Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60509
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dc.contributor.authorMamedov, I G-
dc.contributor.authorMamedov, E I-
dc.date.accessioned2022-09-19T10:17:23Z-
dc.date.available2022-09-19T10:17:23Z-
dc.date.issued2022-09-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60509-
dc.description961-964en_US
dc.description.abstractA two-component Claisen-Schmidt condensation between the 2-hydoxy-5-methylacetophenone and some aromatic aldehydes has been carried out for the synthesis of chalcone derivatives at ambient temperature. The products have been obtained with good yields and as a mixture of two compounds or a single product. Piperidine has been used as a catalyst for the in situ generation of carbanion from ketone. The possibility of the formation of different products has been investigated on the based PM7 optimization, HMO theory and NMR methods.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(09) [Sep 2022]en_US
dc.subjectKetoneen_US
dc.subjectaldehydeen_US
dc.subjectchalconeen_US
dc.subjectchromenoneen_US
dc.subjectNMRen_US
dc.subjectmolecular modelingen_US
dc.titleCharacterization of the 2-hydroxy-5-methylacetophenone and some aromatıc aldehydes condensation products by NMR and computational methodsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i9.66347en_US
Appears in Collections:IJC Vol.61(09) [Sep 2022]

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