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 |
2014-06-06T06:43:49Z |
|
dc.date.available |
2014-06-06T06:43:49Z |
|
dc.date.issued |
1999 |
en |
dc.identifier.issn |
1434-193X |
en |
dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1480 |
|
dc.subject |
oxo enamines |
en |
dc.subject |
reductive addition |
en |
dc.subject |
hydrazoic acid |
en |
dc.subject |
delta-lactones |
en |
dc.subject |
delta-lactams |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
ALPHA-FURFURYL AMIDE |
en |
dc.subject.other |
EFFICIENT PREPARATION |
en |
dc.subject.other |
AMINES |
en |
dc.subject.other |
TRANSFORMATION |
en |
dc.subject.other |
DERIVATIVES |
en |
dc.subject.other |
PRODUCTS |
en |
dc.subject.other |
ANALOGS |
en |
dc.subject.other |
FURANS |
en |
dc.title |
1,4-reductive addition of hydrazoic acid to gamma-oxo-alpha,beta-unsaturated delta-lactones and -lactams: A convenient route to alpha-amino-gamma-oxo-alpha,beta-unsaturated delta-lactones and -lactams |
en |
heal.type |
journalArticle |
en |
heal.language |
English |
en |
heal.publicationDate |
1999 |
en |
heal.abstract |
gamma-Oxo-alpha,beta-unsaturated delta-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 alpha-amino-gamma-oxo-alpha,beta-unsaturated delta-lactones and -lactams, compounds of great biological and synthetic interest. |
en |
heal.publisher |
WILEY-V C H VERLAG GMBH |
en |
heal.journalName |
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY |
en |
dc.identifier.issue |
6 |
en |
dc.identifier.isi |
ISI:000080738500022 |
en |
dc.identifier.spage |
1449 |
en |
dc.identifier.epage |
1453 |
en |