Decarboxylative Arylation of Substituted Pyrroles N-protected with 2-(Trimethylsilyl) ethoxymethyl (SEM)
| dc.contributor.author | Figliola, Carlotta | |
| dc.contributor.author | Greening, Sarah | |
| dc.contributor.author | Lamont, Connor | |
| dc.contributor.author | Groves, Brandon R. | |
| dc.contributor.author | Thompson, Alison | |
| dc.date.accessioned | 2018-10-29T17:14:24Z | |
| dc.date.available | 2018-10-29T17:14:24Z | |
| dc.date.issued | 2018 | |
| dc.identifier.citation | Figliola, C., Greening, S. M., Lamont, C., Groves, B. R., & Thompson, A. (2018). Decarboxylative arylation of substituted pyrroles N-protected with 2-(trimethylsilyl) ethoxymethyl (SEM). Canadian Journal of Chemistry, 96(6), 534-542. doi: https://doi.org/10.1139/cjc-2017-0402 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10222/74917 | |
| dc.description | Post-print | en_US |
| dc.description.abstract | Palladium-catalyzed decarboxylative arylation is reported using pyrroles N-protected with the 2-(trimethylsilyl) ethoxymethyl (SEM) group and featuring 2-, 3- and 4-substituents about the pyrrolic framework. In contrast to N-protected pyrroles previously used in decarboxylative arylation, the use of SEM allows deprotection under mild conditions. | en_US |
| dc.publisher | Canadian Journal of Chemistry | en_US |
| dc.title | Decarboxylative Arylation of Substituted Pyrroles N-protected with 2-(Trimethylsilyl) ethoxymethyl (SEM) | en_US |
| dc.type | Article | en_US |
