Yayın:
Synthesis, characterization and biological activities evaluation of novel sulfanyl derivatives

Basit Görünüm
dc.contributor.authorSaraç, Kamuran
dc.contributor.authorOrek, Cahit
dc.contributor.authorKoparir, Metin
dc.date.accessioned2026-01-04T13:29:21Z
dc.date.issued2019-10-03
dc.description.abstractA novel series of 1-(3-Methyl-3-mesityl)-cyclobutyl-2-{[5-(2-fluorophenyl)-4-(aryl-alkyl)-4H-[1,2,4]triazol-3-yl]sulfanyl}-ethanone compounds were synthesized by a condensation reaction. The new compounds were characterized by elemental analyses, FT-IR and <sup>1</sup>H, <sup>13</sup>C NMR techniques. The antioxidant and antibacterial properties of the synthesized compounds were also investigated. The in vitro antioxidant and antibacterial activities of the newly synthesized compounds were measured, and they were found to exhibit significantly high antioxidant activity.
dc.description.urihttps://doi.org/10.1080/10426507.2019.1672692
dc.description.urihttps://dx.doi.org/10.6084/m9.figshare.9933929.v1
dc.description.urihttps://dx.doi.org/10.6084/m9.figshare.9933929
dc.description.urihttps://dx.doi.org/10.1080/10426507.2019.1672692
dc.identifier.doi10.1080/10426507.2019.1672692
dc.identifier.eissn1563-5325
dc.identifier.endpage225
dc.identifier.issn1042-6507
dc.identifier.openairedoi_dedup___::2fd89e3cad001a126c0fcb54a3f10c24
dc.identifier.orcid0000-0002-3854-1537
dc.identifier.orcid0000-0003-1031-783x
dc.identifier.scopus2-s2.0-85074037180
dc.identifier.startpage218
dc.identifier.urihttps://hdl.handle.net/20.500.12597/37527
dc.identifier.volume195
dc.identifier.wos000489426700001
dc.language.isoeng
dc.publisherInforma UK Limited
dc.relation.ispartofPhosphorus, Sulfur, and Silicon and the Related Elements
dc.rightsOPEN
dc.titleSynthesis, characterization and biological activities evaluation of novel sulfanyl derivatives
dc.typeArticle
dspace.entity.typePublication
local.api.response{"authors":[{"fullName":"Saraç, Kamuran","name":"Kamuran","surname":"Saraç","rank":1,"pid":null},{"fullName":"Orek, Cahit","name":"Cahit","surname":"Orek","rank":2,"pid":{"id":{"scheme":"orcid","value":"0000-0002-3854-1537"},"provenance":null}},{"fullName":"Koparir, Metin","name":"Metin","surname":"Koparir","rank":3,"pid":{"id":{"scheme":"orcid","value":"0000-0003-1031-783x"},"provenance":null}}],"openAccessColor":null,"publiclyFunded":false,"type":"publication","language":{"code":"eng","label":"English"},"countries":null,"subjects":[{"subject":{"scheme":"FOS","value":"0301 basic medicine"},"provenance":null},{"subject":{"scheme":"FOS","value":"0303 health sciences"},"provenance":null},{"subject":{"scheme":"FOS","value":"03 medical and health sciences"},"provenance":null}],"mainTitle":"Synthesis, characterization and biological activities evaluation of novel sulfanyl derivatives","subTitle":null,"descriptions":["A novel series of 1-(3-Methyl-3-mesityl)-cyclobutyl-2-{[5-(2-fluorophenyl)-4-(aryl-alkyl)-4H-[1,2,4]triazol-3-yl]sulfanyl}-ethanone compounds were synthesized by a condensation reaction. The new compounds were characterized by elemental analyses, FT-IR and <sup>1</sup>H, <sup>13</sup>C NMR techniques. The antioxidant and antibacterial properties of the synthesized compounds were also investigated. The in vitro antioxidant and antibacterial activities of the newly synthesized compounds were measured, and they were found to exhibit significantly high antioxidant activity."],"publicationDate":"2019-10-03","publisher":"Informa UK Limited","embargoEndDate":null,"sources":["Crossref"],"formats":null,"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_abf2","label":"OPEN","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":{"name":"Phosphorus, Sulfur, and Silicon and the Related Elements","issnPrinted":"1042-6507","issnOnline":"1563-5325","issnLinking":null,"ep":"225","iss":null,"sp":"218","vol":"195","edition":null,"conferencePlace":null,"conferenceDate":null},"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"doi_dedup___::2fd89e3cad001a126c0fcb54a3f10c24","originalIds":["10.1080/10426507.2019.1672692","50|doiboost____|2fd89e3cad001a126c0fcb54a3f10c24","50|datacite____::17675ecd66ce59d1841ea12aced6e1f0","10.6084/m9.figshare.9933929.v1","50|datacite____::31fae59cbde6050c93ce537d548f35d2","10.6084/m9.figshare.9933929","2977634685"],"pids":[{"scheme":"doi","value":"10.1080/10426507.2019.1672692"},{"scheme":"doi","value":"10.6084/m9.figshare.9933929.v1"},{"scheme":"doi","value":"10.6084/m9.figshare.9933929"}],"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":1,"influence":2.5635418e-9,"popularity":2.07806e-9,"impulse":1,"citationClass":"C5","influenceClass":"C5","impulseClass":"C5","popularityClass":"C5"}},"instances":[{"pids":[{"scheme":"doi","value":"10.1080/10426507.2019.1672692"}],"type":"Article","urls":["https://doi.org/10.1080/10426507.2019.1672692"],"publicationDate":"2019-10-03","refereed":"peerReviewed"},{"pids":[{"scheme":"doi","value":"10.6084/m9.figshare.9933929.v1"}],"license":"CC BY","type":"Other literature type","urls":["https://dx.doi.org/10.6084/m9.figshare.9933929.v1"],"publicationDate":"2019-01-01","refereed":"nonPeerReviewed"},{"pids":[{"scheme":"doi","value":"10.6084/m9.figshare.9933929"}],"license":"CC BY","type":"Other literature type","urls":["https://dx.doi.org/10.6084/m9.figshare.9933929"],"publicationDate":"2019-01-01","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.1080/10426507.2019.1672692"},{"scheme":"mag_id","value":"2977634685"}],"type":"Article","urls":["https://dx.doi.org/10.1080/10426507.2019.1672692"],"refereed":"nonPeerReviewed"}],"isGreen":true,"isInDiamondJournal":false}
local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus

Dosyalar

Koleksiyonlar

Publications