dc.contributor.author |
Tsolomiti, G |
en |
dc.contributor.author |
Tsolomiti, K |
en |
dc.contributor.author |
Tsolomitis, A |
en |
dc.date.accessioned |
2014-03-01T01:27:46Z |
|
dc.date.available |
2014-03-01T01:27:46Z |
|
dc.date.issued |
2008 |
en |
dc.identifier.issn |
0793-0283 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/18562 |
|
dc.relation.uri |
http://www.scopus.com/inward/record.url?eid=2-s2.0-43749108144&partnerID=40&md5=fbf88bfcacb41d296e767c725a22e155 |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
ANTAGONISTS |
en |
dc.subject.other |
QUINONES |
en |
dc.subject.other |
DESIGN |
en |
dc.title |
A new method for synthesizing 1H-1-benzazepine-2,5-dione derivatives from n,n-substituted maleamic acids |
en |
heal.type |
journalArticle |
en |
heal.language |
English |
en |
heal.publicationDate |
2008 |
en |
heal.abstract |
N,N-Substituted maleamic acids have been found to be converted, via the corresponding acid chlorides, through an intramolecular Friedel-Crafts reaction to 1H-1-benzazepine-2,5-dione derivatives in good overall yields. |
en |
heal.publisher |
FREUND PUBLISHING HOUSE LTD |
en |
heal.journalName |
Heterocyclic Communications |
en |
dc.identifier.isi |
ISI:000260108100014 |
en |
dc.identifier.volume |
14 |
en |
dc.identifier.issue |
1-2 |
en |
dc.identifier.spage |
89 |
en |
dc.identifier.epage |
94 |
en |