Synthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives

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dc.citation.epage428
dc.citation.issue4
dc.citation.spage424
dc.contributor.affiliationOles Honchar Dnipro National University
dc.contributor.affiliationDnipro State Agrarian and Economic University
dc.contributor.authorPalchykov, Vitalii
dc.contributor.authorKhromykh, Nina
dc.contributor.authorLykholat, Yurii
dc.contributor.authorMykolenko, Svitlana
dc.contributor.authorLykholat, Tetyana
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
dc.date.accessioned2020-03-03T09:04:22Z
dc.date.available2020-03-03T09:04:22Z
dc.date.created2019-02-28
dc.date.issued2019-02-28
dc.description.abstractСинтезовано 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.
dc.description.abstractA 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.
dc.format.extent424-428
dc.format.pages5
dc.identifier.citationSynthesis 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.
dc.identifier.citationenSynthesis 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.
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/46510
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 4 (13), 2019
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dc.relation.referencesen1. Palchykov V., Vestnik Dnipropetrovsk Univ., 2010, 18, 63.
dc.relation.referencesen2. Brant M., Wulff J., Synthesis, 2016, 48, 1. https://doi.org/10.1055/s-0035-1560351
dc.relation.referencesen3. Pallaoro D., Avelino A., Camili E. et al., J. Seed Sci., 2016, 38, 227. https://doi.org/10.1590/2317-1545v38n3163847
dc.relation.referencesen4. Fawcett J., Koopman Z., Miller L., Farm Prog. Rep., 2016, 2015, paper 152. https://doi.org/10.31274/farmprogressreports-180814-1390
dc.relation.referencesen5. Palchykov V., Zarovnaya I., Tretiakov S. et al., J. Mol. Struct., 2018, 1157, 149. https://doi.org/10.1016/j.molstruc.2017.12.055
dc.relation.referencesen6. Zarovnaya I., Zlenko H., Palchikov V., Eur. Chem. Bull., 2014, 3, 543. https://doi.org/10.17628/ecb.2014.3.543-547
dc.relation.referencesen7. Kas’yan L., Prid’ma S., Turov A. et al., Russ. J. Org. Chem., 2009, 45, 505. https://doi.org/10.1134/S107042800904006X
dc.relation.referencesen8. Chou T.-S., Tso H.-H., Chang L.-J., J. Chem. Soc., Perkin Trans. 1, 1985, 515. https://doi.org/10.1039/P19850000515
dc.relation.referencesen9. Dezfuli P., Sharif-Zadeh F., Janmohammadi M., ARPN J. Agricult. Biol. Sci., 2008, 3, 22.
dc.relation.referencesen10. Lagunin A., Zakharov A., Filimonov D., Poroikov V.:Mol. Inform., 2011, 30, 241. https://doi.org/10.1002/minf.201000151
dc.relation.referencesen11. Schluttenhofer C., Ross J., Mason T. et al., PurdueMethods for Corn Growth, 2010, paper 11.
dc.relation.referencesen12. Khromykh N., Shupranova L., Lykholat Y. et al., Visnyk Dnipropetrovsk Univ., 2015, 23, 100. https://doi.org/10.15421/011514
dc.relation.referencesen13. Shcherbyna R., Danilchenko D., Parchenko V. et al., Res. J. Pharm., Biol. Chem. Sci., 2017, 8, 975.
dc.relation.urihttps://doi.org/10.1055/s-0035-1560351
dc.relation.urihttps://doi.org/10.1590/2317-1545v38n3163847
dc.relation.urihttps://doi.org/10.31274/farmprogressreports-180814-1390
dc.relation.urihttps://doi.org/10.1016/j.molstruc.2017.12.055
dc.relation.urihttps://doi.org/10.17628/ecb.2014.3.543-547
dc.relation.urihttps://doi.org/10.1134/S107042800904006X
dc.relation.urihttps://doi.org/10.1039/P19850000515
dc.relation.urihttps://doi.org/10.1002/minf.201000151
dc.relation.urihttps://doi.org/10.15421/011514
dc.rights.holder© Національний університет „Львівська політехніка“, 2019
dc.rights.holder© Palchykov V., Khromykh N., Lykholat Yu., Mykolenko S., 2019
dc.subjectсульфолани
dc.subjectрістрегулююча активність
dc.subjectZea mays
dc.subjectпроростки
dc.subjectіндекс проростання
dc.subjectsulfolanes
dc.subjectplant growth regulatory activity
dc.subjectZea mays
dc.subjectseedlings
dc.subjectvigor index
dc.titleSynthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives
dc.title.alternativeСинтез та рістрегулююча активність похідних 3-сульфолену
dc.typeArticle

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Chemistry & Chemical Technology. – 2019. – Vol. 13, No. 4