| dc.contributor.author | Maiti, Debabrata | |
| dc.contributor.author | Fors, Brett P. | |
| dc.contributor.author | Henderson, Jaclyn L. | |
| dc.contributor.author | Nakamura, Yoshinori | |
| dc.contributor.author | Buchwald, Stephen Leffler | |
| dc.date.accessioned | 2015-02-11T16:19:07Z | |
| dc.date.available | 2015-02-11T16:19:07Z | |
| dc.date.issued | 2010-09 | |
| dc.date.submitted | 2010-06 | |
| dc.identifier.issn | 2041-6520 | |
| dc.identifier.issn | 2041-6539 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/94326 | |
| dc.description.abstract | We report our studies on the use of two catalyst systems, based on the ligands BrettPhos and RuPhos, which provide the widest scope for Pd-catalyzed C–N cross-coupling reactions to date. Often low catalyst loadings and short reaction times can be used with functionalized aryl and heteroaryl coupling partners. The reactions are highly robust and can be set up and performed without the use of a glovebox. These catalysts should find wide application in the synthesis of complex molecules including pharmaceuticals, natural products and functional materials. | en_US |
| dc.description.sponsorship | Amgen Inc. | en_US |
| dc.description.sponsorship | National Institutes of Health (U.S.) (Grant GM-58160) | en_US |
| dc.description.sponsorship | American Chemical Society | en_US |
| dc.description.sponsorship | Boehringer Ingelheim | en_US |
| dc.description.sponsorship | National Science Foundation (U.S.) (CHE 9808061) | en_US |
| dc.description.sponsorship | National Science Foundation (U.S.) (DBI 9729592) | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Royal Society of Chemistry, The | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1039/c0sc00330a | en_US |
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
| dc.source | PMC | en_US |
| dc.title | Palladium-catalyzed coupling of functionalized primary and secondary amines with aryl and heteroaryl halides: two ligands suffice in most cases | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Maiti, Debabrata, Brett P. Fors, Jaclyn L. Henderson, Yoshinori Nakamura, and Stephen L. Buchwald. “Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases.” Chemical Science 2, no. 1 (2011): 57. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.contributor.mitauthor | Maiti, Debabrata | en_US |
| dc.contributor.mitauthor | Fors, Brett P. | en_US |
| dc.contributor.mitauthor | Henderson, Jaclyn L. | en_US |
| dc.contributor.mitauthor | Nakamura, Yoshinori | en_US |
| dc.contributor.mitauthor | Buchwald, Stephen Leffler | en_US |
| dc.relation.journal | Chemical Science | 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 |
| dspace.orderedauthors | Maiti, Debabrata; Fors, Brett P.; Henderson, Jaclyn L.; Nakamura, Yoshinori; Buchwald, Stephen L. | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0003-3875-4775 | |
| mit.license | OPEN_ACCESS_POLICY | en_US |
| mit.metadata.status | Complete | |