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dc.contributor.authorLeypold, Mario
dc.contributor.authorD’Angelo, Kyan A
dc.contributor.authorMovassaghi, Mohammad
dc.date.accessioned2022-03-10T20:13:13Z
dc.date.available2022-03-10T20:13:13Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/141143
dc.description.abstract© 2020 American Chemical Society The direct α-sulfidation of tertiary amides using sulfoxide reagents under electrophilic amide activation conditions is described. Employing convenient and readily available reagents, selective functionalization takes place to generate isolable sulfonium ions en route to α-sulfide amides. Mechanistic studies identified activated sulfoxides as promoters of the desired transformation and enabled the extension of the methodology from benzylic to aliphatic amide substrates.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACS.ORGLETT.0C03160en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceACSen_US
dc.titleChemoselective α-Sulfidation of Amides Using Sulfoxide Reagentsen_US
dc.typeArticleen_US
dc.identifier.citationLeypold, Mario, D’Angelo, Kyan A and Movassaghi, Mohammad. 2020. "Chemoselective α-Sulfidation of Amides Using Sulfoxide Reagents." Organic Letters, 22 (22).
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-03-10T19:46:18Z
dspace.orderedauthorsLeypold, M; D’Angelo, KA; Movassaghi, Men_US
dspace.date.submission2022-03-10T19:46:19Z
mit.journal.volume22en_US
mit.journal.issue22en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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