| DC Field | Value | Language |
|---|
| dc.contributor.author | Baranovskyi, Vitaliy | |
| dc.contributor.author | Symchak, Ruslan | |
| dc.contributor.author | Pokryshko, Olena | |
| dc.contributor.author | Klymnyuk, Sergiy | |
| dc.contributor.author | Grishchuk, Bogdan | |
| dc.date.accessioned | 2019-06-21T07:58:04Z | - |
| dc.date.available | 2019-06-21T07:58:04Z | - |
| dc.date.created | 2018-01-20 | |
| dc.date.issued | 2018-01-20 | |
| dc.identifier.citation | Arylsubstituted halogen(thiocyanato)amides containing 4-acetylphenyl fragment. Synthesis, cyclization and antimicrobial properties / Vitaliy Baranovskyi, Ruslan Symchak, Olena Pokryshko, Sergiy Klymnyuk, Bogdan Grishchuk // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2018. — Vol 12. — No 4. — P. 447–450. | |
| dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/45209 | - |
| dc.description.abstract | Купрокаталітичним аніонарилюванням
амідів акрилової і метакрилової кислот солями 4-ацетилфе-
нілдіазонію синтезовані 3-(4-ацетилфеніл)-(2-метил)-2-хлоро
(бромо, тіоціанато)пропанаміди. Циклізацією тіоціанато-
амідів одержані арилзаміщені 2-амінотіазол-4(5Н)-они з
ацетофеноновим фрагментом. Досліджено протибакте-
ріальну та протигрибкову активність синтезованих сполук. | |
| dc.description.abstract | 13-(4-Acetylphenyl)-(2-methyl)-2-chloro(bromo,
thiocyanato)propanamides have been obtained via copper
catalytic anionarylation of acrylic and methacrylic acids
amides by 4-acetylphenyldiazonium salts. 5-(4-Acetylphenyl)
substituted 2-aminothiazol-4(5H)-ones were
synthesized by cyclisation of thiocyanatoamides. All
synthesized compounds were tested for their antibacterial
and antomycotic activity. | |
| dc.format.extent | 447-450 | |
| dc.language.iso | en | |
| dc.publisher | Lviv Politechnic Publishing House | |
| dc.relation.ispartof | Chemistry & Chemical Technology, 4 (12), 2018 | |
| dc.relation.uri | https://doi.org/10.1042/bj1520233 | |
| dc.relation.uri | https://doi.org/10.3390/molecules15128813 | |
| dc.relation.uri | https://doi.org/10.1039/C5MD00357A | |
| dc.relation.uri | https://doi.org/10.1134/S1070363209020170 | |
| dc.relation.uri | https://doi.org/10.1134/S1070363214080106 | |
| dc.relation.uri | https://doi.org/10.1007/s11094-011-0673-0 | |
| dc.relation.uri | https://doi.org/10.1007/s11094-013-0949-7 | |
| dc.relation.uri | https://doi.org/10.1007/s11094-016-1484-0 | |
| dc.relation.uri | https://doi.org/10.23939/chcht09.02.193 | |
| dc.subject | аніонарилювання | |
| dc.subject | аміди акрилової і метакрилової кислот | |
| dc.subject | солі 4-ацетилфенілдіазонію | |
| dc.subject | 5-арилза- міщені 2-амінотіазол-4(5Н)-они | |
| dc.subject | протимікробна активність | |
| dc.subject | anionarylation | |
| dc.subject | acrylic and methacrylic acids amides | |
| dc.subject | 4-acetylphenyldiazonium salts | |
| dc.subject | 5-arylsubstituted 2-aminothiazol-4(5H)-ones | |
| dc.subject | antimicrobial activity | |
| dc.title | Arylsubstituted halogen(thiocyanato)amides containing 4-acetylphenyl fragment. Synthesis, cyclization and antimicrobial properties | |
| dc.title.alternative | Арилзаміщені галогено(тіоціанато)аміди, що містять 4-ацетилфенільний фрагмент. Синтез, циклізація та протимікробні властивості | |
| dc.type | Article | |
| dc.rights.holder | © Національний університет „Львівська політехніка“, 2018 | |
| dc.rights.holder | ©Baranovskyi V., Symchak R., Pokryshko O., Klymnyuk S.,Grishchuk B., 2018 | |
| dc.contributor.affiliation | Ternopil V. Hnatyuk National Pedagogical University | |
| dc.contributor.affiliation | I. Ya. Horbachevsky Ternopil State Medical University | |
| dc.format.pages | 4 | |
| dc.identifier.citationen | Arylsubstituted halogen(thiocyanato)amides containing 4-acetylphenyl fragment. Synthesis, cyclization and antimicrobial properties / Vitaliy Baranovskyi, Ruslan Symchak, Olena Pokryshko, Sergiy Klymnyuk, Bogdan Grishchuk // Chemistry & Chemical Technology. — Lviv : Lviv Politechnic Publishing House, 2018. — Vol 12. — No 4. — P. 447–450. | |
| dc.relation.references | [1] O'Neil M. (Ed.): The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 15th edn. Merck and Co. Inc., Cambridge 2013. | |
| dc.relation.references | [2] Cripps R.: Biochem J., 1975, 152, 233.https://doi.org/10.1042/bj1520233 | |
| dc.relation.references | [3] Salas P., Soto A., Carretero A. et al.:Molecules, 2010, 15,8813. https://doi.org/10.3390/molecules15128813 | |
| dc.relation.references | [4] Pharmaceutical Manufacturing Encyclopedia. William Andrew Publishing, Norwich, NY 2007. | |
| dc.relation.references | [5] Shen Y., Li B., Xu H. et al.: Pharmazie, 2013, 68, 307. | |
| dc.relation.references | [6] Wang Z., Li X., Xu W. et al.:Med. Chem. Commun., 2015, 6,2146. https://doi.org/10.1039/C5MD00357A | |
| dc.relation.references | [7] Baranovskii V., Simchak R., Grishchuk B.: Russ. J. Gen. Chem.,2009, 79, 269. https://doi.org/10.1134/S1070363209020170 | |
| dc.relation.references | [8] Baranovskii V., Yatsyuk V., Grishchuk B.: Russ. J. Gen. Chem.,2014, 84, 1505. https://doi.org/10.1134/S1070363214080106 | |
| dc.relation.references | [9] Grishchuk B., Baranovskii V., Klymnyuk S. et al.: Pharm. Chem. J., 2011, 45, 532. https://doi.org/10.1007/s11094-011-0673-0 | |
| dc.relation.references | [10] Grishchuk B., Simchak R., Baranovskii V. et al.: Pharm. Chem. J., 2013, 47, 307. https://doi.org/10.1007/s11094-013-0949-7 | |
| dc.relation.references | [11] Grishchuk B., Yatsyuk V., Baranovskii V. et al.: Pharm. Chem. J., 2016, 50, 534. https://doi.org/10.1007/s11094-016-1484-0 | |
| dc.relation.references | [12] Yatsyuk V., Pokryshko O., Yaniv Z. et al.: Chem. Chem. Technol., 2015, 9, 193. https://doi.org/10.23939/chcht09.02.193 | |
| dc.relation.references | [13] Grishchuk B., Baranovskyi V., Klymnyuk S.: Pharmac. Rev.,2011, 4, 117. | |
| dc.relation.referencesen | [1] O'Neil M. (Ed.): The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 15th edn. Merck and Co. Inc., Cambridge 2013. | |
| dc.relation.referencesen | [2] Cripps R., Biochem J., 1975, 152, 233.https://doi.org/10.1042/bj1520233 | |
| dc.relation.referencesen | [3] Salas P., Soto A., Carretero A. et al.:Molecules, 2010, 15,8813. https://doi.org/10.3390/molecules15128813 | |
| dc.relation.referencesen | [4] Pharmaceutical Manufacturing Encyclopedia. William Andrew Publishing, Norwich, NY 2007. | |
| dc.relation.referencesen | [5] Shen Y., Li B., Xu H. et al., Pharmazie, 2013, 68, 307. | |
| dc.relation.referencesen | [6] Wang Z., Li X., Xu W. et al.:Med. Chem. Commun., 2015, 6,2146. https://doi.org/10.1039/P.5MD00357A | |
| dc.relation.referencesen | [7] Baranovskii V., Simchak R., Grishchuk B., Russ. J. Gen. Chem.,2009, 79, 269. https://doi.org/10.1134/S1070363209020170 | |
| dc.relation.referencesen | [8] Baranovskii V., Yatsyuk V., Grishchuk B., Russ. J. Gen. Chem.,2014, 84, 1505. https://doi.org/10.1134/S1070363214080106 | |
| dc.relation.referencesen | [9] Grishchuk B., Baranovskii V., Klymnyuk S. et al., Pharm. Chem. J., 2011, 45, 532. https://doi.org/10.1007/s11094-011-0673-0 | |
| dc.relation.referencesen | [10] Grishchuk B., Simchak R., Baranovskii V. et al., Pharm. Chem. J., 2013, 47, 307. https://doi.org/10.1007/s11094-013-0949-7 | |
| dc.relation.referencesen | [11] Grishchuk B., Yatsyuk V., Baranovskii V. et al., Pharm. Chem. J., 2016, 50, 534. https://doi.org/10.1007/s11094-016-1484-0 | |
| dc.relation.referencesen | [12] Yatsyuk V., Pokryshko O., Yaniv Z. et al., Chem. Chem. Technol., 2015, 9, 193. https://doi.org/10.23939/chcht09.02.193 | |
| dc.relation.referencesen | [13] Grishchuk B., Baranovskyi V., Klymnyuk S., Pharmac. Rev.,2011, 4, 117. | |
| dc.citation.journalTitle | Chemistry & Chemical Technology | |
| dc.citation.volume | 12 | |
| dc.citation.issue | 4 | |
| dc.citation.spage | 447 | |
| dc.citation.epage | 450 | |
| dc.coverage.placename | Lviv | |
| Appears in Collections: | Chemistry & Chemical Technology. – 2018. – Vol. 12, No. 4
|
