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dc.contributor.authorGrozav, A.N.-
dc.contributor.authorChornous, V.A.-
dc.contributor.authorPalamar, A.A.-
dc.contributor.authorVovk, M.V.-
dc.date.accessioned2015-06-09T08:12:44Z-
dc.date.available2015-06-09T08:12:44Z-
dc.date.issued2014-
dc.identifier.isbnDOI:10.1134/S1070428014090164-
dc.identifier.urihttp://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/9031-
dc.description.abstractAlkylation of (1-aryl-4-chloro-1H-imidazol-5-yl)methanethiols with alkyl halides, propargyl bromide, or chloroacetic acid gave 1-aryl-5-(R-sulfanylmethyl)-4-chloro-1H-imidazoles. 1-Aryl-4-chloro-5-(methylsulfanylmethyl)-1H-imidazoles and [(1-aryl-4-chloro-1H-imidazol-5-yl)methylsulfanyl]acetic acids were oxidized to the corresponding sulfones with potassium permanganate.ru_RU
dc.description.sponsorshipКафедра фармаціїru_RU
dc.language.isootherru_RU
dc.publisherRUSSIAN JOURNAL OF ORGANIC CHEMISTRY Vol. 50 No. 9 2014ru_RU
dc.subject1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazolesru_RU
dc.subjectpropargyl bromide,ru_RU
dc.subjectchloroacetic acidru_RU
dc.titlePolyfunctional Imidazoles: VIII.* 1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazolesru_RU
dc.typeOtherru_RU
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