| 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 |