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dc.contributor.authorYusufoglu, Ayşe Sergüzel
dc.contributor.authorKucuk, Hatice Baspinar
dc.date.accessioned2021-03-04T17:50:11Z
dc.date.available2021-03-04T17:50:11Z
dc.date.issued2012
dc.identifier.citationKucuk H. B. , Yusufoglu A. S. , "Synthesis of New Chiral and Racemic 1,3-Dioxolanes", JOURNAL OF HETEROCYCLIC CHEMISTRY, cilt.49, ss.1066-1070, 2012
dc.identifier.issn0022-152X
dc.identifier.otherav_877ac970-9316-48d6-b5b3-43c04ec17c33
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/92039
dc.identifier.urihttps://doi.org/10.1002/jhet.937
dc.description.abstractA series of chiral 1,3-dioxolanes, 3-12, with > 99% ee values, have been synthesized. This is the first study of chiral ketalization reaction starting from ketones with aryl, monosubstituted aryl, and long alkyl chains (C-11-AC(13)). Their ee values were determined by chiral high-performance liquid chromatography (HPLC) on Chiralcel OD column, using their racemic 1,3-dioxolanes rac-3-12, which were also synthesized for the first time. These chiral and racemic 1,3-dioxolanes were characterizated by infrared, NMR (H-1, C-13), mass spectrometry, elemental analysis, optical rotation, and chiral HPLC.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectBiyoinorganik Kimya
dc.subjectKİMYA, ORGANİK
dc.subjectKimya
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.titleSynthesis of New Chiral and Racemic 1,3-Dioxolanes
dc.typeMakale
dc.relation.journalJOURNAL OF HETEROCYCLIC CHEMISTRY
dc.contributor.departmentİstanbul Üniversitesi , Mühendislik Fakültesi , Kimya
dc.identifier.volume49
dc.identifier.issue5
dc.identifier.startpage1066
dc.identifier.endpage1070
dc.contributor.firstauthorID6508


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