Synthesis of a benzene-annulated analogue of resolving E1 and other lipid mediators
dc.contributor.author | Lombardo, Daniel Mario | |
dc.contributor.supervisor | Dr Alan Payne | |
dc.date.accessioned | 2017-01-30T09:48:55Z | |
dc.date.available | 2017-01-30T09:48:55Z | |
dc.date.created | 2015-06-10T03:08:40Z | |
dc.date.issued | 2015 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/337 | |
dc.description.abstract |
The resolvins are a class of short-lived, naturally occurring compounds with potent anti-inflammatory effects. Using a sequential Sonogashira-Stille reaction, the formal total synthesis of resolvin E1 and the synthesis of a benzene annulated analogue of this compound were completed. The fusion of the benzene ring improves the stability and retains the molecules activity towards the BLT-1 receptor. | |
dc.language | en | |
dc.publisher | Curtin University | |
dc.title | Synthesis of a benzene-annulated analogue of resolving E1 and other lipid mediators | |
dc.type | Thesis | |
dcterms.educationLevel | PhD | |
curtin.department | Department of Chemistry | |
curtin.accessStatus | Open access |