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

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.identifier.isbn	978-80-7395-814-5
dc.identifier.issn	1211-5541
dc.identifier.uri	https://hdl.handle.net/10195/75421
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.language.iso	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
dc.peerreviewed	yes	en
dc.publicationstatus	published	en