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Bringing stereoselectivity to C(sp3)–H nucleophilic fluorination

Research output: Contribution to journalComment/debate

Abstract

Reporting in Nature Catalysis , Yu and colleagues have achieved an enantioselective C(sp3)–H fluorination of amides by using Pd catalysis, chiral amino-acid-derived ligands, and nucleophilic fluoride sources.

Original languageEnglish
Article number101568
JournalChem Catalysis
Volume5
Issue number11
DOIs
StatePublished - Nov 20 2025

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