Doprinos istraživanju slobodnih i glikozidno vezanih isparljivih spojeva od 2001. do 2006.

Kemija u Industriji. 2007;56(04):199-207


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Journal Title: Kemija u Industriji

ISSN: 0022-9830 (Print); 1334-9090 (Online)

Publisher: Croatian Society of Chemical Engineers

Society/Institution: Croatian Society of Chemical Engineers

LCC Subject Category: Science: Chemistry

Country of publisher: Croatia

Language of fulltext: English, Croatian

Full-text formats available: PDF



Jerković, I.


Blind peer review

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Time From Submission to Publication: 24 weeks


Abstract | Full Text

This review paper presents a contribution to the research of free and glycosidically bound volatiles in the 2001-2006 period obtained by work in the Department of Organic Chemistry, Faculty of Chemistry and Technology, University of Split, Croatia. Many terpene structures, phenylpropane derivatives (Fig. 6), as well as aliphatic hydrocarbons, alcohols, carbonyls, fatty acids and others were identified (Fig. 5). The chemotypes of Origanum vulgare ssp. hirtum, Artemisia absinthium and Myrtus communis were determined and some uninvestigated or insufficiently investigated plants (Micromeria juliana, Sequaoiadendron giganteum, Populus nigra, Prunus mahaleb, Ailanthus altissima and others) were analyzed. A newly developed method of co-distillation enabled isolation of unstable volatile compounds without formation of artefacts (Fig. 1).The volatile aglycones liberated by enzymatic hydrolysis of the corresponding glycosides were aliphatic and phenylpropanoic derivatives, as well as monoterpenes, sesquiterpenes and others (Fig. 7). Only partial similarity was observed in the composition of volatile aglycones and corresponding free volatiles of the same plant.Furthermore, glucosides of ubiquitous monoterpene and aliphatic alcohols and phenols were prepared by Koenigs-Knorr glucosylation (Fig. 8), by enzymatic condensation and transglucosidation from cellobiose (Fig. 11) and by direct glucosylation with FeCl<sub>3</sub> (Fig. 13). The products were characterized by GC-MS analysis of prepared tetraacetyl glucosides. Fragment ion characteristics of the aglucone moiety were present in all mass spectra, along with the fragments obtained from acetylated glucose (Fig. 12 and Fig. 14). Acetylated glucosides were separable on the HP-101 column, Fig. 9 (even diastereomeric tetraacetyl ß-glucosides of enantiomeric alcohols, Fig. 10).