Design, Synthesis, and in Vitro Evaluation of Thieno[A]dibenzothiophene Derivatives
dc.authorid | Konus, Metin/0000-0002-9953-1375 | |
dc.authorid | Yilmaz, Can/0000-0002-0028-6614 | |
dc.authorid | Kavak, Emrah/0000-0002-6161-2030 | |
dc.authorid | Kivrak, Arif/0000-0003-4770-2686 | |
dc.authorid | Kurt Kizildogan, Aslihan/0000-0002-9323-0993 | |
dc.authorscopusid | 56387553800 | |
dc.authorscopusid | 57203329350 | |
dc.authorscopusid | 56891345500 | |
dc.authorscopusid | 57192710504 | |
dc.authorscopusid | 57221517895 | |
dc.authorscopusid | 8694518300 | |
dc.authorwosid | Yilmaz, Can/Grs-2754-2022 | |
dc.authorwosid | Kivrak, Arif/Aaq-8432-2021 | |
dc.authorwosid | Kurt-Kizildogan, Aslihan/Jce-2182-2023 | |
dc.authorwosid | Kavak, Emrah/Gls-1399-2022 | |
dc.authorwosid | Kivrak, Arif/W-2196-2017 | |
dc.authorwosid | Kurt Kizildogan, Aslihan/A-1199-2019 | |
dc.contributor.author | Konus, Metin | |
dc.contributor.author | Algso, Muheb A. S. | |
dc.contributor.author | Kavak, Emrah | |
dc.contributor.author | Kurt-Kizildogan, Aslihan | |
dc.contributor.author | Yilmaz, Can | |
dc.contributor.author | Kivrak, Arif | |
dc.date.accessioned | 2025-05-10T17:04:04Z | |
dc.date.available | 2025-05-10T17:04:04Z | |
dc.date.issued | 2020 | |
dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
dc.department-temp | [Algso, Muheb A. S.; Kavak, Emrah; Kivrak, Arif] Van Yuzuncu Yil Univ, Dept Chem, TR-65080 Van, Turkey; [Konus, Metin; Yilmaz, Can] Van Yuzuncu Yil Univ, Dept Mol Biol & Genet, TR-65080 Van, Turkey; [Kurt-Kizildogan, Aslihan] Ondokuz Mayis Univ, Fac Agr, Dept Agr Biotechnol, TR-55139 Samsun, Turkey | en_US |
dc.description | Konus, Metin/0000-0002-9953-1375; Yilmaz, Can/0000-0002-0028-6614; Kavak, Emrah/0000-0002-6161-2030; Kivrak, Arif/0000-0003-4770-2686; Kurt Kizildogan, Aslihan/0000-0002-9323-0993 | en_US |
dc.description.abstract | A variety of highly substituted thieno[2,3-a]dibenzothiophenes and thieno[3,2-a]dibenzothiophenes are readily prepared via cascade electrophilic cyclization reaction. The reaction was tolerated a variety of compounds. In the present study, antimicrobial and antifungal activities were investigated for all synthesized molecules against A. niger ATCC 16404, C. albicans ATCC 10231, S. aureus ATCC 25923 and B. subtilis ATCC 6633, respectively. | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey [115Z020] | en_US |
dc.description.sponsorship | The authors thank to The Scientific and Technological Research Council of Turkey (Project No: 115Z020). The author(s) would like to acknowledge networking contribution by the COST Action CM1407 "Challenging organic syntheses inspired by nature from natural products chemistry to drug discovery". | en_US |
dc.description.woscitationindex | Science Citation Index Expanded | |
dc.identifier.doi | 10.1002/slct.202000685 | |
dc.identifier.endpage | 3709 | en_US |
dc.identifier.issn | 2365-6549 | |
dc.identifier.issue | 12 | en_US |
dc.identifier.scopus | 2-s2.0-85082553664 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 3700 | en_US |
dc.identifier.uri | https://doi.org/10.1002/slct.202000685 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14720/5901 | |
dc.identifier.volume | 5 | en_US |
dc.identifier.wos | WOS:000522352200030 | |
dc.identifier.wosquality | Q3 | |
dc.language.iso | en | en_US |
dc.publisher | Wiley-v C H verlag Gmbh | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Antibacterial | en_US |
dc.subject | Antifungal | en_US |
dc.subject | Cascade Reaction | en_US |
dc.subject | Electrophilic Cyclization | en_US |
dc.subject | Thieno[A]Dibenzothiophenes | en_US |
dc.title | Design, Synthesis, and in Vitro Evaluation of Thieno[A]dibenzothiophene Derivatives | en_US |
dc.type | Article | en_US |