Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1844
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dc.contributor.authorJadhav, A.S.-
dc.contributor.authorPankhade, Y.A.-
dc.contributor.authorHazra, R.-
dc.contributor.authorAnand, R.V.-
dc.date.accessioned2020-11-19T05:49:19Z-
dc.date.available2020-11-19T05:49:19Z-
dc.date.issued2018-
dc.identifier.citationJournal of Organic Chemistry, 83(17), pp. 10107–10119en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.joc.8b01401-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.8b01401-
dc.identifier.urihttp://hdl.handle.net/123456789/1844-
dc.description.abstractA Lewis acid-catalyzed intermolecular 1,6-hydroolefination of p-quinone methides with styrenes leading to vinyl diarylmethanes and indenes has been developed. This protocol was also elaborated to the total synthesis of (±)-isopaucifloral F. Besides, interestingly, the reaction between 2-alkynylated p-quinone methides and styrenes provided a straightforward access to dihydrobenzo[a]fluorene derivatives in one pot with 100% atom-economyen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCyclizationen_US
dc.subjectCascade cyclizationen_US
dc.subjectDiarylmethanesen_US
dc.subjectp-Quinone methidesen_US
dc.title1,6-Hydroolefination and Cascade Cyclization of p-Quinone Methides with Styrenes: Total Synthesis of (±)-Isopaucifloral Fen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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