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/2440/105989
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDay, A.-
dc.contributor.authorLamr, H.-
dc.contributor.authorSumby, C.-
dc.contributor.authorGeorge, J.-
dc.date.issued2017-
dc.identifier.citationOrganic Letters, 2017; 19(10):2463-2465-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/105989-
dc.description.abstractA divergent, three-step total synthesis of rhodonoids C and D has been achieved using a biosynthetically inspired, acid-catalyzed cascade cyclization of an epoxy-chromene that involves the presumed intermediacy of o-quinone methides. Application of a similar strategy also allowed synthesis of the alkaloid murrayakonine D.-
dc.description.statementofresponsibilityAaron J. Day, Hiu C. Lam, Christopher J. Sumby and Jonathan H. George-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.rights© 2017 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/acs.orglett.7b00779-
dc.subjectTerpenes-
dc.subjectBenzopyrans-
dc.subjectBiomimetics-
dc.subjectMolecular Structure-
dc.subjectCyclization-
dc.subjectStereoisomerism-
dc.titleBiomimetic total synthesis of rhodonoids C and D, and murrayakonine D-
dc.typeJournal article-
dc.identifier.doi10.1021/acs.orglett.7b00779-
dc.relation.granthttp://purl.org/au-research/grants/arc/DP160103393-
pubs.publication-statusPublished-
dc.identifier.orcidSumby, C. [0000-0002-9713-9599]-
dc.identifier.orcidGeorge, J. [0000-0002-7330-2160]-
Appears in Collections:Aurora harvest 3
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.