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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. – 2019. – Vol. 13, No. 2

putin IS MURDERER

Please use this identifier to cite or link to this item: https://oldena.lpnu.ua/handle/ntb/46469
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dc.contributor.authorKovaleva, Svitlana
dc.contributor.authorMayboroda, Olena
dc.contributor.authorSimurova, Natalia
dc.contributor.authorMazur, Larysa
dc.date.accessioned2020-03-02T12:28:12Z-
dc.date.available2020-03-02T12:28:12Z-
dc.date.created2019-02-28
dc.date.issued2019-02-28
dc.identifier.citationSynthesis of Annelated P- and N-containing Heterocycles Based on Methyl 5-Aminothiophene-2-Carboxylate Derivatives / Svitlana Kovaleva, Olena Mayboroda, Natalia Simurova, Larysa Mazur // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 2. — P. 145–149.
dc.identifier.urihttps://ena.lpnu.ua/handle/ntb/46469-
dc.description.abstractСинтезовані похідні нових біциклічних систем – 1H-тієно[3,2-c][1,5,2]оксазофосфініну і 1,2-дігідро- тієно[2,3-b][1,4] азафосфініну за реакцією фосфорилювання N- заміщених похідних 2-аміно-5-метоксикарбонілтіофену з трибромідом фосфору(III). Показано, що гетероциклізація може бути проведена в основному середовищі і за м'яких умов. Методами хімічного аналізу, 1H і 31P ЯМР спектроскопії вивчено кінцеві продукти реакції.
dc.description.abstractDerivatives of new bicyclic systems – 1H-thieno[3,2-c][1,5,2]oxazaphosphinine and 1,2-dihydrothieno[ 2,3-b][1,4]azaphosphinine have been obtained by phosphorylation of N-substituted derivatives of 5-amino- 2-methoxycarbonylthiophene with phosphorus (III) tribromide. These heterocyclizations can be carried out in the basic medium and under mild conditions. The end reaction products were studied by means of chemical analysis, 1H and 31P NMR spectroscopy.
dc.format.extent145-149
dc.language.isoen
dc.publisherВидавництво Львівської політехніки
dc.publisherLviv Politechnic Publishing House
dc.relation.ispartofChemistry & Chemical Technology, 2 (13), 2019
dc.relation.urihttps://doi.org/10.1016/S0040-4039(00)61405-3
dc.relation.urihttps://doi.org/10.1002/hc.21163
dc.relation.urihttps://doi.org/10.1039/C2JM33526C
dc.relation.urihttps://doi.org/10.1002/chem.200700399
dc.relation.urihttps://doi.org/10.1021/ol052911p
dc.relation.urihttps://doi.org/10.1002/chem.200500152
dc.relation.urihttps://doi.org/10.1080/10426509308045639
dc.relation.urihttps://doi.org/10.3987/COM-97-7930
dc.relation.urihttps://doi.org/10.1002/cber.19761090137
dc.relation.urihttps://doi.org/10.1016/S0022-328X(00)93116-4
dc.relation.urihttps://doi.org/10.1016/S0040-4039(00)77610-6
dc.relation.urihttps://doi.org/10.1016/S0040-4039(00)61404-1
dc.relation.urihttps://doi.org/10.1080/10426509608054662
dc.relation.urihttps://doi.org/10.3987/COM-97-7911
dc.relation.urihttps://doi.org/10.1016/S0040-4020(01)87270-7
dc.relation.urihttps://doi.org/10.1139/V09-108
dc.relation.urihttps://doi.org/10.1002/asia.201000196
dc.relation.urihttps://doi.org/10.1080/03086648208073110
dc.relation.urihttps://doi.org/10.1002/zaac.19774370107
dc.subjectтіофен
dc.subjectазафосфінін
dc.subjectоксазафосфінін
dc.subjectанельовані цикли
dc.subjectгетероцикл
dc.subjectфосфорилювання
dc.subjectthiophene
dc.subjectazaphosphinine
dc.subjectoxazaphosphinine
dc.subjectfused rings
dc.subjectheterocycle
dc.subjectphosphorylation
dc.titleSynthesis of Annelated P- and N-containing Heterocycles Based on Methyl 5-Aminothiophene-2-Carboxylate Derivatives
dc.title.alternativeСинтез анельованих гетероциклів, що містять P- і N-атоми, на основі похідних 5-аміно-2-метоксикарбонілтіофену
dc.typeArticle
dc.rights.holder© Національний університет „Львівська політехніка“, 2019
dc.rights.holder© Kovaleva S., Mayboroda O., Simurova N., Mazur L., 2019
dc.contributor.affiliationNational University of Food Technologies
dc.format.pages5
dc.identifier.citationenSynthesis of Annelated P- and N-containing Heterocycles Based on Methyl 5-Aminothiophene-2-Carboxylate Derivatives / Svitlana Kovaleva, Olena Mayboroda, Natalia Simurova, Larysa Mazur // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2019. — Vol 13. — No 2. — P. 145–149.
dc.relation.references1. Mathey F.: Phosphorus-Carbon Heterocyclic Chemistry. Pergamon Press, Oxford 2001.
dc.relation.references2. Ishii A., Yoshioka R., Nakayama J., HoshinoM.: Tetrahedron Lett., 1993, 34, 8259. https://doi.org/10.1016/S0040-4039(00)61405-3
dc.relation.references3. Uchiyama Y., Kawaguchi T., Kuroda K.: Heteroatom. Chem., 2014, 25, 326. https://doi.org/10.1002/hc.21163
dc.relation.references4. Kondo R., Yasuda T., Yang Y., Kim J. Y., Adachi C.: J. Mater. Chem., 2012, 22, 16810. https://doi.org/10.1039/C2JM33526C
dc.relation.references5. Dienes Y., Durben S., Karpati T. et al.: Chem.-Eur. J., 2007, 13, 7487. https://doi.org/10.1002/chem.200700399
dc.relation.references6. Neumann T., Dienes Y., Baumgartner T.: Org. Lett., 2006, 8, 495. https://doi.org/10.1021/ol052911p
dc.relation.references7. Baumgartner T., BergmansW., Karpati T. et al.: Chem.-Eur. J., 2005, 11, 4687. https://doi.org/10.1002/chem.200500152
dc.relation.references8. Ishii A., Takaki I., Nakayama J., HoshinoM.: Phosphorus Sulfur, 1993, 77, 149. https://doi.org/10.1080/10426509308045639
dc.relation.references9. Yasuike S., Nakashima F, Kurita J., Tsuchiya T.: Heterocycles, 1997, 45, 1899. https://doi.org/10.3987/COM-97-7930
dc.relation.references10. Fenske D., Longer K., HeymannM., Becher H.-J.: Chem. Ber., 1976, 109, 359. https://doi.org/10.1002/cber.19761090137
dc.relation.references11. Lampin J., Mathey F.: J. Organomet. Chem., 1974, 71, 239. https://doi.org/10.1016/S0022-328X(00)93116-4
dc.relation.references12. Ishii A., Tsuchiya Т., Nakayama J., HoshinoM.: Tetrahedron Lett., 1993, 34, 2347. https://doi.org/10.1016/S0040-4039(00)77610-6
dc.relation.references13. Ishii A., Takaki I., Nakayama J., HoshinoM.: Tetrahedron Lett., 1993, 34, 8255. https://doi.org/10.1016/S0040-4039(00)61404-1
dc.relation.references14. Ishii A., Yoshioka R„ Nakayama J., HoshinoM.: Tetrahedron Lett., 1993, 34, 8259. https://doi.org/10.1016/S0040-4039(00)61405-3
dc.relation.references15. Combes C., Plenat F., Cristau H.-J.: Phosphorus, Sulfur, Silicon. Relat. Elem., 1996, 111, 33. https://doi.org/10.1080/10426509608054662
dc.relation.references16. Yasuike S., Nakashima F., Kurita J., Tsuchiya T.: Heterocycles, 1997, 45, 1899. https://doi.org/10.3987/COM-97-7930
dc.relation.references17. Yasuike S., Kurita J., Tsuchiya T.: Heterocycles, 1997, 45, 1891. https://doi.org/10.3987/COM-97-7911
dc.relation.references18. Dotz K., Tiriliomis A., Harms K.: Tetrahedron, 1993, 49, 5577. https://doi.org/10.1016/S0040-4020(01)87270-7
dc.relation.references19. Ren Y., Linder T., Baumgartner T.: Can. J. Chem., 2009, 87, 1222. https://doi.org/10.1139/V09-108
dc.relation.references20. Ren Y., Baumgartner T.: Chem.-Asian J., 2010, 5, 1918. https://doi.org/10.1002/asia.201000196
dc.relation.references21. Kovaleva S., Chubaruk N., Tolmachov A., Pinchuk A.: Khim. Heterocycl. Soed., 2001, 9, 1287.
dc.relation.references22. Kovaleva S., Simurova N., Mayboroda E.: Ukr. Khim. Zh., 2016, 82, 91.
dc.relation.references23. Schmidpeter A., Gross J., Schrenk E., Sheldrick N.: Phosphorus Sulfur, 1982, 14, 49. https://doi.org/10.1080/03086648208073110
dc.relation.references24. Fluck E., VargausM.: Zeitschrift für anorganische und allgemeine Chemie., 1977, 437, 53. https://doi.org/10.1002/zaac.19774370107
dc.relation.references25. Volochnuk D., Pushechnikov A., Krotko D. et al.: Synthesis, 2003, 6, 906.
dc.relation.referencesen1. Mathey F., Phosphorus-Carbon Heterocyclic Chemistry. Pergamon Press, Oxford 2001.
dc.relation.referencesen2. Ishii A., Yoshioka R., Nakayama J., HoshinoM., Tetrahedron Lett., 1993, 34, 8259. https://doi.org/10.1016/S0040-4039(00)61405-3
dc.relation.referencesen3. Uchiyama Y., Kawaguchi T., Kuroda K., Heteroatom. Chem., 2014, 25, 326. https://doi.org/10.1002/hc.21163
dc.relation.referencesen4. Kondo R., Yasuda T., Yang Y., Kim J. Y., Adachi C., J. Mater. Chem., 2012, 22, 16810. https://doi.org/10.1039/P.2JM33526C
dc.relation.referencesen5. Dienes Y., Durben S., Karpati T. et al., Chem.-Eur. J., 2007, 13, 7487. https://doi.org/10.1002/chem.200700399
dc.relation.referencesen6. Neumann T., Dienes Y., Baumgartner T., Org. Lett., 2006, 8, 495. https://doi.org/10.1021/ol052911p
dc.relation.referencesen7. Baumgartner T., BergmansW., Karpati T. et al., Chem.-Eur. J., 2005, 11, 4687. https://doi.org/10.1002/chem.200500152
dc.relation.referencesen8. Ishii A., Takaki I., Nakayama J., HoshinoM., Phosphorus Sulfur, 1993, 77, 149. https://doi.org/10.1080/10426509308045639
dc.relation.referencesen9. Yasuike S., Nakashima F, Kurita J., Tsuchiya T., Heterocycles, 1997, 45, 1899. https://doi.org/10.3987/COM-97-7930
dc.relation.referencesen10. Fenske D., Longer K., HeymannM., Becher H.-J., Chem. Ber., 1976, 109, 359. https://doi.org/10.1002/cber.19761090137
dc.relation.referencesen11. Lampin J., Mathey F., J. Organomet. Chem., 1974, 71, 239. https://doi.org/10.1016/S0022-328X(00)93116-4
dc.relation.referencesen12. Ishii A., Tsuchiya T., Nakayama J., HoshinoM., Tetrahedron Lett., 1993, 34, 2347. https://doi.org/10.1016/S0040-4039(00)77610-6
dc.relation.referencesen13. Ishii A., Takaki I., Nakayama J., HoshinoM., Tetrahedron Lett., 1993, 34, 8255. https://doi.org/10.1016/S0040-4039(00)61404-1
dc.relation.referencesen14. Ishii A., Yoshioka R" Nakayama J., HoshinoM., Tetrahedron Lett., 1993, 34, 8259. https://doi.org/10.1016/S0040-4039(00)61405-3
dc.relation.referencesen15. Combes C., Plenat F., Cristau H.-J., Phosphorus, Sulfur, Silicon. Relat. Elem., 1996, 111, 33. https://doi.org/10.1080/10426509608054662
dc.relation.referencesen16. Yasuike S., Nakashima F., Kurita J., Tsuchiya T., Heterocycles, 1997, 45, 1899. https://doi.org/10.3987/COM-97-7930
dc.relation.referencesen17. Yasuike S., Kurita J., Tsuchiya T., Heterocycles, 1997, 45, 1891. https://doi.org/10.3987/COM-97-7911
dc.relation.referencesen18. Dotz K., Tiriliomis A., Harms K., Tetrahedron, 1993, 49, 5577. https://doi.org/10.1016/S0040-4020(01)87270-7
dc.relation.referencesen19. Ren Y., Linder T., Baumgartner T., Can. J. Chem., 2009, 87, 1222. https://doi.org/10.1139/V09-108
dc.relation.referencesen20. Ren Y., Baumgartner T., Chem.-Asian J., 2010, 5, 1918. https://doi.org/10.1002/asia.201000196
dc.relation.referencesen21. Kovaleva S., Chubaruk N., Tolmachov A., Pinchuk A., Khim. Heterocycl. Soed., 2001, 9, 1287.
dc.relation.referencesen22. Kovaleva S., Simurova N., Mayboroda E., Ukr. Khim. Zh., 2016, 82, 91.
dc.relation.referencesen23. Schmidpeter A., Gross J., Schrenk E., Sheldrick N., Phosphorus Sulfur, 1982, 14, 49. https://doi.org/10.1080/03086648208073110
dc.relation.referencesen24. Fluck E., VargausM., Zeitschrift für anorganische und allgemeine Chemie., 1977, 437, 53. https://doi.org/10.1002/zaac.19774370107
dc.relation.referencesen25. Volochnuk D., Pushechnikov A., Krotko D. et al., Synthesis, 2003, 6, 906.
dc.citation.issue2
dc.citation.spage145
dc.citation.epage149
dc.coverage.placenameЛьвів
dc.coverage.placenameLviv
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