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dc.contributor.authorUeda, Satoshi
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2013-11-04T15:33:22Z
dc.date.available2013-11-04T15:33:22Z
dc.date.issued2012-09
dc.date.submitted2012-06
dc.identifier.issn14337851
dc.identifier.issn1521-3773
dc.identifier.urihttp://hdl.handle.net/1721.1/81968
dc.description.abstractWhat N would you like? The chemoselective and complementary Pd- and Cu-catalyzed N-arylation of 2-aminobenzimidazoles is described. Selective N-arylation of the amino group was achieved with a Pd-catalyzed method, while selective N-arylation of azole nitrogen was achieved with a Cu-catalyzed procedure (see scheme).en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (GM58160)en_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/anie.201204710en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleCatalyst-Controlled Chemoselective Arylation of 2-Aminobenzimidazolesen_US
dc.typeArticleen_US
dc.identifier.citationUeda, Satoshi, and Stephen L. Buchwald. “Catalyst-Controlled Chemoselective Arylation of 2-Aminobenzimidazoles.” Angewandte Chemie International Edition 51, no. 41 (October 8, 2012): 10364-10367.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorUeda, Satoshien_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.relation.journalAngewandte Chemie International Editionen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsUeda, Satoshi; Buchwald, Stephen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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