Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19756
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2022-06-22T08:10:47Z-
dc.date.available2022-06-22T08:10:47Z-
dc.date.issued2022-
dc.identifier.citationKolodina, A. A., Steglenko, D. V., Khodykina, E. S., Gaponenko, N. I., Galkina, M. S., Demidov, O. P., Metelitsa, A. V. Unusual cyclization of N-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclization // Mendeleev Communications. - 2022. - Том 32. - Выпуск 3. - Стр.: 386 - 389. - DOI10.1016/j.mencom.2022.05.032ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19756-
dc.description.abstract2,6-Di-tert-butyl-4-{[2-(2-aryl-2-oxoethylthio)-1H-imidazol-1-yl]imino}cyclohexa-2,5-dien-1-ones under the action of bases give products of the 2,3-dihydroimidazo[2,1-b]thiazol- 3-ol series by subsequent recyclization reaction of the intermediate imidazo[2,1-b][1,3,4]thiadiazoles. The structure of imidazo[2,1-b]thiazol-3-ol is supported by the X-ray diffraction. The features of the cyclization processes of quinone imine derivatives were stimulated by DFT calculations using the wB97XD/6-311++G** method.ru
dc.language.isoenru
dc.publisherElsevier Ltdru
dc.relation.ispartofseriesMendeleev Communications-
dc.subjectDFT calculationsru
dc.subjectImidazo[2,1-b]thiazolesru
dc.subjectImidazo[2,1-b][1,3,4]thiadiazolesru
dc.subjectN-hetaryl quinone iminesru
dc.subjectRecyclizationru
dc.titleUnusual cyclization of N-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclizationru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File SizeFormat 
scopusresults 2229 .pdf
  Restricted Access
389.43 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.