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Synthesis of new 5-alkyl substituted 4-thiazolidinones utilising condensation with ethyl 2-bromo alkanoates

dc.contributor.authorKlip, Nalan Terzioglu
dc.contributor.authorGuezel, Oezlen
dc.contributor.authorGuersoy, Aysel
dc.date.accessioned2021-03-05T21:53:49Z
dc.date.available2021-03-05T21:53:49Z
dc.date.issued2008
dc.identifier.citationKlip N. T. , Guezel O., Guersoy A., "Synthesis of new 5-alkyl substituted 4-thiazolidinones utilising condensation with ethyl 2-bromo alkanoates", JOURNAL OF CHEMICAL RESEARCH, ss.378-379, 2008
dc.identifier.issn1747-5198
dc.identifier.otherav_db1b92c7-2f17-4d06-a055-51ac5af720fd
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/144419
dc.identifier.urihttps://doi.org/10.3184/030823408x332194
dc.description.abstract2-[(3-Ethyl-4-oxo-3,4-dihydroquinazolin-2-yl)mercaptoacetyl hydrazono]-3-alkyl/aralkyl-5-ethyl/propylthiazolidin-4-ones were synthesised by the cyclisation of 1-[(3-ethyl-4-oxo-3,4-dihydroquinazolin-2-yl)mercaptoacetyl]-4alkyl/aralkyl thiosemicarbazides with ethyl 2-bromobutanoate or ethyl 2-bromopentanoate in the presence of anhydrous sodium acetate in anhydrous ethanolic medium. The regioisomer 2-alkyl/aralkyl 3-[(3-ethyl-4-oxo-3,4dihydroquinazolin-2-yl)mercaptoacetylamino]-5-ethyl/propylthiazolidin-4-ones were not formed.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectTemel Bilimler
dc.subjectAlkoloidler
dc.subjectKİMYA, MULTİDİSİPLİNER
dc.subjectBiyokimya
dc.subjectKimya
dc.titleSynthesis of new 5-alkyl substituted 4-thiazolidinones utilising condensation with ethyl 2-bromo alkanoates
dc.typeMakale
dc.relation.journalJOURNAL OF CHEMICAL RESEARCH
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.issue7
dc.identifier.startpage378
dc.identifier.endpage379
dc.contributor.firstauthorID188477


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