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First example of the synthesis of S,O-macroheterocycle based on 2(5H)-furanone and 2,2´-oxydiethanethiol

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dc.contributor.author Kurbangalieva A.
dc.contributor.author Hoang L.
dc.contributor.author Lodochnikova O.
dc.contributor.author Kuzmicheva M.
dc.contributor.author Pradipta A.
dc.contributor.author Tanaka K.
dc.contributor.author Chmutova G.
dc.date.accessioned 2018-09-19T20:56:47Z
dc.date.available 2018-09-19T20:56:47Z
dc.date.issued 2016
dc.identifier.issn 1066-5285
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/143453
dc.description.abstract © 2016, Springer Science+Business Media New York.A base-catalyzed reaction of 3,4-dichloro-5-methoxy- and 3,4-dichloro-5-ethoxy-2(5H)-furanones with 2,2´-oxydiethanethiol gave thiols and bis-thioethers of 2(5H)-furanone series. A new S,O-macroheterocyclic compound containing a 18-membered oxathiamacrocycle and two 2(5H)-furanone fragments was synthesized based on the thiols in an aqueous solution of potassium hydroxide, which was characterized by X-ray diffraction.
dc.relation.ispartofseries Russian Chemical Bulletin
dc.subject 2(5H)-furanones
dc.subject 2,2´-oxydiethanethiol
dc.subject bis-thioethers
dc.subject lactones
dc.subject macrocyclization
dc.subject macroheterocycles
dc.subject single crystal X-ray diffraction
dc.subject thiilation
dc.subject thiols
dc.title First example of the synthesis of S,O-macroheterocycle based on 2(5H)-furanone and 2,2´-oxydiethanethiol
dc.type Article
dc.relation.ispartofseries-issue 5
dc.relation.ispartofseries-volume 65
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 1278
dc.source.id SCOPUS10665285-2016-65-5-SID85010635745


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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