Publication:
Selenium-Catalyzed C(sp(3))-H Acyloxylation: Application in the Expedient Synthesis of Isobenzofuranones

dc.bibliographiccitation.firstpage7030
dc.bibliographiccitation.issue19
dc.bibliographiccitation.journalChemistry - A European Journal
dc.bibliographiccitation.lastpage7034
dc.bibliographiccitation.volume21
dc.contributor.authorKraetzschmar, Felix
dc.contributor.authorKassel, Martin
dc.contributor.authorDelony, Daniel
dc.contributor.authorBreder, Alexander
dc.date.accessioned2018-11-07T09:57:22Z
dc.date.available2018-11-07T09:57:22Z
dc.date.issued2015
dc.description.abstractOxidative Se-catalyzed C(sp(3))H bond acyloxylation has been used to construct a diverse array of isobenzofuranones from simple ortho-allyl benzoic acid derivatives. The synthetic procedure employs mild reaction conditions and gives high chemoselectivity enabled by an inexpensive organodiselane catalyst. The presented approach offers a new synthetic pathway toward the core structures of phthalide natural products.
dc.identifier.doi10.1002/chem.201406290
dc.identifier.isi000353348100008
dc.identifier.pmid25808950
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/37143
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherWiley-v C H Verlag Gmbh
dc.relation.issn1521-3765
dc.relation.issn0947-6539
dc.titleSelenium-Catalyzed C(sp(3))-H Acyloxylation: Application in the Expedient Synthesis of Isobenzofuranones
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dspace.entity.typePublication

Files

Collections