| dc.contributor.author | Timothy J Donohoe | |
| dc.contributor.author | Paul M Guyo | |
| dc.contributor.author | Rakesh R Harji | |
| dc.contributor.author | Madeleine Helliwell | |
| dc.date.accessioned | 2012-10-23T11:14:42Z | |
| dc.date.available | 2012-10-23T11:14:42Z | |
| dc.date.issued | 1998-05-07 | |
| dc.identifier.citation | . Volume 39, Issue 19, 7 May 1998, Pages 3075–3078 | en_US |
| dc.identifier.uri | http://hdl.handle.net/123456789/332 | |
| dc.description | The original publication is available at http://www.sciencedirect.com/science/article/pii/S0040403998003621 | en_US |
| dc.description.abstract | The Birchreduction of electron-deficient 3-substituted pyrroles is described. Use of a reductive alkylation procedure involving sodium metal in liquid ammonia gave good yields of 4-alkyl-2-pyrrolines. The identity of these products was proven by an X-ray structure of a crystalline derivative. Moreover, the pyrroles used in this study could be readily prepared by reaction of TOSMIC with acrylic amides and esters and, once the reduction was complete, the ester activating group could be easily removed to yield the corresponding N-protected β-proline derivatives. | en_US |
| dc.description.sponsorship | Pwani University | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | ELSELVIER | en_US |
| dc.subject | Birch | en_US |
| dc.subject | pyrroles | en_US |
| dc.subject | reduction | en_US |
| dc.title | The Birchreduction of 3-substituted pyrroles | en_US |
| dc.type | Article | en_US |
