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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 |