Catalytic oxidations of enolizable ketones using 2-alkylidene-4- oxothiazolidine vinyl bromide

dc.creator	Baranac-Stojanović, Marija
dc.creator	Marković, Rade
dc.creator	Stojanović, Milovan
dc.date.accessioned	2019-01-30T17:28:59Z
dc.date.available	2019-01-30T17:28:59Z
dc.date.issued	2011
dc.identifier.issn	0040-4020
dc.identifier.uri	https://cer.ihtm.bg.ac.rs/handle/123456789/936
dc.description.abstract	Direct oxidation of enolizable ketones to α-hydroxy derivatives, vicinal dicarbonyls or tricarbonyl compounds has been achieved by a catalytic amount of 2-alkylidene-4-oxothiazolidine vinyl bromide in DMSO as a solvent. The yields range from moderate to good.	en
dc.publisher	Oxford : Pergamon-Elsevier Science Ltd
dc.relation	info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.rights	restrictedAccess
dc.source	Tetrahedron
dc.subject	2-Alkylidene-4-oxothiazolidine vinyl bromide	en
dc.subject	Catalytic oxidation	en
dc.subject	Dimethyl sulfoxide	en
dc.subject	Enolizable ketones	en
dc.title	Catalytic oxidations of enolizable ketones using 2-alkylidene-4- oxothiazolidine vinyl bromide	en
dc.type	article
dc.rights.license	ARR
dcterms.abstract	Марковић, Р.; Стојановић, Милован; Баранац-Стојановић, М.;
dc.citation.volume	67
dc.citation.issue	41
dc.citation.spage	8000
dc.citation.epage	8008
dc.citation.other	67(41): 8000-8008
dc.citation.rank	M21
dc.identifier.doi	10.1016/j.tet.2011.08.022
dc.identifier.scopus	2-s2.0-80052769356
dc.identifier.wos	000295564100016
dc.type.version	publishedVersion