Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2587
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dc.contributor.authorMahesh, S.-
dc.contributor.authorKant, Guddi-
dc.contributor.authorAnand, R.V.-
dc.date.accessioned2020-12-03T09:33:59Z-
dc.date.available2020-12-03T09:33:59Z-
dc.date.issued2016-
dc.identifier.citationRSC Advances, 6(81), pp. 80718-80722en_US
dc.identifier.otherDOI: 10.1039/C6RA19069C-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlehtml/2016/ra/c6ra19069c-
dc.identifier.urihttp://hdl.handle.net/123456789/2587-
dc.description.abstractAn effective method for the synthesis of unsymmetrical allyldiaryl methanes is portrayed. This protocol involves a Lewis acid catalysed 1,6-conjugate addition of allyltrimethyl silanes to para-quinone methides, which enabled us to synthesize a variety of unsymmetrical allyl diarylmethanes in good to excellent yields in a very short reaction period.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subject1 ,6-conjugate additionsen_US
dc.subjectDiarylmethanesen_US
dc.subjectAllyldiaryl methanesen_US
dc.subjectPara-quinone methidesen_US
dc.titleB(C6F5)3 catalysed 1,6-conjugate allylation of para-quinone methides: expedient access to allyl diarylmethanesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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