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dc.contributor.advisorŞendil, Kıvılcım
dc.contributor.authorOğuz, Mehmet
dc.date.accessioned2020-12-06T10:01:40Z
dc.date.available2020-12-06T10:01:40Z
dc.date.submitted2014
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/96927
dc.description.abstractBu tez çalışmasında ilk olarak, 5,5′-metilen-bis-salisilaldehit bileşiği, salisilaldehit ile trioksanın uygun ortamda reaksiyonundan literatüre göre elde edilmiştir. Çalışmanın diğer basamağında ise 5,5′-metilen-bis-salisilaldehit ile 3 kiral optikçe aktif bileşiğin (L-valin, alanin, metiyonin) reaksiyonlarından optikçe aktif 3 yeni Schiff bazı (5,5′-metilen-bis-salisiliden-amino-etil-3-metil butanoikasit, 5,5'-metilen-bis-salisiliden-amino-etil-aspartik asit ve 5,5′-metilen-bis-salisiliden-amino-etil-3-metil propanoikasit bileşikleri sentezlenmiş, 1H-NMR ve 13C-NMR spektrumları yorumlanmıştır.
dc.description.abstractIn this thesis, first the 5,5′-methylene-bis-salicylaldehyde compound has been synthesized by the reaction of salicylaldehyde with trioxane under proper condition according to the literature. The structure of 5,5′-methylene-bis-salicylaldehyde has been completely enlightened 1H-NMR and 13C-NMR analysis. In the next stage of the study, 3 optically active new Schiff bases (5,5′-methylene-bis-salicylidene-amino-ethyl-3-methyl butanoic acid, 5,5′-methylene-bis-salicylidene-amino-ethyl-aspartic acid and 5,5′-methylene-bis-salicylidene-amino-ethyl-3-methyl propanoic acid) have been synthesized from the reaction of 3 optically active (L-valine, aspartic acid and L-alanine) 1H-NMR and 13C-NMR spectrum of these compounds have been collected and interpreted.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.titleUltrasonik şartlarda yeni bir yöntem ile kiral amino asitlerden kiral iminlerin sentezi
dc.title.alternativeSynthesis of chiral imines from chiral amino acids with a new method under ultrasonic conditions
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentKimya Anabilim Dalı
dc.identifier.yokid10040209
dc.publisher.instituteFen Bilimleri Enstitüsü
dc.publisher.universityKAFKAS ÜNİVERSİTESİ
dc.identifier.thesisid374089
dc.description.pages64
dc.publisher.disciplineDiğer


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