dc.contributor.author |
Couladouros, EA |
en |
dc.contributor.author |
Strongilos, AT |
en |
dc.date.accessioned |
2014-06-06T06:44:23Z |
|
dc.date.available |
2014-06-06T06:44:23Z |
|
dc.date.issued |
2000 |
en |
dc.identifier.issn |
0040-4039 |
en |
dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1854 |
|
dc.subject |
juglone derivatives |
en |
dc.subject |
oxidation |
en |
dc.subject |
salcomine |
en |
dc.subject |
[bis(trifluoroacetoxy)iodo]benzene |
en |
dc.subject |
naphthoquinones |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
EFFICIENT SYNTHESIS |
en |
dc.subject.other |
CALPHOSTIN-A |
en |
dc.subject.other |
NAPHTHOQUINONES |
en |
dc.subject.other |
PHLEICHROME |
en |
dc.title |
Regioselective oxidation of 3-monosubstituted juglone derivatives |
en |
heal.type |
journalArticle |
en |
heal.language |
English |
en |
heal.publicationDate |
2000 |
en |
heal.abstract |
Derivatives of 3-substituted juglones with either electron-withdrawing or -donating substituents are regioselectively oxidized to o- or p-naphthoquinones using salcomine/air or [bis(trifluoroacetoxy)iodo]benzene, respectively. The structure of the oxidation products was confirmed by chemical transformations. A correlation between chemical shift of the single quinoid proton and the quinone structure was established. (C) 2000 Elsevier Science Ltd. All rights reserved. |
en |
heal.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
en |
heal.journalName |
TETRAHEDRON LETTERS |
en |
dc.identifier.issue |
4 |
en |
dc.identifier.volume |
41 |
en |
dc.identifier.isi |
ISI:000084947700023 |
en |
dc.identifier.spage |
535 |
en |
dc.identifier.epage |
538 |
en |