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dc.contributor.authorShinde, Anand H.
dc.contributor.authorThomas, Annu Anna
dc.contributor.authorMague, Joel T.
dc.contributor.authorSathyamoorthi, Shyam
dc.date.accessioned2023-06-01T14:46:32Z
dc.date.available2023-06-01T14:46:32Z
dc.date.issued2021-10-19
dc.identifier.citationShinde, A. H., Thomas, A. A., Mague, J. T., & Sathyamoorthi, S. (2021). Highly Regio- and Diastereoselective Tethered Aza-Wacker Cyclizations of Alkenyl Phosphoramidates. The Journal of organic chemistry, 86(21), 14732–14758. https://doi.org/10.1021/acs.joc.1c01483en_US
dc.identifier.urihttps://hdl.handle.net/1808/34263
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic Chemistry, copyright © 2021 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.joc.1c01483.en_US
dc.description.abstractWe present highly diastereoselective tethered aza-Wacker cyclization reactions of alkenyl phosphoramidates. “Arming” the phosphoramidate tether with 5-chloro-8-quinolinol was essential to achieving >20:1 diastereoselectivity in these reactions. The substrate scope with respect to alkenyl alcohols and phosphoramidate tether was extensively explored. The scalability of the oxidative cyclization was demonstrated, and the product cyclophosphoramidates were shown to be valuable synthons, including for tether removal. With chiral alkenyl precursors, enantiopure cyclic phosphoramidates were formed.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2021 American Chemical Societyen_US
dc.titleHighly Regio- and Diastereoselective Tethered Aza-Wacker Cyclizations of Alkenyl Phosphoramidatesen_US
dc.typeArticleen_US
kusw.kuauthorShinde, Anand H.
kusw.kuauthorThomas, Annu Anna
kusw.kuauthorSathyamoorthi, Shyam
kusw.kudepartmentMedicinal Chemistryen_US
dc.identifier.doi10.1021/acs.joc.1c01483en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1966-8505en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4705-7349en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC10119688en_US
dc.rights.accessrightsopenAccessen_US


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