| dc.contributor.author | SENGE, MATHIAS | en |
| dc.date.accessioned | 2009-07-06T16:46:23Z | |
| dc.date.available | 2009-07-06T16:46:23Z | |
| dc.date.issued | 2009 | en |
| dc.date.submitted | 2009 | en |
| dc.identifier.citation | Oliver B. Locos, Katja Dahms and Mathias O. Senge, Allenylporphyrins: a new motif on the porphyrin periphery, Tetrahedron Letters, 50, 21, 2009, 2566 - 2569 | en |
| dc.identifier.other | Y | en |
| dc.identifier.uri | http://hdl.handle.net/2262/31346 | |
| dc.description | PUBLISHED | en |
| dc.description.abstract | Palladium-catalysed Suzuki?Miyaura cross-coupling proved to be the simplest and most efficient method for attaching an unsubstituted allene, a novel substituent and potential functional group, to the porphyrin periphery. Comparative studies on various allenyl synthetic pathways show that this method, which makes use of a bromoporphyrin and allenylboronate, affords the corresponding allenylporphyrin in the presence of an appropriate base and THF. | en |
| dc.format.extent | 2566 | en |
| dc.format.extent | 2569 | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | Tetrahedron Letters | en |
| dc.relation.ispartofseries | 50 | en |
| dc.relation.ispartofseries | 21 | en |
| dc.rights | Y | en |
| dc.subject | Chemistry | en |
| dc.title | Allenylporphyrins: a new motif on the porphyrin periphery | en |
| dc.type | Journal Article | en |
| dc.contributor.sponsor | Science Foundation Ireland (SFI) | en |
| dc.type.supercollection | scholarly_publications | en |
| dc.type.supercollection | refereed_publications | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/sengem | en |
| dc.identifier.rssinternalid | 59670 | en |
| dc.identifier.doi | http://dx.doi.org/10.1016/j.tetlet.2009.03.097 | en |
