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dc.contributor.authorPatre, R.E.
dc.contributor.authorShet, J.B.
dc.contributor.authorParameswaran, P.S.
dc.contributor.authorTilve, S.G.
dc.date.accessioned2009-10-09T10:46:45Z
dc.date.available2009-10-09T10:46:45Z
dc.date.issued2009
dc.identifier.citationTetrahedron Letters, vol.50(47); 6488–6490
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/3414
dc.description.abstractA cascade Wittig reaction-double Claisen and Cope rearrangements has been employed for a one-pot synthesis of diprenylated coumarins gravelliferone, balsamiferone, and 6,8-diprenylumbelliferone from a common precursor 2,4-diprenyloxybenzaldehyde
dc.language.isoen
dc.publisherElsevier
dc.rightsAn edited version of this paper was published by Elsevier. Copyright [2009] Elsevier
dc.subjectmolecular structure
dc.subjectchemical reaction
dc.subjectbioactive compounds
dc.subjectdrugs
dc.titleCascade Wittig reaction-double Claisen and Cope rearrangements: one-pot synthesis of diprenylated coumarins gravelliferone, balsamiferone, and 6,8-diprenylumbelliferone
dc.typeJournal Article


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