Exhaustive Suzuki-Miyaura Reactions of Polyhalogenated Heteroarenes with Alkyl Boronic Pinacol Esters
| dc.contributor.author | Laulhé, Sébastien | |
| dc.contributor.author | Blackburn, J. Miles | |
| dc.contributor.author | Roizen, Jennifer L. | |
| dc.contributor.department | Chemistry and Chemical Biology, School of Science | en_US |
| dc.date.accessioned | 2019-01-18T14:12:49Z | |
| dc.date.available | 2019-01-18T14:12:49Z | |
| dc.date.issued | 2017-06-29 | |
| dc.description.abstract | A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. | en_US |
| dc.eprint.version | Author's manuscript | en_US |
| dc.identifier.citation | Laulhé, S., Blackburn, J. M., & Roizen, J. L. (2017). Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol esters. Chemical communications (Cambridge, England), 53(53), 7270-7273. | en_US |
| dc.identifier.uri | https://hdl.handle.net/1805/18194 | |
| dc.language.iso | en_US | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.relation.isversionof | 10.1039/c7cc00997f | en_US |
| dc.relation.journal | Chemical communications (Cambridge, England) | en_US |
| dc.rights | Publisher Policy | en_US |
| dc.source | PMC | en_US |
| dc.subject | Suzuki-Miyaura Reactions | en_US |
| dc.subject | Polyhalogenated heteroarenes | en_US |
| dc.subject | Alkyl boronic pinacol esters | en_US |
| dc.subject | Stable heteroaryl chlorides | en_US |
| dc.subject | Cross-coupling reaction | en_US |
| dc.subject | Commercially available reagents | en_US |
| dc.subject | Reduced toxicity | en_US |
| dc.subject | Formal synthesis of normuscopyridine | en_US |
| dc.title | Exhaustive Suzuki-Miyaura Reactions of Polyhalogenated Heteroarenes with Alkyl Boronic Pinacol Esters | en_US |
| dc.type | Article | en_US |