| dc.contributor.author |
Couladouros, EA |
en |
| dc.contributor.author |
Plyta, ZF |
en |
| dc.contributor.author |
Papageorgiou, VP |
en |
| dc.date.accessioned |
2014-06-06T06:43:09Z |
|
| dc.date.available |
2014-06-06T06:43:09Z |
|
| dc.date.issued |
1996 |
en |
| dc.identifier.issn |
00223263 |
en |
| dc.identifier.uri |
http://dx.doi.org/10.1021/jo9517252 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1041 |
|
| dc.subject.other |
14 naphthoquinone derivative |
en |
| dc.subject.other |
naphthazacin derivative |
en |
| dc.subject.other |
unclassified drug |
en |
| dc.subject.other |
article |
en |
| dc.subject.other |
drug synthesis |
en |
| dc.subject.other |
reaction analysis |
en |
| dc.subject.other |
technique |
en |
| dc.title |
A general procedure for the efficient synthesis of (alkylamino)naphthoquinones |
en |
| heal.type |
journalArticle |
en |
| heal.identifier.primary |
10.1021/jo9517252 |
en |
| heal.publicationDate |
1996 |
en |
| heal.abstract |
Alkylamino derivatives of naphthazarine, juglone, and naphthoquinone have been synthesized via their corresponding bromo-analogues, in high yields, especially in the case of naphthazarins. |
en |
| heal.journalName |
Journal of Organic Chemistry |
en |
| dc.identifier.issue |
9 |
en |
| dc.identifier.volume |
61 |
en |
| dc.identifier.doi |
10.1021/jo9517252 |
en |
| dc.identifier.spage |
3031 |
en |
| dc.identifier.epage |
3033 |
en |