Publication: Selenium-Catalyzed C(sp(3))-H Acyloxylation: Application in the Expedient Synthesis of Isobenzofuranones
| dc.bibliographiccitation.firstpage | 7030 | |
| dc.bibliographiccitation.issue | 19 | |
| dc.bibliographiccitation.journal | Chemistry - A European Journal | |
| dc.bibliographiccitation.lastpage | 7034 | |
| dc.bibliographiccitation.volume | 21 | |
| dc.contributor.author | Kraetzschmar, Felix | |
| dc.contributor.author | Kassel, Martin | |
| dc.contributor.author | Delony, Daniel | |
| dc.contributor.author | Breder, Alexander | |
| dc.date.accessioned | 2018-11-07T09:57:22Z | |
| dc.date.available | 2018-11-07T09:57:22Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | Oxidative 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.doi | 10.1002/chem.201406290 | |
| dc.identifier.isi | 000353348100008 | |
| dc.identifier.pmid | 25808950 | |
| dc.identifier.uri | https://resolver.sub.uni-goettingen.de/purl?gro-2/37143 | |
| dc.notes.status | zu prüfen | |
| dc.notes.submitter | Najko | |
| dc.publisher | Wiley-v C H Verlag Gmbh | |
| dc.relation.issn | 1521-3765 | |
| dc.relation.issn | 0947-6539 | |
| dc.title | Selenium-Catalyzed C(sp(3))-H Acyloxylation: Application in the Expedient Synthesis of Isobenzofuranones | |
| dc.type | journal_article | |
| dc.type.internalPublication | yes | |
| dc.type.peerReviewed | yes | |
| dc.type.status | published | |
| dspace.entity.type | Publication |