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Covalent Tethers for Precise Amino Alcohol Syntheses: Ring Opening of Epoxides by Pendant Sulfamates and Sulfamides
dc.contributor.author | Nagamalla, Someshwar | |
dc.contributor.author | Mague, Joel T. | |
dc.contributor.author | Sathyamoorthi, Shyam | |
dc.date.accessioned | 2023-06-13T20:54:06Z | |
dc.date.available | 2023-06-13T20:54:06Z | |
dc.date.issued | 2023-02-06 | |
dc.identifier.citation | Nagamalla, S., Mague, J. T., & Sathyamoorthi, S. (2023). Covalent Tethers for Precise Amino Alcohol Syntheses: Ring Opening of Epoxides by Pendant Sulfamates and Sulfamides. Organic letters, 25(6), 982–986. https://doi.org/10.1021/acs.orglett.3c00053 | en_US |
dc.identifier.uri | https://hdl.handle.net/1808/34375 | |
dc.description | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, Copyright © 2023 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.orglett.3c00053. | en_US |
dc.description.abstract | We describe the development of the first ring opening of epoxides using pendant sulfamates and sulfamides. These reactions are promoted by a base and proceed under mild conditions to afford oxathiazinanes and cyclic sulfamides with excellent diastereoselectivity and regiocontrol. The reactions scale well, and the products serve as synthons for ring-opening reactions. | en_US |
dc.publisher | American Chemical Society | en_US |
dc.rights | Copyright © 2023 American Chemical Society | en_US |
dc.subject | Cyclization | en_US |
dc.subject | Ethers | en_US |
dc.subject | Mixtures | en_US |
dc.subject | Ring opening reactions | en_US |
dc.subject | Substitution reactions | en_US |
dc.title | Covalent Tethers for Precise Amino Alcohol Syntheses: Ring Opening of Epoxides by Pendant Sulfamates and Sulfamides | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Nagamalla, Someshwar | |
kusw.kuauthor | Sathyamoorthi, Shyam | |
kusw.kudepartment | Medicinal Chemistry | en_US |
dc.identifier.doi | 10.1021/acs.orglett.3c00053 | en_US |
dc.identifier.orcid | https://orcid.org/0000-0003-4705-7349 | en_US |
kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC10017054 | en_US |
dc.rights.accessrights | embargoedAccess | en_US |