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dc.contributor.authorPotrząsaj, Aleksandra
dc.contributor.authorOciepa, Michał
dc.contributor.authorChaładaj, Wojciech
dc.contributor.authorGryko, Dorota
dc.date.accessioned2022-06-23T09:45:59Z
dc.date.available2022-06-23T09:45:59Z
dc.date.issued2022-03-25
dc.identifier.citationOrg. Lett. 2022, 24, 2469−2473. https://doi.org/10.1021/acs.orglett.2c00355en
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.other10.1021/acs.orglett.2c00355
dc.identifier.urihttps://depot.ceon.pl/handle/123456789/21367
dc.description.abstractOxetanes are valuable building blocks due to their well-explored propensity to undergo ring-opening reactions with nucleophiles. However, their application as precursors of radical species is still elusive. Herein, we present a bioinspired cobalt catalysis-based strategy to access unprecedented modes of radical reactivity via oxetane ring-opening. This powerful approach gives access to nucleophilic radicals that engage in reactions with SOMOphiles and low-valent transition metals. Importantly, the regioselectivity of these processes complements known methodologies.en
dc.description.sponsorshipNational Science Foundation (MAESTRO UMO-2020/38/A/ST4/00185) Foundation for Polish Sciences (FNP TEAM POIR.04.04.00−00−4232/17−00; START 64.2020) Wrocław Centre for Networking and Supercomputing (http://wcss.pl), grant No. 518.
dc.language.isoen
dc.publisherAmerican Chemical Societyen
dc.rightsCreative Commons Uznanie autorstwa 4.0*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/legalcode*
dc.subjectalkylsen
dc.subjectchemical reactionsen
dc.subjectethersen
dc.subjectorganic compoundsen
dc.subjectring opening reactionsen
dc.titleBioinspired Cobalt-Catalysis Enables Generation of Nucleophilic Radicals from Oxetanesen
dc.typearticleen
dc.contributor.organizationInstitute of Organic Chemistry, Polish Academy of Sciencesen


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