Please use this identifier to cite or link to this item: http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/9031
Title: Polyfunctional Imidazoles: VIII.* 1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazoles
Authors: Grozav, A.N.
Chornous, V.A.
Palamar, A.A.
Vovk, M.V.
Keywords: 1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazoles
propargyl bromide,
chloroacetic acid
Issue Date: 2014
Publisher: RUSSIAN JOURNAL OF ORGANIC CHEMISTRY Vol. 50 No. 9 2014
Abstract: Alkylation 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.
URI: http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/9031
ISBN: DOI:10.1134/S1070428014090164
Appears in Collections:Статті. Кафедра фармації

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