| dc.contributor.author |
Couladouros, EA |
en |
| dc.contributor.author |
Plyta, ZF |
en |
| dc.contributor.author |
Iliadis, T |
en |
| dc.contributor.author |
Roussis, V |
en |
| dc.contributor.author |
Papageorgiou, VP |
en |
| dc.date.accessioned |
2014-06-06T06:43:11Z |
|
| dc.date.available |
2014-06-06T06:43:11Z |
|
| dc.date.issued |
1996 |
en |
| dc.identifier.issn |
0022152X |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1068 |
|
| dc.relation.uri |
http://www.scopus.com/inward/record.url?eid=2-s2.0-0001409124&partnerID=40&md5=5a19ed231b330e97fe1e233f0aaf3012 |
en |
| dc.title |
Heteroannulation of naphthoquinones. Studies on the reaction of 2-bromo-2,3-dihydronaphthoquinone derivatives with 1,2-binucleophiles |
en |
| heal.type |
journalArticle |
en |
| heal.publicationDate |
1996 |
en |
| heal.abstract |
Heterocyclic derivatives of naphthoquinones were synthesized via their 2-bromo-2,3-dehydro-intermediates. This new route may lead to the formation of benzo[a]phenothiazin-5-ones, benzo[f]quinoxalin-6-ones as well as their 1,4 (or 7,10) dihydroxy-derivatives in high yields. The possible mechanisms involved in the formation of these compounds are discussed. |
en |
| heal.journalName |
Journal of Heterocyclic Chemistry |
en |
| dc.identifier.issue |
3 |
en |
| dc.identifier.volume |
33 |
en |
| dc.identifier.spage |
709 |
en |
| dc.identifier.epage |
714 |
en |