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dc.contributor.authorZhou, Yujing
dc.contributor.authorEngl, Oliver D.
dc.contributor.authorBandar, Jeffrey
dc.contributor.authorChant, Emma D.
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2020-07-08T18:50:03Z
dc.date.available2020-07-08T18:50:03Z
dc.date.issued2018-05
dc.identifier.issn0570-0833
dc.identifier.urihttps://hdl.handle.net/1721.1/126087
dc.description.abstractA CuH-catalyzed enantioselective hydroamidation reaction of vinylarenes has been developed using readily accessible 1,4,2-dioxazol-5-ones as electrophilic amidating reagents. This method provides a straightforward and efficient approach to synthesize chiral amides in good yields with high levels of enantiopurity under mild conditions. Moreover, this transformation tolerates substrates bearing a broad range of functional groups.en_US
dc.description.sponsorshipNational Institutes of Health (grant nos. GM58160 and GM122483)en_US
dc.language.isoen
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ANIE.201802797en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleCuH-Catalyzed Asymmetric Hydroamidation of Vinylarenesen_US
dc.typeArticleen_US
dc.identifier.citationZhou, Yujing, et al. "CuH-Catalyzed Asymmetric Hydroamidation of Vinylarenes." Angewandte Chemie International Edition 57, 22 (May 2018): p. 6672-75 doi 10.1002/ANIE.201802797 ©2018 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_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
dc.date.updated2019-12-12T19:07:59Z
dspace.date.submission2019-12-12T19:08:01Z
mit.journal.volume57en_US
mit.journal.issue22en_US
mit.metadata.statusComplete


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