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https://hdl.handle.net/2440/86624
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DC Field | Value | Language |
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dc.contributor.author | Abell, A.D. | - |
dc.contributor.author | Horn, E. | - |
dc.contributor.author | Jones, G.P. | - |
dc.contributor.author | Snow, M.R. | - |
dc.contributor.author | Massywestropp, R.A. | - |
dc.contributor.author | Riccio, R. | - |
dc.date.issued | 1985 | - |
dc.identifier.citation | Australian Journal of Chemistry: an international journal for chemical science, 1985; 38(12):1837-1845 | - |
dc.identifier.issn | 0004-9425 | - |
dc.identifier.issn | 1445-0038 | - |
dc.identifier.uri | http://hdl.handle.net/2440/86624 | - |
dc.description.abstract | The 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.statementofresponsibility | AD Abell, E Horn, GP Jones, MR Snow, RA Massywestropp and R Riccio | - |
dc.language.iso | en | - |
dc.publisher | CSIRO Publishing | - |
dc.rights | © CSIRO 1985 | - |
dc.source.uri | http://dx.doi.org/10.1071/ch9851837 | - |
dc.title | The structure of a stable serrulatane diterpenoid acetal from eremophila rotundifolia | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1071/CH9851837 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Abell, A.D. [0000-0002-0604-2629] | - |
Appears in Collections: | Aurora harvest 7 Chemistry publications |
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