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1,4-Reductive addition of hydrazoic acid to γ-oxo-α,β-unsaturated δ- lactones and -lactams: A convenient route to α-amino-γ-oxo-α,β- unsaturated δ-lactones and -lactams

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dc.contributor.author Koulocheri, SD en
dc.contributor.author Haroutounian, SA en
dc.contributor.author Apostolopoulos, CD en
dc.contributor.author Chada, RK en
dc.contributor.author Couladouros, EA en
dc.date.accessioned 2014-06-06T06:44:00Z
dc.date.available 2014-06-06T06:44:00Z
dc.date.issued 1999 en
dc.identifier.issn 1434193X en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/1620
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0032795214&partnerID=40&md5=b4c345d0361af7278efcf891b1193b80 en
dc.subject δ-Lactams en
dc.subject δ-Lactones en
dc.subject Hydrazoic acid en
dc.subject Oxo enamines en
dc.subject Reductive addition en
dc.subject.other hydrazone derivative en
dc.subject.other lactam derivative en
dc.subject.other lactone derivative en
dc.subject.other article en
dc.subject.other chemical reaction en
dc.subject.other chemical structure en
dc.subject.other reaction analysis en
dc.subject.other reduction en
dc.subject.other synthesis en
dc.title 1,4-Reductive addition of hydrazoic acid to γ-oxo-α,β-unsaturated δ- lactones and -lactams: A convenient route to α-amino-γ-oxo-α,β- unsaturated δ-lactones and -lactams en
heal.type journalArticle en
heal.publicationDate 1999 en
heal.abstract γ-Oxo-α,β-unsaturated δ-lactones and lactams, which are easily accessible from their corresponding 2-furylcarbinols, were used as substrates for the 1,4-reductive addition of hydrazoic acid. The outcome of the reaction is the formation, in high yields, of the corresponding α-amino-γ-oxo-α,β- unsaturated δ-lactones and -lactams, compounds of great biological and synthetic interest. en
heal.journalName European Journal of Organic Chemistry en
dc.identifier.issue 6 en
dc.identifier.spage 1449 en
dc.identifier.epage 1453 en


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