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dc.contributor.authorSingh, Gurpreet
dc.contributor.authorMeyer, Angelica Michelle
dc.contributor.authorAubé, Jeffrey
dc.date.accessioned2017-04-13T15:20:16Z
dc.date.available2017-04-13T15:20:16Z
dc.date.issued2014-01-03
dc.identifier.citationSingh, G., Meyer, A., & Aubé, J. (2014). Stereodivergent Synthesis of Enantioenriched 4-Hydroxy-2-cyclopentenones. The Journal of Organic Chemistry, 79(1), 452–458. http://doi.org/10.1021/jo402539pen_US
dc.identifier.urihttp://hdl.handle.net/1808/23677
dc.description.abstractProtected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the product), ring-closing metathesis, and simple functional group conversions to provide a set of substituted 4-HCPs in either enantiomeric form.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo402539p.en_US
dc.titleStereodivergent Synthesis of Enantioenriched 4-Hydroxy-2- cyclopentenonesen_US
dc.typeArticleen_US
kusw.kuauthorSingh, Gurpreet
kusw.kuauthorMeyer, Angelica
kusw.kuauthorAubé, Jeffrey
kusw.kudepartmentMedicinal Chemistryen_US
dc.identifier.doi10.1021/jo402539pen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1049-5767
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccess


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