Synthesis of symmetric meso-H dipyrrin hydrobromides from 2-formyl pyrroles
| dc.contributor.author | Lund, Kate-lyn A.R. | |
| dc.contributor.author | Thompson, Alison | |
| dc.date.accessioned | 2018-11-14T18:30:36Z | |
| dc.date.available | 2018-11-14T18:30:36Z | |
| dc.date.issued | 2014 | |
| dc.description | - Post-print - Publisher copyright and source must be acknowledged - Link to Publisher version (www.thieme-connect.com) must be included if article has been published online | en_US |
| dc.description.abstract | The reaction of 2-formyl pyrroles in acidic methanol gives the corresponding symmetric, meso-H 4,6-dipyrrin hydrobromides. This convenient strategy involves initial deformylation under the acidic conditions, followed by immediate in situ reaction of the resulting α-free pyrrole with the remaining 2-formyl pyrrole in solution to give the dipyrrin hydrobromide salt in good yield. | en_US |
| dc.identifier.citation | Lund, K. L. A., & Thompson, A. (2014). Synthesis of Symmetric meso-H-Dipyrrin Hydrobromides from 2-Formylpyrroles. Synlett, 25(08), 1142-1144. DOI: 10.1055/s-0033-1341066 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10222/74956 | |
| dc.publisher | Synlett | en_US |
| dc.title | Synthesis of symmetric meso-H dipyrrin hydrobromides from 2-formyl pyrroles | en_US |
| dc.type | Article | en_US |