Recyclizations of 2-aminobenzylimines and thioaroylhydrazones of N-substituted N-hydroxy-3-oxobutanamides

dc.contributor.author	Zelenin K.
dc.contributor.author	Lagoda I.
dc.contributor.author	Alekseyev V.
dc.contributor.author	Sinkkonen J.
dc.contributor.author	Shaikhutdinov R.
dc.contributor.author	Pihlaja K.
dc.date.accessioned	2018-09-17T20:22:05Z
dc.date.available	2018-09-17T20:22:05Z
dc.date.issued	2002
dc.identifier.issn	0022-152X
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/133406
dc.description.abstract	A universal scheme is proposed for the molecular design of heterocyclic recyclizations by replacing the exocyclic hydroxyl groups in exo-trig- ring-chain tautomeric molecules with substituted amines or hydrazines. The practical applicability of this approach is demonstrated by the condensations of 5-hydroxy-5-methyl-3-isoxazolidinones with thioaroyl-hydrazines and 2-aminomethylaniline. The condensation products were studied by modern 1H, 13C and 15N NMR spectroscopic methods using three solvents: CDCl3, DMSO[D6] and CD3CN. The solvent was found to have a strong effect to the relative amounts of the tautomers.
dc.relation.ispartofseries	Journal of Heterocyclic Chemistry
dc.title	Recyclizations of 2-aminobenzylimines and thioaroylhydrazones of N-substituted N-hydroxy-3-oxobutanamides
dc.type	Article
dc.relation.ispartofseries-issue	4
dc.relation.ispartofseries-volume	39
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	805
dc.source.id	SCOPUS0022152X-2002-39-4-SID0036666329

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Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.