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dc.contributor.authorV. Sapegin, Alexander
dc.contributor.authorA. Kalinin, Stanislav
dc.contributor.authorV. Smirnov, Alexey
dc.contributor.authorV. Dorogov, Mikhail
dc.contributor.authorKrasavin, Mikhail
dc.date.accessioned2019-02-22T01:53:39Z
dc.date.available2019-02-22T01:53:39Z
dc.date.issued2014
dc.identifier.issn14645416
dc.identifier.doi10.1016/j.tet.2013.12.026
dc.identifier.urihttp://hdl.handle.net/10072/112815
dc.description.abstractA streamlined synthetic methodology towards novel tetracyclic 1,4-oxazepines from readily available precursors is described. The compounds, designed as more soluble version of the earlier described, poorly soluble dibenzo[b,f][1,4]oxazepines, were obtained in high yields and as a single regioisomer as a result of three tandem chemical events-nucleophilic aromatic substitution, Smiles rearrangement and denitrocyclization.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherElsevier
dc.publisher.placeUnited Kingdom
dc.relation.ispartofpagefrom1077
dc.relation.ispartofpageto1083
dc.relation.ispartofissue5
dc.relation.ispartofjournalTetrahedron
dc.relation.ispartofvolume70
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry not elsewhere classified
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode030499
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleNew tetracyclic 1,4-oxazepines constructed via practically simple tandem condensation strategy from readily available synthons
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.hasfulltextNo Full Text
gro.griffith.authorKrasavin, Mikhail


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