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dc.contributor.authorBuchwald, Stephen Leffler
dc.contributor.authorSenecal, Todd D.
dc.contributor.authorParsons, Andrew
dc.date.accessioned2012-08-02T18:42:27Z
dc.date.available2012-08-02T18:42:27Z
dc.date.issued2011-01
dc.date.submitted2010-11
dc.identifier.issn0022-3263
dc.identifier.issn1520-6904
dc.identifier.urihttp://hdl.handle.net/1721.1/71959
dc.description.abstractA method for the room temperature copper-mediated trifluoromethylation of aryl and heteroaryl boronic acids has been developed. This protocol is amenable to normal benchtop setup and reactions typically require only 1−4 h. Proceeding under mild conditions, the method tolerates a range of functional groups, allowing access to a variety of trifluoromethylarenes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant no. GM-46059)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant no. 1F32GM093532)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant no. CHE-9808061)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant no. DBI-9729592)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jo1023377en_US
dc.rightsArticle 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.sourcePMCen_US
dc.titleRoom Temperature Aryl Trifluoromethylation via Copper- Mediated Oxidative Cross-Couplingen_US
dc.typeArticleen_US
dc.identifier.citationBuchwald, Stephen Leffler, Andrew T. Parsons, and Todd D. Senecal. "Room Temperature Aryl Trifluoromethylation via Copper-Mediated Oxidative Cross-Coupling." The Journal of Organic Chemistry 76.4 (2011): 1174-1176.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.approverBuchwald, Stephen L.
dc.contributor.mitauthorBuchwald, Stephen Leffler
dc.contributor.mitauthorSenecal, Todd D.
dc.contributor.mitauthorParsons, Andrew
dc.relation.journalJournal of Organic Chemistryen_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.orderedauthorsSenecal, Todd D.; Parsons, Andrew T.; Buchwald, Stephen L.en
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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