| dc.contributor.author | SCANLAN, EOIN | en |
| dc.date.accessioned | 2014-11-24T16:34:15Z | |
| dc.date.available | 2014-11-24T16:34:15Z | |
| dc.date.issued | 2008 | en |
| dc.date.submitted | 2008 | en |
| dc.identifier.citation | Portela-Cubillo, F, Scanlan, EM, Scott, JS, Walton, JC, From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals., Chemical communications (Cambridge, England), 35, 2008, 4189-4191 | en |
| dc.identifier.other | Y | en |
| dc.description | PUBLISHED | en |
| dc.description.abstract | Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines. | en |
| dc.format.extent | 4189-4191 | en |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | Chemical communications (Cambridge, England) | en |
| dc.relation.ispartofseries | 35 | en |
| dc.rights | Y | en |
| dc.subject | Chemistry | en |
| dc.title | From dioxime oxalates to dihydropyrroles and phenanthridines via iminyl radicals. | en |
| dc.type | Journal Article | en |
| dc.type.supercollection | scholarly_publications | en |
| dc.type.supercollection | refereed_publications | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/scanlae | en |
| dc.identifier.rssinternalid | 55669 | en |
| dc.identifier.doi | http://dx.doi.org/10.1039/B808625G | en |
| dc.rights.ecaccessrights | openAccess | |
| dc.identifier.uri | http://hdl.handle.net/2262/72174 | |
