Polyfunctional Imidazoles: VIII.* 1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazoles

Grozav, A.N.; Chornous, V.A.; Palamar, A.A.; Vovk, M.V.

dc.contributor.author	Grozav, A.N.
dc.contributor.author	Chornous, V.A.
dc.contributor.author	Palamar, A.A.
dc.contributor.author	Vovk, M.V.
dc.date.accessioned	2015-06-09T08:12:44Z
dc.date.available	2015-06-09T08:12:44Z
dc.date.issued	2014
dc.identifier.isbn	DOI:10.1134/S1070428014090164
dc.identifier.uri	http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/9031
dc.description.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.	ru_RU
dc.description.sponsorship	Кафедра фармації	ru_RU
dc.language.iso	other	ru_RU
dc.publisher	RUSSIAN JOURNAL OF ORGANIC CHEMISTRY Vol. 50 No. 9 2014	ru_RU
dc.subject	1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazoles	ru_RU
dc.subject	propargyl bromide,	ru_RU
dc.subject	chloroacetic acid	ru_RU
dc.title	Polyfunctional Imidazoles: VIII.* 1-Aryl-4-chloro- 5-[R-sulfanyl(R-sulfonyl)methyl]-1H-imidazoles	ru_RU
dc.type	Other	ru_RU