EventsThe 4th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Pavol Hrnciar, Katarina Kralova, Ruzena Cizmarikova, Synthesis and antialgal effect of 2-substituted 5,6-dihydro-4,7-dithiaindane-1,3-diones, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, 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 3
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
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
Via Ester Enolate Claisen Rearrangements To a Variety of Non-Proteinogenic Amino Acids
Facile and Efficient Synthesis of Functionalized Asymmetric Porphyrins with Organolithium Reagents