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dc.contributor.authorShinde, Anand H.
dc.contributor.authorNagamalla, Someshwar
dc.contributor.authorSathyamoorthi, Shyam
dc.date.accessioned2023-06-13T15:38:56Z
dc.date.available2023-06-13T15:38:56Z
dc.date.issued2020-05-17
dc.identifier.citationShinde, A.H., Nagamalla, S. & Sathyamoorthi, S. N-arylated oxathiazinane heterocycles are convenient synthons for 1,3-amino ethers and 1,3-amino thioethers. Med Chem Res 29, 1223–1229 (2020). https://doi.org/10.1007/s00044-020-02556-xen_US
dc.identifier.urihttps://hdl.handle.net/1808/34348
dc.description.abstractThis communication describes a variety of nucleophilic ring openings of N-arylated oxathiazinane heterocycles. We find that this reaction is compatible with phenoxides, naphthoxides, and thiolates and allows for the rapid assembly of N-aryl-amino ethers and N-aryl-amino thioethers. Fourteen examples are shown and a mechanistic pathway is hypothesized.en_US
dc.publisherSpringeren_US
dc.rightsCopyright © 2020, Springer Science Business Media, LLC, part of Springer Nature.en_US
dc.subjectNucleophileen_US
dc.subjectSulfamateen_US
dc.subjectOxathiazinaneen_US
dc.subjectAza-Wackeren_US
dc.titleN-arylated oxathiazinane heterocycles are convenient synthons for 1,3-amino ethers and 1,3-amino thioethersen_US
dc.typeArticleen_US
kusw.kuauthorShinde, Anand H.
kusw.kuauthorNagamalla, Someshwar
kusw.kuauthorSathyamoorthi, Shyam
kusw.kudepartmentMedicinal Chemistryen_US
dc.identifier.doi10.1007/s00044-020-02556-xen_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.pmidPMC10191371en_US
dc.rights.accessrightsopenAccessen_US


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