Reactions of S-, N-ambident nucleophiles with polarized ethylenes giving pyrimidines and 1,3-thiazines

Publikace:
Reactions of S-, N-ambident nucleophiles with polarized ethylenes giving pyrimidines and 1,3-thiazines

Článekopen accesspeer-reviewedpublished

dc.contributor.author	Tarabová, Denisa
dc.contributor.author	Hanusek, Jiří
dc.date.accessioned	2020-05-18T18:27:08Z
dc.date.available	2020-05-18T18:27:08Z
dc.date.issued	2014
dc.description.abstract	The review is focused on a diverse use of polarized ethylenes bearing an alkoxy, halogen or amino group in the reaction with S-, N- ambident nucleophiles (thioamides, thioureas, thiosemicarbazides, thiocarbamates, dithiocarbamates) to give pyrimidine and 1,3-thiazine ring. Other possibilities of synthesis of these heterocyclic scaffolds are also reported.	en
dc.format	p. 229–247
dc.identifier.isbn	978-80-7395-814-5
dc.identifier.issn	1211-5541
dc.identifier.uri	https://hdl.handle.net/10195/75421
dc.language.iso	en
dc.peerreviewed	yes	en
dc.publicationstatus	published	en
dc.publisher	University of Pardubice	en
dc.relation.ispartof	Scientific papers of the University of Pardubice. Series A, Faculty of Chemical Technology. 20/2014	en
dc.rights	open access	en
dc.title	Reactions of S-, N-ambident nucleophiles with polarized ethylenes giving pyrimidines and 1,3-thiazines	en
dc.type	Article	en
dspace.entity.type	Publication

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