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Decarboxylative Arylation of Substituted Pyrroles N-protected with 2-(Trimethylsilyl) ethoxymethyl (SEM)

dc.contributor.authorFigliola, Carlotta
dc.contributor.authorGreening, Sarah
dc.contributor.authorLamont, Connor
dc.contributor.authorGroves, Brandon R.
dc.contributor.authorThompson, Alison
dc.date.accessioned2018-10-29T17:14:24Z
dc.date.available2018-10-29T17:14:24Z
dc.date.issued2018
dc.descriptionPost-printen_US
dc.description.abstractPalladium-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.identifier.citationFigliola, 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-2017-0402en_US
dc.identifier.urihttp://hdl.handle.net/10222/74917
dc.publisherCanadian Journal of Chemistryen_US
dc.titleDecarboxylative Arylation of Substituted Pyrroles N-protected with 2-(Trimethylsilyl) ethoxymethyl (SEM)en_US
dc.typeArticleen_US

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