https://oldena.lpnu.ua/handle/ntb/46510
Title: | Synthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives |
Other Titles: | Синтез та рістрегулююча активність похідних 3-сульфолену |
Authors: | Palchykov, Vitalii Khromykh, Nina Lykholat, Yurii Mykolenko, Svitlana Lykholat, Tetyana |
Affiliation: | Oles Honchar Dnipro National University Dnipro State Agrarian and Economic University |
Bibliographic description (Ukraine): | Synthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives / Vitalii Palchykov, Nina Khromykh, Yurii Lykholat, Svitlana Mykolenko, Tetyana Lykholat // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 4. — P. 424–428. |
Bibliographic description (International): | Synthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives / Vitalii Palchykov, Nina Khromykh, Yurii Lykholat, Svitlana Mykolenko, Tetyana Lykholat // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 4. — P. 424–428. |
Is part of: | Chemistry & Chemical Technology, 4 (13), 2019 |
Issue: | 4 |
Issue Date: | 28-Feb-2019 |
Publisher: | Видавництво Львівської політехніки Lviv Politechnic Publishing House |
Place of the edition/event: | Львів Lviv |
Keywords: | сульфолани рістрегулююча активність Zea mays проростки індекс проростання sulfolanes plant growth regulatory activity Zea mays seedlings vigor index |
Number of pages: | 5 |
Page range: | 424-428 |
Start page: | 424 |
End page: | 428 |
Abstract: | Синтезовано ряд циклічних сульфонових похідних з 3-сульфолену, які були протестовані на рістрегулюючу
активність на проростках кукурудзи Zea mays. Показано, що
збільшення індексу проростання, а також довжини кореня і
стебла досягалось завдяки обробленню 3-сульфоленом, 3-аміно-4-морфолінотетрагідротіофен-1,1-діоксидом та цис-4-((2,4-дихлорфеніл)аміно)-3-гідрокситетрагідротіофен-1,1-діоксидом. A small series of cyclic sulfone derivatives were synthesized starting from readily available 3-sulfolene. All compounds were tested for plant growth regulatory activity on the maize seedlings Zea mays. Obtained results showed the greatest increase in vigor index, root and shoot length due to the treatment with the 3-sulfolene, 3-amino-4-morpholinotetrahydrothiophene 1,1-dioxide and cis-4-((2,4-dichlorophenyl)amino)-3-hydroxytetrahydrothiophene 1,1-dioxide. |
URI: | https://ena.lpnu.ua/handle/ntb/46510 |
Copyright owner: | © Національний університет „Львівська політехніка“, 2019 © Palchykov V., Khromykh N., Lykholat Yu., Mykolenko S., 2019 |
URL for reference material: | https://doi.org/10.1055/s-0035-1560351 https://doi.org/10.1590/2317-1545v38n3163847 https://doi.org/10.31274/farmprogressreports-180814-1390 https://doi.org/10.1016/j.molstruc.2017.12.055 https://doi.org/10.17628/ecb.2014.3.543-547 https://doi.org/10.1134/S107042800904006X https://doi.org/10.1039/P19850000515 https://doi.org/10.1002/minf.201000151 https://doi.org/10.15421/011514 |
References (Ukraine): | 1. Palchykov V.: Vestnik Dnipropetrovsk Univ., 2010, 18, 63. 2. Brant M., Wulff J.: Synthesis, 2016, 48, 1. https://doi.org/10.1055/s-0035-1560351 3. Pallaoro D., Avelino A., Camili E. et al.: J. Seed Sci., 2016, 38, 227. https://doi.org/10.1590/2317-1545v38n3163847 4. Fawcett J., Koopman Z., Miller L.: Farm Prog. Rep., 2016, 2015, paper 152. https://doi.org/10.31274/farmprogressreports-180814-1390 5. Palchykov V., Zarovnaya I., Tretiakov S. et al.: J. Mol. Struct., 2018, 1157, 149. https://doi.org/10.1016/j.molstruc.2017.12.055 6. Zarovnaya I., Zlenko H., Palchikov V.: Eur. Chem. Bull., 2014, 3, 543. https://doi.org/10.17628/ecb.2014.3.543-547 7. Kas’yan L., Prid’ma S., Turov A. et al.: Russ. J. Org. Chem., 2009, 45, 505. https://doi.org/10.1134/S107042800904006X 8. Chou T.-S., Tso H.-H., Chang L.-J.: J. Chem. Soc., Perkin Trans. 1, 1985, 515. https://doi.org/10.1039/P19850000515 9. Dezfuli P., Sharif-Zadeh F., Janmohammadi M.: ARPN J. Agricult. Biol. Sci., 2008, 3, 22. 10. Lagunin A., Zakharov A., Filimonov D., Poroikov V.:Mol. Inform., 2011, 30, 241. https://doi.org/10.1002/minf.201000151 11. Schluttenhofer C., Ross J., Mason T. et al.: PurdueMethods for Corn Growth, 2010, paper 11. 12. Khromykh N., Shupranova L., Lykholat Y. et al.: Visnyk Dnipropetrovsk Univ., 2015, 23, 100. https://doi.org/10.15421/011514 13. Shcherbyna R., Danilchenko D., Parchenko V. et al.: Res. J. Pharm., Biol. Chem. Sci., 2017, 8, 975. |
References (International): | 1. Palchykov V., Vestnik Dnipropetrovsk Univ., 2010, 18, 63. 2. Brant M., Wulff J., Synthesis, 2016, 48, 1. https://doi.org/10.1055/s-0035-1560351 3. Pallaoro D., Avelino A., Camili E. et al., J. Seed Sci., 2016, 38, 227. https://doi.org/10.1590/2317-1545v38n3163847 4. Fawcett J., Koopman Z., Miller L., Farm Prog. Rep., 2016, 2015, paper 152. https://doi.org/10.31274/farmprogressreports-180814-1390 5. Palchykov V., Zarovnaya I., Tretiakov S. et al., J. Mol. Struct., 2018, 1157, 149. https://doi.org/10.1016/j.molstruc.2017.12.055 6. Zarovnaya I., Zlenko H., Palchikov V., Eur. Chem. Bull., 2014, 3, 543. https://doi.org/10.17628/ecb.2014.3.543-547 7. Kas’yan L., Prid’ma S., Turov A. et al., Russ. J. Org. Chem., 2009, 45, 505. https://doi.org/10.1134/S107042800904006X 8. Chou T.-S., Tso H.-H., Chang L.-J., J. Chem. Soc., Perkin Trans. 1, 1985, 515. https://doi.org/10.1039/P19850000515 9. Dezfuli P., Sharif-Zadeh F., Janmohammadi M., ARPN J. Agricult. Biol. Sci., 2008, 3, 22. 10. Lagunin A., Zakharov A., Filimonov D., Poroikov V.:Mol. Inform., 2011, 30, 241. https://doi.org/10.1002/minf.201000151 11. Schluttenhofer C., Ross J., Mason T. et al., PurdueMethods for Corn Growth, 2010, paper 11. 12. Khromykh N., Shupranova L., Lykholat Y. et al., Visnyk Dnipropetrovsk Univ., 2015, 23, 100. https://doi.org/10.15421/011514 13. Shcherbyna R., Danilchenko D., Parchenko V. et al., Res. J. Pharm., Biol. Chem. Sci., 2017, 8, 975. |
Content type: | Article |
Appears in Collections: | Chemistry & Chemical Technology. – 2019. – Vol. 13, No. 4 |
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