resulted in the isolation of six steroidal glycosides, two furostanol (1, 2) and four spirostanol saponins (3, 4, 5, 6), which were found in this plant for the first time. The structures of these compounds were determined by detailed analysis of their spectral data, including two-dimensional NMR spectroscopy and MS spectroscopy. The antifungal activity of a crude steroidal glycoside extract, fractions of spirostanoles and individual glicosides was investigated in vitro against a panel of human pathogenic fungi, yeasts as well as dermatophytes and filamentous species.

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DOI: dx.doi.org/10.19261/cjm.2007.02(1).16

Graphical Abstract: 

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DOI: dx.doi.org/10.19261/cjm.2006.01(1).02

Graphical Abstract: Three steroidal glycosides of spirostane series have been isolated from the seeds of Hyoscyamus niger L.(Solanaceae). Their structures were determined on the basis of chemical evidence and extensive spectroscopic methods including one-dimensional, two-dimensional NMR and MS analysis. In the genus Hyoscyamus the given compounds have been found out for the first time.


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