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Ruthenium-catalyzed selective hydrogenation of bis-arylidene tetramic acids. Application to the synthesis of novel structurally diverse pyrrolidine-2,4-diones

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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


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