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dc.contributor.authorVatansever, Erol Can
dc.contributor.authorKilic, Kubra
dc.contributor.authorOzer, Merve Sinem
dc.contributor.authorKoza, Gani
dc.contributor.authorMenges, Nurettin
dc.contributor.authorBalci, Metin
dc.date.accessioned2019-11-24T20:38:30Z
dc.date.available2019-11-24T20:38:30Z
dc.date.issued2015
dc.identifier.issn0040-4039
dc.identifier.urihttps://dx.doi.org/10.1016/j.tetlet.2015.07.090
dc.identifier.urihttps://hdl.handle.net/20.500.12513/2534
dc.descriptionWOS: 000362533900004en_US
dc.description.abstractA concise and regioselective approach for the synthesis of 2,3-disubstituted thiophene derivatives has been developed. The synthetic strategy relies on the reaction of an in situ generated 2-mercaptoacetaldehyde with various alkynones. Furthermore, we calculated the energy gap between the HOMO and the LUMO orbitals of all compounds and observed that the introduction of a strong electron-withdrawing group decreased the HOMO-LUMO energy gap. (C) 2015 Elsevier Ltd. All rights reserved.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TBAG-112 T360]; Turkish Academy of Sciences (TUBA)Turkish Academy of Sciences; Yuzuncu Yil UniversityYuzuncu Yil University [YYU-BAP-2014-ECZ-B170]; Middle East Technical University (METU)en_US
dc.description.sponsorshipFinancial support from the Scientific and Technological Research Council of Turkey (TUBITAK, Grant No. TBAG-112 T360), the Turkish Academy of Sciences (TUBA), Middle East Technical University (METU), and Yuzuncu Yil University (Grant No. YYU-BAP-2014-ECZ-B170) are gratefully acknowledged.en_US
dc.language.isoengen_US
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDen_US
dc.relation.isversionof10.1016/j.tetlet.2015.07.090en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAlkynesen_US
dc.subjectCyclizationen_US
dc.subjectAlkynonesen_US
dc.subject2-Mercaptoacetaldehydeen_US
dc.subject2,3-Disubstituted thiophenesen_US
dc.titleIntermolecular heterocyclization of alkynones with 2-mercaptoacetaldehyde under metal-free conditions: synthesis of 2,3-disubstituted thiophenesen_US
dc.typearticleen_US
dc.relation.journalTETRAHEDRON LETTERSen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.identifier.volume56en_US
dc.identifier.issue40en_US
dc.identifier.startpage5386en_US
dc.identifier.endpage5389en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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