Synthesis of Novel Benzothiophene Derivatives Via Cyclization Reactions

dc.contributor.author Hama, A. K.
dc.contributor.author Algso, M. A. S.
dc.contributor.author Kavak, E.
dc.contributor.author Kivrak, A.
dc.date.accessioned 2025-05-10T17:09:12Z
dc.date.available 2025-05-10T17:09:12Z
dc.date.issued 2020
dc.description Kavak, Emrah/0000-0002-6161-2030; Kivrak, Arif/0000-0003-4770-2686 en_US
dc.description.abstract The Sonogashira cross coupling reaction of 2-bromo-5-(4-methoxyphenyl)thiophene and 1-ethynyl-2-(methylsulfanyl)benzene gave 2-(4-methoxyphenyl)-5-{[2-(methylsulfanyl)phenyl]ethynyl}thiophene which was subjected to electrophilic cyclization by the action of iodine to obtain 3-iodo-2-[5-(4-methoxyphenyl)thiophen-2-yl]-1-benzothiophene. Stille and Sonogashira coupling reactions of the latter afforded a series of new 3-substituted 2-[5-(4-methoxyphenyl)thiophen-2-yl]-1-benzothiophene derivatives of potential pharmacological interest. en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkey [115Z020]; Van Yuzuncu Yil University [FDP-2018-6862] en_US
dc.description.sponsorship The authors thank the Scientific and Technological Research Council of Turkey (project no. 115Z020) for financial supporting of reactant and reagents and Van Yuzuncu Yil University (project no. FDP-2018-6862) for financial supporting of solvents, glassware, and salts. en_US
dc.identifier.doi 10.1134/S1070428020070222
dc.identifier.issn 1070-4280
dc.identifier.issn 1608-3393
dc.identifier.scopus 2-s2.0-85090767500
dc.identifier.uri https://doi.org/10.1134/S1070428020070222
dc.identifier.uri https://hdl.handle.net/20.500.14720/7079
dc.language.iso en en_US
dc.publisher Maik Nauka/interperiodica/springer en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Benzothiophenes en_US
dc.subject Heteroaromatic Compounds en_US
dc.subject Cyclization Reactions en_US
dc.subject Coupling Reactions en_US
dc.title Synthesis of Novel Benzothiophene Derivatives Via Cyclization Reactions en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Kavak, Emrah/0000-0002-6161-2030
gdc.author.id Kivrak, Arif/0000-0003-4770-2686
gdc.author.scopusid 57218921206
gdc.author.scopusid 57203329350
gdc.author.scopusid 56891345500
gdc.author.scopusid 8694518300
gdc.author.wosid Kivrak, Arif/Aaq-8432-2021
gdc.author.wosid Kavak, Emrah/Gls-1399-2022
gdc.author.wosid Kivrak, Arif/W-2196-2017
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Hama, A. K.; Algso, M. A. S.; Kavak, E.; Kivrak, A.] Van Yuzuncu Yil Univ, Dept Chem, TR-65080 Van, Turkey en_US
gdc.description.endpage 1278 en_US
gdc.description.issue 7 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 1272 en_US
gdc.description.volume 56 en_US
gdc.description.woscitationindex Science Citation Index Expanded - Index Chemicus
gdc.description.wosquality Q4
gdc.identifier.wos WOS:000567893800022
gdc.index.type WoS
gdc.index.type Scopus

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