dc.contributor.author |
Karaiskos, CS |
en |
dc.contributor.author |
Matiadis, D |
en |
dc.contributor.author |
Markopoulos, J |
en |
dc.contributor.author |
Igglessi-Markopoulou, O |
en |
dc.date.accessioned |
2014-03-01T01:36:43Z |
|
dc.date.available |
2014-03-01T01:36:43Z |
|
dc.date.issued |
2011 |
en |
dc.identifier.issn |
1420-3049 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/21413 |
|
dc.subject |
Arylidenetetramic acid |
en |
dc.subject |
BINAP |
en |
dc.subject |
Homogeneous catalysis |
en |
dc.subject |
Hydrogenation |
en |
dc.subject |
Ruthenium catalysts |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
2 pyrrolidone derivative |
en |
dc.subject.other |
pyrrolidine |
en |
dc.subject.other |
pyrrolidine derivative |
en |
dc.subject.other |
ruthenium |
en |
dc.subject.other |
tetramic acid |
en |
dc.subject.other |
article |
en |
dc.subject.other |
catalysis |
en |
dc.subject.other |
chemistry |
en |
dc.subject.other |
hydrogenation |
en |
dc.subject.other |
stereoisomerism |
en |
dc.subject.other |
Catalysis |
en |
dc.subject.other |
Hydrogenation |
en |
dc.subject.other |
Pyrrolidines |
en |
dc.subject.other |
Pyrrolidinones |
en |
dc.subject.other |
Ruthenium |
en |
dc.subject.other |
Stereoisomerism |
en |
dc.title |
Ruthenium-catalyzed selective hydrogenation of bis-arylidene tetramic acids. Application to the synthesis of novel structurally diverse pyrrolidine-2,4-diones |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.3390/molecules16076116 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.3390/molecules16076116 |
en |
heal.language |
English |
en |
heal.publicationDate |
2011 |
en |
heal.abstract |
Catalytic hydrogenation of 3,5-bis-arylidenetetramic acids, known for their biological activity, has been developed. The chemoselective ruthenium-catalyzed reduction of the exocyclic carbon-carbon double bonds on pyrrolidine-2,4-dione ring system, containing other reducible functions, has been investigated. Depending on the substrate the yield of the hydrogenation process can reach up to 95%. The structural elucidation has been established using NMR and HRMS spectral data. © 2011 by the authors; licensee MDPI, Basel, Switzerland. |
en |
heal.publisher |
MDPI AG |
en |
heal.journalName |
Molecules |
en |
dc.identifier.doi |
10.3390/molecules16076116 |
en |
dc.identifier.isi |
ISI:000293073900060 |
en |
dc.identifier.volume |
16 |
en |
dc.identifier.issue |
7 |
en |
dc.identifier.spage |
6116 |
en |
dc.identifier.epage |
6128 |
en |