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dc.contributor.authorKutuk, H
dc.contributor.authorBekdemir, Y
dc.contributor.authorTurkoz, N
dc.date.accessioned2020-06-21T15:28:59Z
dc.date.available2020-06-21T15:28:59Z
dc.date.issued2006
dc.identifier.issn1042-6507
dc.identifier.urihttps://doi.org/10.1080/10426500500272186
dc.identifier.urihttps://hdl.handle.net/20.500.12712/20676
dc.descriptionWOS: 000236358600022en_US
dc.description.abstractThe acid-catalyzed hydrolysis of 2-oxo-3-(p-substituted)-phenyl-5-methyl-1,2,3-oxathiazolidines (1) have been studied in 60% (v/v) 1,4 dioxane-aqueous solutions of perchloric and hydrochloric acids at 10.0 +/- 0.05 degrees C. The analysis of the kinetic data by the order of the catalytic effects of the acids, activation parameters, kinetic solvent isotope effect, and substituent effect are all in agreement with an A-2 mechanism in the studied range.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.1080/10426500500272186en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectacid-catalyzed hydrolysisen_US
dc.subjectamidosulfitesen_US
dc.subjectoxathiazolidinesen_US
dc.subjectsubstituent effecten_US
dc.titleThe synthesis and substituent effect of the acid catalyzed hydrolysis of amidosulfitesen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume181en_US
dc.identifier.issue4en_US
dc.identifier.startpage931en_US
dc.identifier.endpage937en_US
dc.relation.journalPhosphorus Sulfur and Silicon and the Related Elementsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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