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

Please use this identifier to cite or link to this item: https://dspace.bsmu.edu.ua/handle/123456789/9031

Full metadata record

DC Field	Value	Language
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	https://dspace.bsmu.edu.ua/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
Appears in Collections:	Статті. Кафедра фармації

Files in This Item:

File	Description	Size	Format
СТАТТЯ.pdf		210.3 kB	Adobe PDF	View/Open

DSpace JSPUI