Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/86624
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAbell, A.D.-
dc.contributor.authorHorn, E.-
dc.contributor.authorJones, G.P.-
dc.contributor.authorSnow, M.R.-
dc.contributor.authorMassywestropp, R.A.-
dc.contributor.authorRiccio, R.-
dc.date.issued1985-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 1985; 38(12):1837-1845-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/86624-
dc.description.abstractThe serrulatenol (1a), a stable diterpenoid acetal from remophilia rotundifolia, has been shown to be (13S,18R)-5,18:13,18- diepoxyserrulat-14-en-8-ol by chemical and spectroscopic characterization and by single-crystal X-ray analysis of the p- bromobenzoate . This compound crystallizes as clear prisms in the monoclinic space group P21 with a 9.112(1), b 9.743(2), c 13.423(3) Ǻ, β 102.27(5)° and Z 2. The structural final refinement of a blocked-matrix least-squares calculation converged with R 0.038 and Rw 0.041.-
dc.description.statementofresponsibilityAD Abell, E Horn, GP Jones, MR Snow, RA Massywestropp and R Riccio-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.rights© CSIRO 1985-
dc.source.urihttp://dx.doi.org/10.1071/ch9851837-
dc.titleThe structure of a stable serrulatane diterpenoid acetal from eremophila rotundifolia-
dc.typeJournal article-
dc.identifier.doi10.1071/CH9851837-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A.D. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 7
Chemistry publications

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


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