Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/36525
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Taylor, D. | - |
dc.date.issued | 2002 | - |
dc.identifier.uri | http://hdl.handle.net/2440/36525 | - |
dc.description | Publication Number: WO/2002/079136 International Application No.: PCT/AU2002/000417 Publication Date: 10.10.2002 International Filing Date: 02.04.2002 | - |
dc.description.abstract | A 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.iso | en | - |
dc.source.uri | http://www.freepatentsonline.com/WO2002079136.html | - |
dc.title | Enantiomerically selective cyclopropanation | - |
dc.type | Patent | - |
dc.contributor.assignee | The University of Adelaide | - |
dc.identifier.patent | WO/2002/079136 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Taylor, D. [0000-0002-3302-4610] [0000-0002-4274-3983] [0000-0003-0633-7424] | - |
Appears in Collections: | Aurora harvest 6 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.