| DC Field | Value | Language |
|---|
| dc.contributor.author | Kopak, Nazar | |
| dc.contributor.author | Stasevych, Maryna | |
| dc.contributor.author | Zvarych, Viktor | |
| dc.contributor.author | Deniz, Nahide Gulsah | |
| dc.contributor.author | Sayil, Cigdem | |
| dc.contributor.author | Ozyurek, Mustafa | |
| dc.contributor.author | Guclu, Kubilya | |
| dc.contributor.author | Vovk, Mykhailo | |
| dc.contributor.author | Novikov, Volodymyr | |
| dc.coverage.temporal | 23–25 листопада 2017 року | |
| dc.coverage.temporal | 23–25 November, 2017 | |
| dc.date.accessioned | 2018-04-12T13:07:12Z | - |
| dc.date.available | 2018-04-12T13:07:12Z | - |
| dc.date.created | 2017-12-23 | |
| dc.date.issued | 2017-12-23 | |
| dc.identifier.citation | Anthraquinonylhydrazones of α-active ketones and β-carbonyl-containing compunds: synthesis and antioxidant activity / Nazar Kopak, Maryna Stasevych, Viktor Zvarych, Nahide Gulsah Deniz, Cigdem Sayil, Mustafa Ozyurek, Kubilya Guclu, Mykhailo Vovk, Volodymyr Novikov // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 32–33. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)). | |
| dc.identifier.isbn | 978-966-941-108-2 | |
| dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/40532 | - |
| dc.description.abstract | An effective method for the synthesis of
1-anthraquinonyl hydrazones containing the acyl- and/or
ethoxycarbonyl, carbo- and heterocyclic fragments in the
ylidene moiety has been shown, which are convenient reagents
for further chemical transformations. Investigation of the
antioxidant activity of hydrazones has allowed to identify
promising compounds that can be suggested for further
research as antioxidant substances. | |
| dc.format.extent | 32-33 | |
| dc.language.iso | en | |
| dc.publisher | Видавництво Львівської політехніки | |
| dc.publisher | Lviv Polytechnic Publishing House | |
| dc.relation.ispartof | Litteris et Artibus : матеріали, 2017 | |
| dc.relation.ispartof | Litteris et Artibus : proceedings, 2017 | |
| dc.subject | 9 10-anthraquinone | |
| dc.subject | diazonium salt | |
| dc.subject | hydrazone | |
| dc.subject | α-active ketones | |
| dc.subject | β-carbonylcontaining compunds | |
| dc.subject | antioxidant activity | |
| dc.title | Anthraquinonylhydrazones of α-active ketones and β-carbonyl-containing compunds: synthesis and antioxidant activity | |
| dc.type | Conference Abstract | |
| dc.rights.holder | © Національний університет “Львівська політехніка”, 2017 | |
| dc.contributor.affiliation | Lviv Polytechnic National University | |
| dc.contributor.affiliation | Istanbul University, TURKEY, Istanbul | |
| dc.contributor.affiliation | Division of Analytical Chemistry, TURKEY, Istanbul | |
| dc.contributor.affiliation | Department of Mechanisms of Organic Reactions, UKRAINE, Kyiv | |
| dc.format.pages | 2 | |
| dc.identifier.citationen | Anthraquinonylhydrazones of α-active ketones and β-carbonyl-containing compunds: synthesis and antioxidant activity / Nazar Kopak, Maryna Stasevych, Viktor Zvarych, Nahide Gulsah Deniz, Cigdem Sayil, Mustafa Ozyurek, Kubilya Guclu, Mykhailo Vovk, Volodymyr Novikov // Litteris et Artibus : proceedings, 23–25 November, 2017. — Lviv : Lviv Polytechnic Publishing House, 2017. — P. 32–33. — (6th International academic conference «Chemistry & chemical technology 2017» (CCT-2017)). | |
| dc.relation.references | [1] N. Belskaya, W. Dehaen, V. Bakulev, “Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions,” Arkivoc, vol. I, pp. 275-332, 2010. | |
| dc.relation.references | [2] R. Ali, A. Marella, T. Alam, R. Naz, M. Akhter, Md. Shaquiquzzaman, R. Saha, O. Tanwar, M. Alam, J. Hooda, “Review of biological activities of hydrazones,” Indones. J. Pharm., vol. 23, pp. 193-202, 2012. | |
| dc.relation.references | [3] Q.A. Acton, Ed., Anthraquinones. Advances in Research and Application. Atlanta : Scholarly Editions,2013. | |
| dc.relation.references | [4] S. Arai, S. Kato, M.B. Hida, “Anthraquinone pharmaceutical compounds and uses therefor,” J. Chem. Soc. Jpn., vol. 58, p. 1458, 1985. | |
| dc.relation.references | [5] I. Antonini, P. Polucci, D. Cola, G. Palmieri, S. Martelli, M. Bon-temps-Gracz, “Synthesis of 9,10-anthraquinone monoalkylaminoalkylhydrazones as potential antitumor drugs,” Farmaco, vol. 48, pp. 1641-1648, 1993. | |
| dc.relation.references | [6] V.A. Loskutov, “Reaction of anthrone and its 1-and 4- substituted derivatives with sulfur in the presence of nucleophiles,” Russ. J. Org. Chem., vol. 36, pp. 1478-1481, 2000. | |
| dc.relation.references | [7] M. Regitz, “Reaktionen aktiver Methylen-verbindungen mit Aziden, III. Über die Diazo-, Azino- und Triphenylphosphazino-Derivate des Anthrons und Thioxanthen-S-dioxids,” Chem. Ber., vol. 97, pp. 2742-2754, 1964. | |
| dc.relation.references | [8] S.L. Vorob’eva, V.N. Buyanov, I.I. Levina, N.N. Suvorov, “Naphthindoles. 2. Naphtho[2,3-e]indole-4,9- diones and naphtho[2,3-f]indole-5,10-diones,” Chem. Heterocycl. Compd., vol. 25, pp. 646–649, 1989. | |
| dc.relation.references | [9] K. MeeKyoung, D.F. Wiemer, “EDC-mediated condensations of 1-chloro-5-hydrazino-9, 10-anthracenedione,1-hydrazino-9,10-anthracenedione, and the corresponding anthrapyrazoles,” Tetrahedron Lett., vol. 45,pp. 4977- 4980, 2004. | |
| dc.relation.references | [10]V. Zvarych, M. Stasevych, V. Lunin, N.G. Deniz, C. Sayil, M. Ozyurek, K. Guclu, M. Vovk, V. Novikov, “Synthesis and investigation of antioxidant activity of the dithiocarbamate derivatives of 9,10-anthracenedione”, Monatsh. Chem., vol. 147, pp. 2093-2101,2016. | |
| dc.relation.references | [11]R. Apak, K. Güçlü, M. Özyürek, S.E. Karademir, “Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method,” J. Agric. Food Chem., vol.52,pp.7970-7981, 2004. | |
| dc.relation.references | [12]B. Bekdeşer, M. Özyürek, K. Güçlü, F. Üstün Alkan, R. Apak,“Development of a new catalase activity assay for biological samples using optical CUPRAC sensor,” Spectrochim. Acta Part A, vol. 132, pp. 485-490, 2014. | |
| dc.relation.referencesen | [1] N. Belskaya, W. Dehaen, V. Bakulev, "Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions," Arkivoc, vol. I, pp. 275-332, 2010. | |
| dc.relation.referencesen | [2] R. Ali, A. Marella, T. Alam, R. Naz, M. Akhter, Md. Shaquiquzzaman, R. Saha, O. Tanwar, M. Alam, J. Hooda, "Review of biological activities of hydrazones," Indones. J. Pharm., vol. 23, pp. 193-202, 2012. | |
| dc.relation.referencesen | [3] Q.A. Acton, Ed., Anthraquinones. Advances in Research and Application. Atlanta : Scholarly Editions,2013. | |
| dc.relation.referencesen | [4] S. Arai, S. Kato, M.B. Hida, "Anthraquinone pharmaceutical compounds and uses therefor," J. Chem. Soc. Jpn., vol. 58, p. 1458, 1985. | |
| dc.relation.referencesen | [5] I. Antonini, P. Polucci, D. Cola, G. Palmieri, S. Martelli, M. Bon-temps-Gracz, "Synthesis of 9,10-anthraquinone monoalkylaminoalkylhydrazones as potential antitumor drugs," Farmaco, vol. 48, pp. 1641-1648, 1993. | |
| dc.relation.referencesen | [6] V.A. Loskutov, "Reaction of anthrone and its 1-and 4- substituted derivatives with sulfur in the presence of nucleophiles," Russ. J. Org. Chem., vol. 36, pp. 1478-1481, 2000. | |
| dc.relation.referencesen | [7] M. Regitz, "Reaktionen aktiver Methylen-verbindungen mit Aziden, III. Über die Diazo-, Azino- und Triphenylphosphazino-Derivate des Anthrons und Thioxanthen-S-dioxids," Chem. Ber., vol. 97, pp. 2742-2754, 1964. | |
| dc.relation.referencesen | [8] S.L. Vorob’eva, V.N. Buyanov, I.I. Levina, N.N. Suvorov, "Naphthindoles. 2. Naphtho[2,3-e]indole-4,9- diones and naphtho[2,3-f]indole-5,10-diones," Chem. Heterocycl. Compd., vol. 25, pp. 646–649, 1989. | |
| dc.relation.referencesen | [9] K. MeeKyoung, D.F. Wiemer, "EDC-mediated condensations of 1-chloro-5-hydrazino-9, 10-anthracenedione,1-hydrazino-9,10-anthracenedione, and the corresponding anthrapyrazoles," Tetrahedron Lett., vol. 45,pp. 4977- 4980, 2004. | |
| dc.relation.referencesen | [10]V. Zvarych, M. Stasevych, V. Lunin, N.G. Deniz, C. Sayil, M. Ozyurek, K. Guclu, M. Vovk, V. Novikov, "Synthesis and investigation of antioxidant activity of the dithiocarbamate derivatives of 9,10-anthracenedione", Monatsh. Chem., vol. 147, pp. 2093-2101,2016. | |
| dc.relation.referencesen | [11]R. Apak, K. Güçlü, M. Özyürek, S.E. Karademir, "Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method," J. Agric. Food Chem., vol.52,pp.7970-7981, 2004. | |
| dc.relation.referencesen | [12]B. Bekdeşer, M. Özyürek, K. Güçlü, F. Üstün Alkan, R. Apak,"Development of a new catalase activity assay for biological samples using optical CUPRAC sensor," Spectrochim. Acta Part A, vol. 132, pp. 485-490, 2014. | |
| dc.citation.conference | 7th International youth science forum «Litteris et Artibus» | |
| dc.citation.journalTitle | Litteris et Artibus : матеріали | |
| dc.citation.spage | 32 | |
| dc.citation.epage | 33 | |
| dc.coverage.placename | Львів | |
| dc.coverage.placename | Lviv | |
| Appears in Collections: | Litteris et Artibus. – 2017 р.
|
