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Îëåíà Êîâòóí
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Ñó÷àñíà òåðì³íîëîã³ÿ òà íîìåíêëàòóðà îðãàí³÷íèõ ñïîëóê: Íàâ÷àëüíîìåòîäè÷íèé ïîñ³áíèê äëÿ â÷èòåë³â òà ó÷í³â çàãàëüíîîñâ³òí³õ íàâ÷àëüíèõ çàêëàä³â
ÂÑ Òîëìà÷îâà, ÎÌ Êîâòóí, ÌÞ Êîðí³ëîâ, ΠÃîð䳺íêî, Ñ Âàñèëåíêî
Òåðíîï³ëü: Íàâ÷àëüíà êíèãà–Áîãäàí, 2008
142008
PMR SPECTRA AND CONFORMATIONS OF BENZODIOXANE AND BENZODIOXEPANE DERIVATIVES OF FLAVANONE AND ISOFLAVANONE
VP Khilya, D Litkei, EN Kovtun, KA BUDI, MY Kornilov, AV Turov
ZHURNAL ORGANICHESKOI KHIMII 27 (4), 690-700, 1991
71991
Íîìåíêëàòóðà îðãàí³÷íèõ ñïîëóê. Íàâ÷àëüíèé ïîñ³áíèê
ÂÑ Òîëìà÷îâà, ÎÌ Êîâòóí, ÎÀ Äóáîâèê, ÑÑ Ô³öàéëî
Òåðíîï³ëü:«Ìàíäð³âåöü, 2011
52011
Chemistry of Isoflavone Heteroanalogs. Part 10. Synthesis of Pyrimidines by Recyclization of Isoflavones and Their Heteroanalogs.
VP Khilya, MY Kornilov, NV Gorbulenko, GM Golubushina, EN Kovtun, ...
Chemischer Informationsdienst 17 (15), no-no, 1986
51986
Chemistry of isoflavone heterocyclic analogs. 10. Synthesis of pyrimidines by recyclization of isoflavones and their heterocyclic analogs
VP Khilya, MY Kornilov, NV Gorbulenko, GM Golubushina, EN Kovtun, ...
Chemistry of Heterocyclic Compounds 21, 1273-1279, 1985
31985
Íîìåíêëàòóðí³ ñèñòåìè â êîíòåêñò³ ðîçâèòêó òåîðåòè÷íèõ óÿâëåíü â îðãàí³÷í³é õ³ì³¿
Î Êîâòóí,  Òîëìà÷îâà, Ì Êîðí³ëîâ, Î Ãîð䳺íêî, Ñ ²ñàºâ
Âèäàâíèöòâî Ëüâ³âñüêî¿ ïîë³òåõí³êè, 2012
22012
ÑÓ×ÀÑÍÀ ղ̲×ÍÀ ÒÅÐ̲ÍÎËÎÃ²ß ÒÀ ÍÎÌÅÍÊËÀÒÓÐÀ ÎÐÃÀͲ×Íί ղ̲¯
Î Ãîð䳺íêî, Ì Êîðí³ëîâ, Î Ãîëóá, Ñ ²ñàºâ,  Òîëìà÷îâà, Î Êîâòóí
Ãîð䳺íêî, Ì. Êîðí³ëîâ, Î. Ãîëóá, Ñ. ²ñàºâ, Â. Òîëìà÷îâà, Î. Êîâòóí//³ñí …, 2008
12008
ÄÎÑ˲ÄÍÎ-ÅÊÑÏÅÐÅÌÅÍÒÀËÜÍÀ ÏÅÐŲÐÊÀ ÅÔÅÊÒÈÂÍÎÑÒ² ÏÅÄÀÃÎò×ÍÈÕ ÓÌΠÔÎÐÌÓÂÀÍÍß Ñ²ÒÎÃËßÄÍί ÊÓËÜÒÓÐÈ ÌÀÉÁÓÒÍ²Õ ÌÅÄÈ×ÍÈÕ ÑÅÑÒÅÐ ÍÀ ÎÑÍβ ÐÅÀ˲ÇÀÖ²¯ ÄÅÎÍÒÎËÎò×ÍÎÃΠϲÄÕÎÄÓ
ÎÌ Êîâòóí
Íàóêîâ³ äîñÿãíåííÿ, â³äêðèòòÿ òà øëÿõè ðîçâèòêó ïåäàãîã³÷íî¿ íàóêè, 24-25, 0
1
ÏÐÎÁËÅÌÈ ÒÐÀÍÑÔÎÐÌÀÖ²¯ ղ̲×ÍÈÕ ÒÅÐ̲ͲÂ
ÌÞ Êîðí³ëîâ, ÎÀ Ãîëóá, ΠÃîð䳺íêî, ÂÑ Òîëìà÷îâà, ÎÌ Êîâòóí
1
²ÌÅͲ ÌÏ ÄÐÀÃÎÌÀÍÎÂÀ
ÂÀ Áîãàòèðåíêî, À Êðàâ÷åíêî, ÂÌ Ëàâð³íåíêî, ÒÀ Ãðèíþê, ...
Ìàðêåòèíã 9, 30, 2020
2020
³ëüí³ ðàäèêàëè â õ³ì³¿ BODIPY
ÂÏ ²âàíñüêèé, ÎÌ Êîâòóí
Ðåäàêö³éíà ðàäà, 18, 2017
2017
Áóäîâà òà âëàñòèâîñò³ ìåòàëîâì³ñíèõ â³òàì³í³â
ÎÌ Êîâòóí
Ðåäàêö³éíà ðàäà, 3, 2016
2016
Äîñë³äæåííÿ ë³êàðñüêèõ çàñîá³â íà îñíîâ³ îêñîïîõ³äíèõ âóãëåâîäí³â
ÎÌ Êîâòóí
Ðåäàêö³éíà ðàäà, 41, 2016
2016
Ã˲ÊÎÀËÊÀËίÄÈ SOLANUM TUBEROSUM
ÎÌ Êîâòóí, ÌÂ Ìàêàð÷óê
ÐÎÇÄ²Ë ². ÔÓÍÄÀÌÅÍÒÀËÜÍÀ ϲÄÃÎÒÎÂÊÀ ÌÀÉÁÓÒÍÜÎÃÎ Â×ÈÒÅËß Õ²Ì²¯ ÒÀ ØËßÕÈ ¯¯ …, 2015
2015
ÌÅÒÎÄ ÒÅÑÒÓÂÀÍÍß Â ÊÓÐѲ «²ÑÒÎÐ²ß Õ²Ì²¯» ÄËß ÌÀÉÁÓÒÍ²Õ Ó×ÈÒÅ˲Â
ÎÌ Êîâòóí, ÎÑ Ïàíàñþê
ÐÎÇÄ²Ë ². ÔÓÍÄÀÌÅÍÒÀËÜÍÀ ϲÄÃÎÒÎÂÊÀ ÌÀÉÁÓÒÍÜÎÃÎ Â×ÈÒÅËß Õ²Ì²¯ ÒÀ ØËßÕÈ ¯¯ …, 2015
2015
ϲÄÂÈÙÅÍÍß ÅÔÅÊÒÈÂÍÎÑÒ² ÔÎÐÌÓÂÀÍÍß ÇÍÀÍÜ Ç Á²ÎÎÐÃÀͲ×Íί ղ̲¯ ÍÀ ÎÑÍβ ÏÐÈÍÖÈÏÓ Â²ÇÓÀ˲ÇÀÖ²¯
ÎÌ Êîâòóí, ÕÀ Ãîðîõ³âñüêà
ÐÎÇÄ²Ë ². ÔÓÍÄÀÌÅÍÒÀËÜÍÀ ϲÄÃÎÒÎÂÊÀ ÌÀÉÁÓÒÍÜÎÃÎ Â×ÈÒÅËß Õ²Ì²¯ ÒÀ ØËßÕÈ ¯¯ …, 2015
2015
ÁÎÐÎÄÈϲÐÎÌÅÒÅÍÎÖ²ÀͲÍÈ ÍÀ ÎÑÍβ ÄÈÕËÎÐÎÇÀ̲ÙÅÍÎÃÎ BODIPY
ÒÎ Ãí³äåíêî, ÂÏ ßêóáîâñüêèé, ÎÌ Êîâòóí
È ÏÐÈÊËÀÄÍÛÅ ÈÑÑËÅÄÎÂÀÍÈß Â ÑÎÂÐÅÌÅÍÍÎÉ ÕÈÌÈÈ, 32, 2014
2014
ÎÑÍÎÂͲ ÏÐÈÍÖÈÏÈ ÍÎÌÅÍÊËÀÒÓÐÈ IUPAC  ÎÐÃÀͲ×Í²É Õ²Ì²¯
ÎÌ Êîâòóí, ÂÑ Òîëìà÷îâà
ÍÀÓÊβ ÇÀÏÈÑÊÈ, 253, 2008
2008
PMR SPECTRA AND CONFORMATIONS OF BENZODIOXANE AND BENZODIOXEPAN DERIVATIVES OF FLAVANONE AND ISOFLAVANONE
VP KHILYA, D LITKEI, EN KOVTUN, K AL'BUDI, Y KORNILOV, ...
Journal of organic chemistry of the USSR 27 (4), 595-603, 1991
1991
ÔÎÐÌÓÂÀÍÍß ÊÐÈÒÈ×ÍÎÃÎ ÌÈÑËÅÍÍß Ó ÑÒÀÐØÎÊËÀÑÍÈÊ²Â Ï²Ä ×ÀÑ ÂÈÂ×ÅÍÍß ÍÎÂÅË ÍÀ ÓÐÎÊÀÕ ÓÊÐÀ¯ÍÑÜÊί ˲ÒÅÐÀÒÓÐÈ
Î Êîâòóí
Ðåêîìåíäîâàíî äî äðóêó ð³øåííÿì â÷åíî¿ ðàäè Ãëóõ³âñüêîãî íàö³îíàëüíîãî …, 0
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