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Results: 1-9 |
Results: 9
New approach to synthesis of N-substituted 9-amino/iminoacridines with important fluorescence properties
Authors: Kristian, P Bernat, J Imrich, J Sedlak, E Alfoldi, J Cornanic, M
Citation: P. Kristian et al., New approach to synthesis of N-substituted 9-amino/iminoacridines with important fluorescence properties, HETEROCYCLE, 55(2), 2001, pp. 279-290
The variability of (Z)- and (E)-2-beta-D-glucopyranosyloxy-4-methoxycinnamic acids and apigenin glucosides in diploid and tetraploid Chamomilla recutita
Authors: Repcak, M Pastirova, A Imrich, J Svehlikova, V Martonfi, P
Citation: M. Repcak et al., The variability of (Z)- and (E)-2-beta-D-glucopyranosyloxy-4-methoxycinnamic acids and apigenin glucosides in diploid and tetraploid Chamomilla recutita, PLANT BREED, 120(2), 2001, pp. 188-190
Umbelliferone, a stress metabolite of Chamomilla recutita (L.) Rauschert
Authors: Repcak, M Imrich, J Franekova, M
Citation: M. Repcak et al., Umbelliferone, a stress metabolite of Chamomilla recutita (L.) Rauschert, J PLANT PHY, 158(8), 2001, pp. 1085-1087
Unexpected formation of a spiro acridine and fused ring system from the reaction between an N-acridinylmethyl-substituted thiourea and bromoacetonitrile under basic conditions
Authors: Klika, KD Bernat, J Imrich, J Chomca, I Sillanpaa, R Pihlaja, K
Citation: Kd. Klika et al., Unexpected formation of a spiro acridine and fused ring system from the reaction between an N-acridinylmethyl-substituted thiourea and bromoacetonitrile under basic conditions, J ORG CHEM, 66(12), 2001, pp. 4416-4418
Quantitative evaluation of the main sesquiterpenes and polyacetylenes of Chamomilla recutita essential oil by high-performance liquid chromatography
Authors: Repcak, M Imrich, J Garcar, J
Citation: M. Repcak et al., Quantitative evaluation of the main sesquiterpenes and polyacetylenes of Chamomilla recutita essential oil by high-performance liquid chromatography, PHYTOCH AN, 10(6), 1999, pp. 335-338
A convenient synthesis of polyfunctionally substituted 2 ',2 '-bis(ethoxycarbonyl)methylene-5 '-methoxycarbonyl(cyano)spiro[dihydroacridine-9(10H),4 '-thiazolidines]
Authors: Bernat, J Chomca, I Kristian, P Pihlaja, K Klika, KD Imrich, J
Citation: J. Bernat et al., A convenient synthesis of polyfunctionally substituted 2 ',2 '-bis(ethoxycarbonyl)methylene-5 '-methoxycarbonyl(cyano)spiro[dihydroacridine-9(10H),4 '-thiazolidines], HETEROCYCLE, 51(1), 1999, pp. 137-140
A convenient synthesis of polyfunctionally substituted (acridin-9-yl)imino-1,3-thiazolidin-4-ones and spiro[9,10-dihydroacridine-9,4 '-thiazolidines]
Authors: Kristian, P Chomca, I Bernat, J Imrich, J
Citation: P. Kristian et al., A convenient synthesis of polyfunctionally substituted (acridin-9-yl)imino-1,3-thiazolidin-4-ones and spiro[9,10-dihydroacridine-9,4 '-thiazolidines], CHEM PAP-CH, 53(1), 1999, pp. 49-52
Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert
Authors: Repcak, M Svehlikova, V Imrich, J Pihlaja, K
Citation: M. Repcak et al., Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert, BIOCH SYST, 27(7), 1999, pp. 727-732
Synthesis of acetylcholinesterase inhibitors on the basis of 9-isothiocyanato-1,2,3,4-tetrahydroacridine: 2-[1,2,3,4-tetrahydroacridin-9-yl)imino]-3-substituted 1,3-thiazolidin-4-ones
Authors: Kristian, P Hamul'akova, S Bernat, J Imrich, J Voss, G Busova, T
Citation: P. Kristian et al., Synthesis of acetylcholinesterase inhibitors on the basis of 9-isothiocyanato-1,2,3,4-tetrahydroacridine: 2-[1,2,3,4-tetrahydroacridin-9-yl)imino]-3-substituted 1,3-thiazolidin-4-ones, HETEROCYCLE, 49, 1998, pp. 197-204
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