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dc.contributor.authorErnst, Johannes B.
dc.contributor.authorTay, Nicholas E. S.
dc.contributor.authorJui, Nathan T.
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2015-11-03T12:44:13Z
dc.date.available2015-11-03T12:44:13Z
dc.date.issued2014-06
dc.date.submitted2014-05
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttp://hdl.handle.net/1721.1/99671
dc.description.abstractA direct method for the regioselective construction of benzimidazolones is reported wherein a single palladium catalyst is employed to couple monosubstituted urea substrates with differentially substituted 1,2-dihaloaromatic systems. In this method, the catalyst is able to promote a cascade of two discrete chemoselective C–N bond-forming processes that allows the highly selective and predictable formation of complex heterocycles from simple, readily available starting materials.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award GM58160)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award GM099817)en_US
dc.description.sponsorshipLanxess Corporationen_US
dc.description.sponsorshipMassachusetts Institute of Technology. Undergraduate Research Opportunities Programen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ol501531qen_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.sourceACSen_US
dc.titleRegioselective Synthesis of Benzimidazolones via Cascade C–N Coupling of Monosubstituted Ureasen_US
dc.typeArticleen_US
dc.identifier.citationErnst, Johannes B., Nicholas E. S. Tay, Nathan T. Jui, and Stephen L. Buchwald. “Regioselective Synthesis of Benzimidazolones via Cascade C–N Coupling of Monosubstituted Ureas.” Organic Letters 16, no. 14 (July 18, 2014): 3844–3846. © 2014 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorErnst, Johannes B.en_US
dc.contributor.mitauthorTay, Nicholas E. S.en_US
dc.contributor.mitauthorJui, Nathan T.en_US
dc.contributor.mitauthorBuchwald, Stephen Leffleren_US
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsErnst, Johannes B.; Tay, Nicholas E. S.; Jui, Nathan T.; Buchwald, Stephen L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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