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dc.contributor.advisorİyidoğan, Ayşegül
dc.contributor.authorÇevik, Caner
dc.date.accessioned2020-12-29T13:29:55Z
dc.date.available2020-12-29T13:29:55Z
dc.date.submitted2015
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/427318
dc.description.abstractBu çalışmada, (S)-(+)-1,2,3,4-tetrahidro-1-naftilamin/(R)-(-)-1,2,3,4-tetrahidro-1-naftilamin dietileterli ortamda çeşitli sübstitüe benzoil klorürlerle oda sıcaklığında reaksiyona sokularak 12 kiral amit türevli bileşik [1a-f ve 2a-f] elde edildi.Gerçekleştirilen tüm reaksiyonlar İnce Tabaka Kromatografisi (İTK) ile izlendi. Sentezlenen bileşiklerinin yapıları fiziksel ve kimyasal yöntemlerin yanı sıra UV-Vis, FT IR, 1H NMR, 13C NMR, MS gibi spektroskopik yöntemler ve elementel analiz (C, H, N, S) tekniği yardımı ile aydınlatıldı.
dc.description.abstractIn present work, we synthesized twelwe chiral amide derivatives [1a-f and 2a-f] in high yields by the reaction of (S)-(+)-1,2,3,4-tetrahydro-1-naphthylamine/(R)-(-)-1,2,3,4-tetrahydro-1-naphthylamine with various 4-substitutedbenzoyl chlorides in diethylether at room temperature. All reactions have been monitored by Thin Layer Chromatography (TLC). Structures of all synthesized compunds have been illuminated not only by physical and chemical methods and also spectroscopic methods such as UV-Vis, FT IR, 1H NMR, 13C NMR, MS and Elemental Analysis (C, H, N, S) technique.en_US
dc.languageTurkish
dc.language.isotr
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAttribution 4.0 United Statestr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectKimyatr_TR
dc.subjectChemistryen_US
dc.title1,2,3,4-tetrahidro-1-naftilamin`in enantiyomerlerinden türeyen kiral amitlerin sentezi ve yapılarının karakterizasyonu
dc.title.alternativeSynthesis and characterization of chiral amides derived from enantiomers of 1,2,3,4-tetrahydro-1-naphtylamine
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentKimya Anabilim Dalı
dc.identifier.yokid10063194
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityGAZİANTEP ÜNİVERSİTESİ
dc.identifier.thesisid382639
dc.description.pages128
dc.publisher.disciplineDiğer


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