Six-membered cyclic semiaminal as intermediate in the synthesis of thiazoles from thiosemicarhazide and α-haloketones

dc.contributor.author	Mamedov V.
dc.contributor.author	Berdnikov E.
dc.contributor.author	Valeeva V.
dc.contributor.author	Ismaev I.
dc.contributor.author	Rizvanov I.
dc.contributor.author	Antokhina L.
dc.contributor.author	Nuretdinov I.
dc.contributor.author	Chernov P.
dc.date.accessioned	2018-09-17T21:16:50Z
dc.date.available	2018-09-17T21:16:50Z
dc.date.issued	1993
dc.identifier.issn	1066-5285
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/134776
dc.description.abstract	Cyclization of thiosemicarbazide with methyl 3-chloro-2-oxo-3-phenylpropionate in MeCN results in 5-hydroxy-2-imino-5-methoxycarbonyl-6-phenylperhydro-1,3,4-thiadiazine. The structure of the product has been confirmed using spectral (IR,1H,13C,13C{1H} NMR) methods and chemical transformations. © 1994 Plenum Publishing Corporation.
dc.relation.ispartofseries	Russian Chemical Bulletin
dc.subject	2-amino-and 2-hydrazinothiazoles
dc.subject	cyclic hemiaminals
dc.subject	thiadiazine
dc.title	Six-membered cyclic semiaminal as intermediate in the synthesis of thiazoles from thiosemicarhazide and α-haloketones
dc.type	Article
dc.relation.ispartofseries-issue	11
dc.relation.ispartofseries-volume	42
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	1879
dc.source.id	SCOPUS10665285-1993-42-11-SID25444440955

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