Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/36525
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dc.contributor.authorTaylor, D.-
dc.date.issued2002-
dc.identifier.urihttp://hdl.handle.net/2440/36525-
dc.descriptionPublication Number: WO/2002/079136 International Application No.: PCT/AU2002/000417 Publication Date: 10.10.2002 International Filing Date: 02.04.2002-
dc.description.abstractA method of forming a cyclopropane having enhanced chirality said method comprising reacting together (1), a symmetrical 1,2-dioxine of the formula (1), wherein X and Y are the same and are groups in which a carbon atom is bonded to the dioxine backbone; and a phosphorus ylide or a phosphorus ylide precursor; in the presence of a cobalt catalyst containing a chiral ligand.-
dc.language.isoen-
dc.source.urihttp://www.freepatentsonline.com/WO2002079136.html-
dc.titleEnantiomerically selective cyclopropanation-
dc.typePatent-
dc.contributor.assigneeThe University of Adelaide-
dc.identifier.patentWO/2002/079136-
pubs.publication-statusPublished-
dc.identifier.orcidTaylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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