Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5321
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dc.contributor.authorKakde, Badrinath N.en_US
dc.contributor.authorParida, Amarchanden_US
dc.contributor.authorKUMARI, POOJAen_US
dc.contributor.authorBisai, Alakeshen_US
dc.date.accessioned2020-10-26T10:55:29Z-
dc.date.available2020-10-26T10:55:29Z-
dc.date.issued2016-07en_US
dc.identifier.citationTetrahedron Letters, 57(29), 3179-3184.en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5321-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2016.06.030en_US
dc.description.abstractTotal syntheses of structurally intriguing taiwaniaquinoids viz (±)-taiwaniaquinol D (1e) and (±)-taiwaniaquinone D (1h) have been disclosed via a key Lewis acid catalyzed Nazarov type cyclization of arylvinylcarbinols.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectabeo-Abietaneen_US
dc.subjectTotal synthesisen_US
dc.subjectNazarov cyclizationen_US
dc.subjectQuaternary stereocenteren_US
dc.subjectTaiwaniaquinoidsen_US
dc.subject2016en_US
dc.titleTotal syntheses of (+/-)-taiwaniaquinol D and (+/-)-taiwaniaquinone D via a key Lewis acid-catalyzed Nazarov type cyclizationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleTetrahedron Lettersen_US
dc.publication.originofpublisherForeignen_US
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