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dc.contributor.authorAscic, Erhad
dc.contributor.authorBuchwald, Stephen Leffler
dc.date.accessioned2017-07-05T18:40:21Z
dc.date.available2017-07-05T18:40:21Z
dc.date.issued2015-03
dc.date.submitted2015-03
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttp://hdl.handle.net/1721.1/110473
dc.description.abstractA diastereo- and enantioselective CuH-catalyzed method for the preparation of highly functionalized indolines is reported. The mild reaction conditions and high degree of functional group compatibility as demonstrated with substrates bearing heterocycles, olefins, and substituted aromatic groups, renders this technique highly valuable for the synthesis of a variety of cis-2,3-disubstituted indolines in high yield and enantioeselectivity.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Award GM46059)en_US
dc.description.sponsorshipDanish Council for Independent Research (Postdoctoral Fellowship)en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jacs.5b02316en_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.titleHighly Diastereo- and Enantioselective CuH-Catalyzed Synthesis of 2,3-Disubstituted Indolinesen_US
dc.typeArticleen_US
dc.identifier.citationAscic, Erhad, and Stephen L. Buchwald. “Highly Diastereo- and Enantioselective CuH-Catalyzed Synthesis of 2,3-Disubstituted Indolines.” Journal of the American Chemical Society 137.14 (2015): 4666–4669. © 2015 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorAscic, Erhad
dc.contributor.mitauthorBuchwald, Stephen Leffler
dc.relation.journalJournal of the American Chemical Societyen_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.orderedauthorsAscic, Erhad; Buchwald, Stephen L.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3875-4775
mit.licensePUBLISHER_POLICYen_US


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