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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/115784
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dc.contributor.authorFerrer, C.-
dc.contributor.authorFodran, P.-
dc.contributor.authorBarroso, S.-
dc.contributor.authorGibson, R.-
dc.contributor.authorHopmans, E.-
dc.contributor.authorDamsté, J.-
dc.contributor.authorSchouten, S.-
dc.contributor.authorMinnaard, A.-
dc.date.issued2013-
dc.identifier.citationOrganic and Biomolecular Chemistry, 2013; 11(15):2482-2492-
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttp://hdl.handle.net/2440/115784-
dc.description.abstractAn efficient asymmetric synthesis of cyclo-archaeol and β-glucosyl cyclo-archaeol is presented employing catalytic asymmetric conjugate addition and catalytic epoxide ring opening as the key steps. Their occurrence in deep sea hydrothermal vents has been confirmed by chromatographic comparison with natural samples.-
dc.description.statementofresponsibilityCatalina Ferrer, Peter Fodran, Santiago Barroso, Robert Gibson, Ellen C. Hopmans, Jaap Sinninghe Damsté, Stefan Schouten and Adriaan J. Minnaard-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsThis journal is © The Royal Society of Chemistry 2013-
dc.source.urihttp://dx.doi.org/10.1039/c3ob27277j-
dc.subjectGlycerophospholipids-
dc.titleAsymmetric synthesis of cyclo-archaeol and β-glucosyl cyclo-archaeol-
dc.title.alternativeAsymmetric synthesis of cyclo-archaeol and beta-glucosyl cyclo-archaeol-
dc.typeJournal article-
dc.identifier.doi10.1039/c3ob27277j-
pubs.publication-statusPublished-
dc.identifier.orcidGibson, R. [0000-0002-8750-525X]-
Appears in Collections:Agriculture, Food and Wine publications
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