Regioselective reduction of 5-substituted 2-alkylidene-4-oxothiazolidines by metal hydrides

dc.creator	Marković, R.
dc.creator	Baranac-Stojanović, Marija
dc.creator	Stojanović, Milovan
dc.date.accessioned	2018-11-22T00:06:58Z
dc.date.available	2018-11-22T00:06:58Z
dc.date.issued	2004
dc.identifier.issn	0936-5214
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/637
dc.description.abstract	Thiazolidine beta-enamino derivatives possessing a 5-substituted acetate substituent were chemoselectively reduced to corresponding alcohols, or new condensed 2-alkylidenethiazolidines. The method is based on the resistance of an enaminone fragment to reduction by metal hydrides.	en
dc.publisher	Georg Thieme Verlag Kg, Stuttgart
dc.rights	restrictedAccess
dc.source	Synlett
dc.subject	thiazolidine	en
dc.subject	reductions	en
dc.subject	hydrides	en
dc.subject	regioselectivity	en
dc.subject	ring closure	en
dc.title	Regioselective reduction of 5-substituted 2-alkylidene-4-oxothiazolidines by metal hydrides	en
dc.type	article
dc.rights.license	ARR
dcterms.abstract	Марковиц, Р; Стојановиц, М; Баранац-Стојановић, Марија;
dc.citation.issue	6
dc.citation.spage	1034
dc.citation.epage	1038
dc.identifier.wos	000221385700025
dc.identifier.doi	10.1055/s-2004-820051
dc.citation.other	(6): 1034-1038
dc.citation.rank	M21
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-3142751084

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