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dc.contributor.authorParvatkar, P.T.
dc.contributor.authorKadam, H.K.
dc.contributor.authorTilve, S.G.
dc.date.accessioned2014-09-04T07:08:47Z
dc.date.available2014-09-04T07:08:47Z
dc.date.issued2014
dc.identifier.citationTetrahedron, vol.70(18); 2014; 2857-2888.
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/4593
dc.description.abstractThis review summarizes the recent examples of tandem or sequential reactions used for the last 10 years for the synthesis of fused and bridged bicyclic or polycyclic compounds with IMDA cycloaddition as the key means to access these compounds. Tandem or sequential processes are economically highly efficient and if properly planned and executed can provide facile route for the synthesis of complex natural product skeletons.
dc.language.isoen
dc.publisherElsevier
dc.rightsAn edited version of this paper was published by Elsevier. Copyright [2014] Elsevier
dc.subjectNatural product
dc.subjectSequential
dc.titleIntramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds.
dc.typeJournal Article


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