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  1. Електронний науковий архів Науково-технічної бібліотеки Національного університету "Львівська політехніка"
  2. Електронний архів Науково-технічної бібліотеки
  3. Вісники та науково-технічні збірники, журнали
  4. Chemistry & Chemical Technology
  5. Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1

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Please use this identifier to cite or link to this item: https://oldena.lpnu.ua/handle/ntb/43928
Title: Modification of alkyl esters of 4-aminobenzenethiosulfonic acid by S-triazine fragment and investigation of their growth-regulative activity
Other Titles: Модифікація алкілових естерів 4-амінобензентіосульфокислоти СИМ-триазиновим фрагментом та дослідження їх рістрегулювальної активності
Authors: Vasylyuk, Sofiya
Komarovska-Porokhnyavets, Olena
Novikov, Volodymyr
Lubenets, Vira
Affiliation: Lviv National Polytechnic University
Bibliographic description (Ukraine): 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.
Bibliographic description (International): 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.
Is part of: Chemistry & Chemical Technology, 1 (12), 2-18
Issue: 1
Volume: 12
Issue Date: 20-Jan-2018
Publisher: Lviv Politechnic Publishing House
Place of the edition/event: Lviv
Keywords: тіосульфокислотні похідні
тіосуль- фоестери
s-триазин
рістрегулювальна активність
thiosulfoacid derivatives
thiosulfoesters
s-triazine
growth-regulative activity
Number of pages: 5
Page range: 24-28
Start page: 24
End page: 28
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.
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.
URI: https://ena.lpnu.ua/handle/ntb/43928
Copyright owner: © Національний університет „Львівська політехніка“, 2018
© Vasylyuk S., Komarovska-Porokhnyavets O., Novikov V., Lubenets V., 2018
URL for reference material: https://doi.org/10.1016/j.ejmech.2005.10.013
https://doi.org/10.1002/jhet.890
https://doi.org/10.1016/j.bmcl.2006.07.052
https://doi.org/10.1002/hc.20631
https://doi.org/10.1016/S0031-9422(98)00015-6
https://doi.org/10.15407/biotech8.05.071
https://doi.org/10.1016/S0040-4039(01)01314-4
https://doi.org/10.1021/ja951134t
https://doi.org/10.1021/jo00048a007
https://doi.org/10.1002/ejoc.201700971
https://doi.org/10.1016/j.bbagen.2016.03.032
https://doi.org/10.1080/17415990412331317946
References (Ukraine): [1]Mykhaylichenko S., Chesnyuk A., Firhanh S. et al.: Pat. RU2230063, Publ. July 10, 2004.
[2] Kvak S., Tretyakova O., Kotlyarov N. et al.: Pat. RU 2091375, Publ. Sept. 27, 1997.
[3]Mel'nikov N.: Pestitsidy. Khimiya, Tekhnologiya i Primeneniye. Khimiya, Moskva 1987.
[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
[5] Polovkovych S., Karkhut A., Marintsova N. et al.: J. Heterocyclic Chem., 2013, 50, 1419.https://doi.org/10.1002/jhet.890
[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
[7] Kelarev V., Koshelev V., Belov N.: Khimiya Heterotsiklicheskikh Soyedineniy, 1994, 2, 240.
[8] Polovkovych S., Karkhut A., Marintsova N., Novikov V.: Heteroatom Chem., 2010, 21, 392. https://doi.org/10.1002/hc.20631
[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
[10] Lubenets V., Vasylyuk S., Baranovych D. et al.: Chem. Agric. Environ, 2007, 8, 163.
[11] Banya A., Karpenko O., Lubenets V. et al.: Biotechnologia Acta, 2015, 8, 71. https://doi.org/10.15407/biotech8.05.071
[12] Baranovych D., Lubenets V., Novikov V.: Ukr. Khim. Zh.,1999, 65, 130.
[13] Baranovych D., Komarovska O., Lubenets V., Novikov V.: Physiolohichno Aktyvni Rechovyny, 2000, 2, 33.
[14] Takada N., Watanabe N., Suenaga K. et al.: Tetrahedron Lett.,2001, 42, 6557. https://doi.org/10.1016/S0040-4039(01)01314-4
[15] Block E., Thiruvazhi M., Toscano P. et al.: J. Am. Chem. Soc.,1996, 118, 2790. https://doi.org/10.1021/ja951134t
[16] Block E., Shu-Hai Z.: J. Org. Chem., 1992, 57, 5815.https://doi.org/10.1021/jo00048a007
[17] Lubenets V.: Ukr. Khim. Zh., 2003, 69,109.
[18] Lubenets V., Vasylyuk S., Monka N. et al.: Pat. Ukr. 64412, Publ. Nov. 10, 2011.
[19] Halenova T., Nikolaeva I., Nakonechna A. et al.: Ukr. Biochem. J., 2015, 87, 83.
[20] Nawrot U., Zaczynska E., Czarny A. et al.:Mikologia Lekarska, 2012, 4, 143.
[21] Lubenets V., Karpenko O., PonomarenkoM. et al.: Chem. Chem. Technol., 2013, 7, 119.
[22] Shyam Pranab K., Soobin Son, Hye-Young Jang: Eur. J. Org. Chem., 2017, 34, 5025. https://doi.org/10.1002/ejoc.201700971
[23] SmithM., Hunter R., Stellenboom N. et al.: Biochim. Biophys. Acta, 2016, 1860, 1439.https://doi.org/10.1016/j.bbagen.2016.03.032.
[24] Lubenets V., Vasylyuk S., Baranovych D., Novikov V.: Pat. Ukr. 14985, Publ. Jun 15, 2006.
[25] Sergeyeva T.:Metodika Laboratornykh Ispytaniy Herbitsidov. Zashchita rasteniy, Moskva 1963.
[26] Bandgar B., Pandit S.: J. Sulfur Chem., 2004, 25, 347.https://doi.org/10.1080/17415990412331317946
[27] Vasylyuk S., Lubenets V., Bychko YU.I., Novykov V.P.: Khimiya geterotsiklicheskikh soyedineniy, 2008, 1, 132.
References (International): [1]Mykhaylichenko S., Chesnyuk A., Firhanh S. et al., Pat. RU2230063, Publ. July 10, 2004.
[2] Kvak S., Tretyakova O., Kotlyarov N. et al., Pat. RU 2091375, Publ. Sept. 27, 1997.
[3]Mel'nikov N., Pestitsidy. Khimiya, Tekhnologiya i Primeneniye. Khimiya, Moskva 1987.
[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
[5] Polovkovych S., Karkhut A., Marintsova N. et al., J. Heterocyclic Chem., 2013, 50, 1419.https://doi.org/10.1002/jhet.890
[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
[7] Kelarev V., Koshelev V., Belov N., Khimiya Heterotsiklicheskikh Soyedineniy, 1994, 2, 240.
[8] Polovkovych S., Karkhut A., Marintsova N., Novikov V., Heteroatom Chem., 2010, 21, 392. https://doi.org/10.1002/hc.20631
[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
[10] Lubenets V., Vasylyuk S., Baranovych D. et al., Chem. Agric. Environ, 2007, 8, 163.
[11] Banya A., Karpenko O., Lubenets V. et al., Biotechnologia Acta, 2015, 8, 71. https://doi.org/10.15407/biotech8.05.071
[12] Baranovych D., Lubenets V., Novikov V., Ukr. Khim. Zh.,1999, 65, 130.
[13] Baranovych D., Komarovska O., Lubenets V., Novikov V., Physiolohichno Aktyvni Rechovyny, 2000, 2, 33.
[14] Takada N., Watanabe N., Suenaga K. et al., Tetrahedron Lett.,2001, 42, 6557. https://doi.org/10.1016/S0040-4039(01)01314-4
[15] Block E., Thiruvazhi M., Toscano P. et al., J. Am. Chem. Soc.,1996, 118, 2790. https://doi.org/10.1021/ja951134t
[16] Block E., Shu-Hai Z., J. Org. Chem., 1992, 57, 5815.https://doi.org/10.1021/jo00048a007
[17] Lubenets V., Ukr. Khim. Zh., 2003, 69,109.
[18] Lubenets V., Vasylyuk S., Monka N. et al., Pat. Ukr. 64412, Publ. Nov. 10, 2011.
[19] Halenova T., Nikolaeva I., Nakonechna A. et al., Ukr. Biochem. J., 2015, 87, 83.
[20] Nawrot U., Zaczynska E., Czarny A. et al.:Mikologia Lekarska, 2012, 4, 143.
[21] Lubenets V., Karpenko O., PonomarenkoM. et al., Chem. Chem. Technol., 2013, 7, 119.
[22] Shyam Pranab K., Soobin Son, Hye-Young Jang: Eur. J. Org. Chem., 2017, 34, 5025. https://doi.org/10.1002/ejoc.201700971
[23] SmithM., Hunter R., Stellenboom N. et al., Biochim. Biophys. Acta, 2016, 1860, 1439.https://doi.org/10.1016/j.bbagen.2016.03.032.
[24] Lubenets V., Vasylyuk S., Baranovych D., Novikov V., Pat. Ukr. 14985, Publ. Jun 15, 2006.
[25] Sergeyeva T.:Metodika Laboratornykh Ispytaniy Herbitsidov. Zashchita rasteniy, Moskva 1963.
[26] Bandgar B., Pandit S., J. Sulfur Chem., 2004, 25, 347.https://doi.org/10.1080/17415990412331317946
[27] Vasylyuk S., Lubenets V., Bychko YU.I., Novykov V.P., Khimiya geterotsiklicheskikh soyedineniy, 2008, 1, 132.
Content type: Article
Appears in Collections:Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 1

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