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Article: Manipulating alkoxy radicals for site- and enantioselective C–H oxidation

TitleManipulating alkoxy radicals for site- and enantioselective C–H oxidation
Authors
Issue Date13-Mar-2025
PublisherCell Press
Citation
Chem, 2025, v. 11, n. 3 How to Cite?
Abstract

Using C–H substrates as limiting reagents to achieve non-directed C–H activation with high selectivity has been a long-standing challenge in organic synthesis. Recently in Nature Catalysis, Liu et al. introduce a biomimetic catalytic system that employs Cu(II)-bound tert-butoxy radicals for site-selective C–H abstraction, enabling highly efficient asymmetric C(sp3)–H oxidation.


Persistent Identifierhttp://hdl.handle.net/10722/355259
ISSN
2023 SCImago Journal Rankings: 6.556

 

DC FieldValueLanguage
dc.contributor.authorHe, Jian-
dc.contributor.authorChe, Chi-Ming-
dc.date.accessioned2025-04-01T00:35:16Z-
dc.date.available2025-04-01T00:35:16Z-
dc.date.issued2025-03-13-
dc.identifier.citationChem, 2025, v. 11, n. 3-
dc.identifier.issn2451-9308-
dc.identifier.urihttp://hdl.handle.net/10722/355259-
dc.description.abstract<p>Using C–H substrates as limiting reagents to achieve non-directed C–H activation with high selectivity has been a long-standing challenge in organic synthesis. Recently in <em>Nature Catalysis</em>, Liu et al. introduce a biomimetic catalytic system that employs Cu(II)-bound <em>tert</em>-butoxy radicals for site-selective C–H abstraction, enabling highly efficient asymmetric C(sp<sup>3</sup>)–H oxidation.</p>-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofChem-
dc.titleManipulating alkoxy radicals for site- and enantioselective C–H oxidation-
dc.typeArticle-
dc.identifier.doi10.1016/j.chempr.2025.102495-
dc.identifier.scopuseid_2-s2.0-86000511302-
dc.identifier.volume11-
dc.identifier.issue3-
dc.identifier.eissn2451-9294-
dc.identifier.issnl2451-9294-

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