| dc.contributor.author | Wagen, Corin C | |
| dc.contributor.author | Ingoglia, Bryan Taylor | |
| dc.contributor.author | Buchwald, Stephen Leffler | |
| dc.date.accessioned | 2022-07-19T15:17:04Z | |
| dc.date.available | 2021-09-20T18:22:10Z | |
| dc.date.available | 2022-07-19T15:17:04Z | |
| dc.date.issued | 2019 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/132390.2 | |
| dc.description.abstract | © 2019 American Chemical Society. A rearrangement reaction of biarylphosphine-supported Pd(II) complexes was employed to synthesize 1,3,5-triaryl 2,4,6-triisopropylbenzene compounds, a class of molecules that has not previously been reported. The strain of the central hexasubstituted ring was investigated via X-ray crystallography. | en_US |
| dc.language.iso | en | |
| dc.publisher | American Chemical Society (ACS) | en_US |
| dc.relation.isversionof | 10.1021/ACS.JOC.9B02091 | en_US |
| dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
| dc.source | PMC | en_US |
| dc.title | Unexpected Formation of Hexasubstituted Arenes through a 2-fold Palladium-Mediated Ligand Arylation | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.relation.journal | Journal of Organic Chemistry | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2020-10-19T14:33:09Z | |
| dspace.orderedauthors | Wagen, CC; Ingoglia, BT; Buchwald, SL | en_US |
| dspace.date.submission | 2020-10-19T14:33:12Z | |
| mit.journal.volume | 84 | en_US |
| mit.journal.issue | 19 | en_US |
| mit.license | PUBLISHER_POLICY | |
| mit.metadata.status | Publication Information Needed | en_US |
