Efficient Synthesis of Amino Lactones via Copper-catalysed Alkene Aminooxygenation

dc.contributor.authorCasciotti, Martina
dc.contributor.authorPérez Romero, Pedro José
dc.contributor.authorRodríguez Belderraín, Tomás
dc.contributor.authorMuñoz Molina, José María
dc.contributor.authorCasciotti
dc.date.accessioned2026-01-07T11:41:12Z
dc.date.available2026-01-07T11:41:12Z
dc.date.issued2025-04-14
dc.description.abstractThe synthesis of 5–7 membered oxygenated heterocycles by intramolecular aminooxygenation of unsaturated alkenes using commercially available N-fluorobenzenesulfonimide as amination reagent and TpiPr2Cu(NCCH3) as precatalyst is reported. With unsaturated aliphatic carboxylic acids, the corresponding lactones are obtained from moderate to almost quantitative yields employing a catalyst loading of 2.5 mol% under mild conditions, whereas 2-vinylbenzoic acids originate lower yields.
dc.description.centerCIQSO
dc.description.departmentQuímica "Profesor José Carlos Vílchez Martín"
dc.identifier.citationCasciotti, M., Muñoz-Molina, J. M., Belderrain, T., & Perez, P. J. (2025). Efficient Synthesis of Amino Lactones via Copper‐catalysed Alkene Aminooxygenation. Advanced Synthesis & Catalysis, 367(11). https://doi.org/10.1002/adsc.202500062
dc.identifier.doi10.1002/adsc.202500062
dc.identifier.urihttps://hdl.handle.net/10272/27605
dc.language.isoeng
dc.publisherWiley
dc.relation.projectIDPID2020-113797RB-C21), P18-1536-RT, P20-00348, UHU202053
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.otherAmination
dc.subject.otherCopper catalysis
dc.subject.otherRadical reactions
dc.subject.otherLactones
dc.subject.otherC-N bond formation
dc.titleEfficient Synthesis of Amino Lactones via Copper-catalysed Alkene Aminooxygenation
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
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relation.isAuthorOfPublication8e141a40-1260-4c0a-a95d-0ef4e63b8aad
relation.isAuthorOfPublication.latestForDiscoveryc6f8222a-d8d2-4736-baa6-4a2330bdf6b6

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