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dc.contributor.authorOzkirimli, Sumru
dc.contributor.authorDemir-Dundar, Hale
dc.contributor.authorDEMİR ORDU, ÖZNUR
dc.date.accessioned2021-03-05T19:11:54Z
dc.date.available2021-03-05T19:11:54Z
dc.identifier.citationDEMİR ORDU Ö., Demir-Dundar H., Ozkirimli S., "Stereochemical Investigations of Diastereomeric N-[2-(Aryl)-5-methyl-4-oxo-1,3-thiazolidine-3-yl]-pyridine-3-carboxamides by Nuclear Magnetic Resonance Spectroscopy (1D and 2D)", INTERNATIONAL JOURNAL OF SPECTROSCOPY, 2015
dc.identifier.othervv_1032021
dc.identifier.otherav_ce25eeef-5c47-4bbe-842b-f4ec782c143d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/136375
dc.identifier.urihttps://doi.org/10.1155/2015/609250
dc.description.abstractSome new N-[2-(aryl)-5-methyl-4-oxo-1,3-thiazolidine-3-yl]-pyridine-3-carboxamides were synthesized and their structures were investigated by IR, NMR(H-1, C-13, and 2D), and mass spectra. The presence of C-2 and C-5 stereogenic centers on the thiazolidinone ring resulted in diastereoisomeric pairs. The configurations of two stereogenic centers were assigned based upon H-1 NMR analysis of coupling constants and 2D nuclear overhauser enhancement spectroscopy (NOESY) experiment. Resolution of the diastereoisomers was performed by high performance liquid chromatography (HPLC) using a chiral stationary phase.
dc.language.isoeng
dc.subjectSpektroskopi
dc.subjectTemel Bilimler
dc.subjectFizikokimya
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectSPEKTROSKOPİ
dc.titleStereochemical Investigations of Diastereomeric N-[2-(Aryl)-5-methyl-4-oxo-1,3-thiazolidine-3-yl]-pyridine-3-carboxamides by Nuclear Magnetic Resonance Spectroscopy (1D and 2D)
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF SPECTROSCOPY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.contributor.firstauthorID219583


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