An unexpected synthesis of 1,5,5-trisubstituted 3,4-dibromo-3-pyrrolin-2- ones from an open-chain tautomer γ-ketoamide

Tsolomiti, G; Tsolomiti, K; Tsolomitis, A

dc.contributor.author	Tsolomiti, G	en
dc.contributor.author	Tsolomiti, K	en
dc.contributor.author	Tsolomitis, A	en
dc.date.accessioned	2014-03-01T01:23:35Z
dc.date.available	2014-03-01T01:23:35Z
dc.date.issued	2006	en
dc.identifier.issn	0793-0283	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/17036
dc.relation.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-33751253443&partnerID=40&md5=1d092f715c2a9c672771d8ec3bc7ba55	en
dc.subject.classification	Chemistry, Organic	en
dc.subject.other	AMIDES	en
dc.subject.other	ACID	en
dc.title	An unexpected synthesis of 1,5,5-trisubstituted 3,4-dibromo-3-pyrrolin-2- ones from an open-chain tautomer γ-ketoamide	en
heal.type	journalArticle	en
heal.language	English	en
heal.publicationDate	2006	en
heal.abstract	The unexpected synthesis of 1,5,5-trisubstituted 3,4-dibromo-3-pyrrolin-2- ones 6, from the reaction of the 1-benzyl-5-phenyl-3,4,5-tribromo-3-pyrrolin-2- one 5, resulting from the reaction of 3-benzoylpropionamide 1 using a threefold excess of bromine, with different nucleophiles, is described.	en
heal.publisher	FREUND PUBLISHING HOUSE LTD	en
heal.journalName	Heterocyclic Communications	en
dc.identifier.isi	ISI:000241956200011	en
dc.identifier.volume	12	en
dc.identifier.issue	5	en
dc.identifier.spage	365	en
dc.identifier.epage	368	en