DC Field | Value | Language |
dc.contributor.author | Vasylyuk, Sofiya | |
dc.contributor.author | Komarovska-Porokhnyavets, Olena | |
dc.contributor.author | Novikov, Volodymyr | |
dc.contributor.author | Lubenets, Vira | |
dc.date.accessioned | 2019-01-29T12:53:43Z | - |
dc.date.available | 2019-01-29T12:53:43Z | - |
dc.date.created | 2018-01-20 | |
dc.date.issued | 2018-01-20 | |
dc.identifier.citation | Modification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity / Sofiya Vasylyuk, Olena Komarovska-Porokhnyavets, Volodymyr Novikov, Vira Lubenets // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 24–28. | |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/43928 | - |
dc.description.abstract | Досліджено ацилювання аміногрупи алкі-
лових S-естерів 4-амінобензентіосульфокислоти ціанурхло-
ридом. Серію естерів із триазиновим фрагментом було
синтезовано та охарактеризовано елементарним аналізом, 1H-
ЯМР та ІЧ-спектроскопією. Досліджено рістрегулювальну ак-
тивність синтезованих сполук. Визначено певний вплив струк-
тури тіосульфоестерів на їх рістрегулювальну активність. | |
dc.description.abstract | The acylation of aminogroup of alkyl S-esters
4-aminobenzenthiosulfoacid with cyanurchloride was
investigated. Series of esters with triazine fragment were
synthesized and characterized by elemental analysis,
1H NMR and IR spectroscopy. The growth-regulative
activity of the synthesized compounds was researched.
Some appropriate effect of thiosulfoesters structure upon
their growth-regulative activity was determined. | |
dc.format.extent | 24-28 | |
dc.language.iso | en | |
dc.publisher | Lviv Politechnic Publishing House | |
dc.relation.ispartof | Chemistry & Chemical Technology, 1 (12), 2-18 | |
dc.relation.uri | https://doi.org/10.1016/j.ejmech.2005.10.013 | |
dc.relation.uri | https://doi.org/10.1002/jhet.890 | |
dc.relation.uri | https://doi.org/10.1016/j.bmcl.2006.07.052 | |
dc.relation.uri | https://doi.org/10.1002/hc.20631 | |
dc.relation.uri | https://doi.org/10.1016/S0031-9422(98)00015-6 | |
dc.relation.uri | https://doi.org/10.15407/biotech8.05.071 | |
dc.relation.uri | https://doi.org/10.1016/S0040-4039(01)01314-4 | |
dc.relation.uri | https://doi.org/10.1021/ja951134t | |
dc.relation.uri | https://doi.org/10.1021/jo00048a007 | |
dc.relation.uri | https://doi.org/10.1002/ejoc.201700971 | |
dc.relation.uri | https://doi.org/10.1016/j.bbagen.2016.03.032 | |
dc.relation.uri | https://doi.org/10.1080/17415990412331317946 | |
dc.subject | тіосульфокислотні похідні | |
dc.subject | тіосуль- фоестери | |
dc.subject | s-триазин | |
dc.subject | рістрегулювальна активність | |
dc.subject | thiosulfoacid derivatives | |
dc.subject | thiosulfoesters | |
dc.subject | s-triazine | |
dc.subject | growth-regulative activity | |
dc.title | Modification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity | |
dc.title.alternative | Модифікація алкілових естерів 4-амінобензентіосульфокислоти СИМ-триазиновим фрагментом та дослідження їх рістрегулювальної активності | |
dc.type | Article | |
dc.rights.holder | © Національний університет „Львівська політехніка“, 2018 | |
dc.rights.holder | © Vasylyuk S., Komarovska-Porokhnyavets O., Novikov V.,
Lubenets V., 2018 | |
dc.contributor.affiliation | Lviv National Polytechnic University | |
dc.format.pages | 5 | |
dc.identifier.citationen | Modification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity / Sofiya Vasylyuk, Olena Komarovska-Porokhnyavets, Volodymyr Novikov, Vira Lubenets // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2-18. — Vol 12. — No 1. — P. 24–28. | |
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dc.relation.references | [14] Takada N., Watanabe N., Suenaga K. et al.: Tetrahedron Lett.,2001, 42, 6557. https://doi.org/10.1016/S0040-4039(01)01314-4 | |
dc.relation.references | [15] Block E., Thiruvazhi M., Toscano P. et al.: J. Am. Chem. Soc.,1996, 118, 2790. https://doi.org/10.1021/ja951134t | |
dc.relation.references | [16] Block E., Shu-Hai Z.: J. Org. Chem., 1992, 57, 5815.https://doi.org/10.1021/jo00048a007 | |
dc.relation.references | [17] Lubenets V.: Ukr. Khim. Zh., 2003, 69,109. | |
dc.relation.references | [18] Lubenets V., Vasylyuk S., Monka N. et al.: Pat. Ukr. 64412, Publ. Nov. 10, 2011. | |
dc.relation.references | [19] Halenova T., Nikolaeva I., Nakonechna A. et al.: Ukr. Biochem. J., 2015, 87, 83. | |
dc.relation.references | [20] Nawrot U., Zaczynska E., Czarny A. et al.:Mikologia Lekarska, 2012, 4, 143. | |
dc.relation.references | [21] Lubenets V., Karpenko O., PonomarenkoM. et al.: Chem. Chem. Technol., 2013, 7, 119. | |
dc.relation.references | [22] Shyam Pranab K., Soobin Son, Hye-Young Jang: Eur. J. Org. Chem., 2017, 34, 5025. https://doi.org/10.1002/ejoc.201700971 | |
dc.relation.references | [23] SmithM., Hunter R., Stellenboom N. et al.: Biochim. Biophys. Acta, 2016, 1860, 1439.https://doi.org/10.1016/j.bbagen.2016.03.032. | |
dc.relation.references | [24] Lubenets V., Vasylyuk S., Baranovych D., Novikov V.: Pat. Ukr. 14985, Publ. Jun 15, 2006. | |
dc.relation.references | [25] Sergeyeva T.:Metodika Laboratornykh Ispytaniy Herbitsidov. Zashchita rasteniy, Moskva 1963. | |
dc.relation.references | [26] Bandgar B., Pandit S.: J. Sulfur Chem., 2004, 25, 347.https://doi.org/10.1080/17415990412331317946 | |
dc.relation.references | [27] Vasylyuk S., Lubenets V., Bychko YU.I., Novykov V.P.: Khimiya geterotsiklicheskikh soyedineniy, 2008, 1, 132. | |
dc.relation.referencesen | [1]Mykhaylichenko S., Chesnyuk A., Firhanh S. et al., Pat. RU2230063, Publ. July 10, 2004. | |
dc.relation.referencesen | [2] Kvak S., Tretyakova O., Kotlyarov N. et al., Pat. RU 2091375, Publ. Sept. 27, 1997. | |
dc.relation.referencesen | [3]Mel'nikov N., Pestitsidy. Khimiya, Tekhnologiya i Primeneniye. Khimiya, Moskva 1987. | |
dc.relation.referencesen | [4] Saczewski F., Bulakowska A., Bednarski P., Grunert R., Eur. J. Med. Chem., 2006, 41, 219.https://doi.org/10.1016/j.ejmech.2005.10.013 | |
dc.relation.referencesen | [5] Polovkovych S., Karkhut A., Marintsova N. et al., J. Heterocyclic Chem., 2013, 50, 1419.https://doi.org/10.1002/jhet.890 | |
dc.relation.referencesen | [6] Zhou Y., Sun Z., Froelich J. M., Hermann T., Wall D., Bioorg. Med. Chem. Lett., 2006, 16, 5451.https://doi.org/10.1016/j.bmcl.2006.07.052 | |
dc.relation.referencesen | [7] Kelarev V., Koshelev V., Belov N., Khimiya Heterotsiklicheskikh Soyedineniy, 1994, 2, 240. | |
dc.relation.referencesen | [8] Polovkovych S., Karkhut A., Marintsova N., Novikov V., Heteroatom Chem., 2010, 21, 392. https://doi.org/10.1002/hc.20631 | |
dc.relation.referencesen | [9] Su J.-Y., Xu X.-H., Zeng L.-M. et al., Phytochemistry, 1998, 48,583. https://doi.org/10.1016/S0031-9422(98)00015-6 | |
dc.relation.referencesen | [10] Lubenets V., Vasylyuk S., Baranovych D. et al., Chem. Agric. Environ, 2007, 8, 163. | |
dc.relation.referencesen | [11] Banya A., Karpenko O., Lubenets V. et al., Biotechnologia Acta, 2015, 8, 71. https://doi.org/10.15407/biotech8.05.071 | |
dc.relation.referencesen | [12] Baranovych D., Lubenets V., Novikov V., Ukr. Khim. Zh.,1999, 65, 130. | |
dc.relation.referencesen | [13] Baranovych D., Komarovska O., Lubenets V., Novikov V., Physiolohichno Aktyvni Rechovyny, 2000, 2, 33. | |
dc.relation.referencesen | [14] Takada N., Watanabe N., Suenaga K. et al., Tetrahedron Lett.,2001, 42, 6557. https://doi.org/10.1016/S0040-4039(01)01314-4 | |
dc.relation.referencesen | [15] Block E., Thiruvazhi M., Toscano P. et al., J. Am. Chem. Soc.,1996, 118, 2790. https://doi.org/10.1021/ja951134t | |
dc.relation.referencesen | [16] Block E., Shu-Hai Z., J. Org. Chem., 1992, 57, 5815.https://doi.org/10.1021/jo00048a007 | |
dc.relation.referencesen | [17] Lubenets V., Ukr. Khim. Zh., 2003, 69,109. | |
dc.relation.referencesen | [18] Lubenets V., Vasylyuk S., Monka N. et al., Pat. Ukr. 64412, Publ. Nov. 10, 2011. | |
dc.relation.referencesen | [19] Halenova T., Nikolaeva I., Nakonechna A. et al., Ukr. Biochem. J., 2015, 87, 83. | |
dc.relation.referencesen | [20] Nawrot U., Zaczynska E., Czarny A. et al.:Mikologia Lekarska, 2012, 4, 143. | |
dc.relation.referencesen | [21] Lubenets V., Karpenko O., PonomarenkoM. et al., Chem. Chem. Technol., 2013, 7, 119. | |
dc.relation.referencesen | [22] Shyam Pranab K., Soobin Son, Hye-Young Jang: Eur. J. Org. Chem., 2017, 34, 5025. https://doi.org/10.1002/ejoc.201700971 | |
dc.relation.referencesen | [23] SmithM., Hunter R., Stellenboom N. et al., Biochim. Biophys. Acta, 2016, 1860, 1439.https://doi.org/10.1016/j.bbagen.2016.03.032. | |
dc.relation.referencesen | [24] Lubenets V., Vasylyuk S., Baranovych D., Novikov V., Pat. Ukr. 14985, Publ. Jun 15, 2006. | |
dc.relation.referencesen | [25] Sergeyeva T.:Metodika Laboratornykh Ispytaniy Herbitsidov. Zashchita rasteniy, Moskva 1963. | |
dc.relation.referencesen | [26] Bandgar B., Pandit S., J. Sulfur Chem., 2004, 25, 347.https://doi.org/10.1080/17415990412331317946 | |
dc.relation.referencesen | [27] Vasylyuk S., Lubenets V., Bychko YU.I., Novykov V.P., Khimiya geterotsiklicheskikh soyedineniy, 2008, 1, 132. | |
dc.citation.volume | 12 | |
dc.citation.issue | 1 | |
dc.citation.spage | 24 | |
dc.citation.epage | 28 | |
dc.coverage.placename | Lviv | |
Appears in Collections: | Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1
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