1. Adelaide Research & Scholarship
  2. Schools and Disciplines
  3. School of Chemistry and Physics
  4. Chemistry
  5. Chemistry publications
Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/106799
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPepper, H.-
dc.contributor.authorLam, H.-
dc.contributor.authorGeorge, J.-
dc.date.issued2017-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2017; 15(22):4811-4815-
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttp://hdl.handle.net/2440/106799-
dc.description.abstractThe synthesis of verrubenzospirolactone from its proposed biosynthetic precursor, capillobenzopyranol, has been shown to be chemically feasible via a simple reaction sequence. The key steps are a chemoselective furan oxidation mediated by NaClO₂, a stereoselective dehydration of a γ-methoxybutenolide, and an intramolecular Diels-Alder reaction.-
dc.description.statementofresponsibilityHenry P. Pepper, Hiu C. Lam and Jonathan H. George-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2017-
dc.source.urihttp://dx.doi.org/10.1039/c7ob00868f-
dc.titleBiosynthetically-inspired oxidations of capillobenzopyranol-
dc.typeJournal article-
dc.identifier.doi10.1039/c7ob00868f-
dc.relation.granthttp://purl.org/au-research/grants/arc/DP160103393-
pubs.publication-statusPublished-
dc.identifier.orcidGeorge, J. [0000-0002-7330-2160]-
Appears in Collections:Aurora harvest 8
Chemistry publications

Files in This Item:
There are no files associated with this item.
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.