Synthesis and antialgal effect of 2-substituted 5,6-dihydro-4,7-dithiaindane-1,3-diones

Ruzena Cizmarikova; Katarina Kralova; Pavol Hrnciar

doi:10.3390/ecsoc-4-01902

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Synthesis and antialgal effect of 2-substituted 5,6-dihydro-4,7-dithiaindane-1,3-diones

Ruzena Cizmarikova

^{*

1},

Katarina Kralova

²,

Pavol Hrnciar

¹ Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University, Kalinciakova 8, SK-832 32 Bratislava, Slovakia.,
² Institute of Chemistry, Faculty of Natural Sciences, Comenius University, Mlynska dolina CH-2, SK-842 15 Bratislava
³ Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, Mlynska dolina CH-2, SK-842 15 Bratislava

Published: 11 September 2000 by MDPI in The 4th International Electronic Conference on Synthetic Organic Chemistry session Bioorganic Chemistry and Natural Products

https://doi.org/10.3390/ecsoc-4-01902

Abstract: Derivatives of indane-1,3-diones are compounds showing interesting properties not only from theoretical view. Some 2-arylindane-1,3-diones are used as anticoagulants, dyes, polymerization modifiers and rodenticides. This study deals with synthesis, spectral and antialgal properties of new substituted 2-(5-aryl-2-thenylidene- or 2- furfurylidene)-5,6-dihydro-4,7-dithiaindane-1,3-diones II.

Keywords: cyclic 1,3-diketone, indane-1,3-dione , dithiaindane-1,3-dione, condensation reaction, antialgal effect, Chlorella vulgaris

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Ruzena Cizmarikova

Katarina Kralova

Pavol Hrnciar