Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9427
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:59Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:59Z-
dc.date.issued2013-
dc.identifier.citationKumar, T., Mobin, S. M., & Namboothiri, I. N. N. (2013). Regiospecific synthesis of arenofurans via cascade reactions of arenols with morita-baylis-hillman acetates of nitroalkenes and total synthesis of isoparvifuran. Tetrahedron, 69(24), 4964-4972. doi:10.1016/j.tet.2013.04.023en_US
dc.identifier.issn0040-4020-
dc.identifier.otherEID(2-s2.0-84877584892)-
dc.identifier.urihttps://doi.org/10.1016/j.tet.2013.04.023-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9427-
dc.description.abstractA cascade process involving an SN2′ reaction and an intramolecular oxa-Michael addition has been developed by treating Morita-Baylis-Hillman acetates of nitroalkenes with arenols, such as β-naphthols, α-naphthols, and substituted phenols under basic conditions. The products, arenofurans, are formed as single regioisomers in good to excellent yield in most cases. The methodology has been successfully employed for the total synthesis of an anti fungal agent isoparvifuran. © 2013 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.sourceTetrahedronen_US
dc.subject1 naphtholen_US
dc.subject2 naphtholen_US
dc.subjectacetic acid derivativeen_US
dc.subjectalkene derivativeen_US
dc.subjectantifungal agenten_US
dc.subjectarenofuran derivativeen_US
dc.subjectfuran derivativeen_US
dc.subjectisoparvifuranen_US
dc.subjectMorita Baylis Hillman acetateen_US
dc.subjectnitroalkene derivativeen_US
dc.subjectphenol derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectarticleen_US
dc.subjectmethodologyen_US
dc.subjectMichael additionen_US
dc.subjectpriority journalen_US
dc.subjectsynthesisen_US
dc.titleRegiospecific synthesis of arenofurans via cascade reactions of arenols with Morita-Baylis-Hillman acetates of nitroalkenes and total synthesis of isoparvifuranen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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