Some observations concerning the tautomerization of γ-keto amides Schiff bases to 2-aminopyrrolidin-5-ones

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	2014-03-01T01:55:28Z
dc.date.available	2014-03-01T01:55:28Z
dc.date.issued	2006	en
dc.identifier.issn	07930283	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/27750
dc.relation.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-33751244225&partnerID=40&md5=3b267aeacac860b6471b3ac7cad1fd8f	en
dc.subject	2-Aminopyrrolidin-5-ones	en
dc.subject	4-Oxo-5-phenylpentanamides	en
dc.subject	4-Oxo-pentanamides	en
dc.subject	Tautomerism of γ-keto amides Schiff bases	en
dc.title	Some observations concerning the tautomerization of γ-keto amides Schiff bases to 2-aminopyrrolidin-5-ones	en
heal.type	journalArticle	en
heal.publicationDate	2006	en
heal.abstract	The reactions of excess of primary amines, with the anhydride or the lactone, (γ-benzylidene-γ-butyrolactone), of 4-oxo-5-phenylpentanoic acid or with its amides, and with α-angelicalactone and 4-oxopentanoic acid amides, resulted to the corresponding 2-aminopyrrolidin-5-ones, the cyclic tautomers of the Schiff bases of γ-keto amides.	en
heal.journalName	Heterocyclic Communications	en
dc.identifier.volume	12	en
dc.identifier.issue	6	en
dc.identifier.spage	419	en
dc.identifier.epage	422	en