Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9421
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:57Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:57Z-
dc.date.issued2013-
dc.identifier.citationAyyagari, N., Mehta, A., Gopi, E., Deb, I., Mobin, S. M., & Namboothiri, I. N. N. (2013). Conjugate addition of curcumins to chalcones and azodicarboxylates. Tetrahedron, 69(29), 5973-5980. doi:10.1016/j.tet.2013.04.083en_US
dc.identifier.issn0040-4020-
dc.identifier.otherEID(2-s2.0-84878888069)-
dc.identifier.urihttps://doi.org/10.1016/j.tet.2013.04.083-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9421-
dc.description.abstractCascade double Michael reaction of curcumins with chalcones in the presence of Cs2CO3 in CH3CN provided highly functionalized cyclohexanones in moderate to good yields (35-77%) and good to excellent diastereoselectivities (81:19 to 95:05). Similar reaction of curcumins with azodicarboxylates in the presence of DMAP in CH3CN stopped at the single Michael addition stage affording novel hydrazinodicarboxylates of curcumins in good to excellent yields (65-85%). © 2013 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.sourceTetrahedronen_US
dc.subjectazodicarboxylic acid derivativeen_US
dc.subjectcarboxylic acid derivativeen_US
dc.subjectchalconeen_US
dc.subjectcurcuminen_US
dc.subjecthydrazine derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectarticleen_US
dc.subjectconjugateen_US
dc.subjectdiastereoisomeren_US
dc.subjectdrug structureen_US
dc.subjectdrug synthesisen_US
dc.subjectMichael additionen_US
dc.subjectpriority journalen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectreaction optimizationen_US
dc.subjectstereochemistryen_US
dc.titleConjugate addition of curcumins to chalcones and azodicarboxylatesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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