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Fluoride-activated silicon catalysis enables C(sp 3 )–H amination of cyclic benzylic ethers and amines using chloramine-T

Year: 2026

Type: article

Abstract: Fluoride-activated silicon catalysis enables transition-metal-free radical benzylic C(sp 3 )–H amination of cyclic benzylic ethers and amines using bench-stable chloramine-T as the nitrogen source.

Source: Chemical Science

DOI: 10.1039/d6sc06229f

Authors: Geun Ho Kim, Huimyoung Byeon, Dong Wan Kim, Dae Won Kim, Jung Woon Yang

Institution: Sungkyunkwan University

Language: English

Topic: Radical Photochemical Reactions

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

Open Access status: diamond

Funders: Ministry of Education, Korea Basic Science Institute, National Research Foundation of Korea, Ministry of Science and ICT, South Korea

Awards: G1032476353, G1336057942, G3812690899, G4286615259, G4541009143, G4646548868, G6473233090, G7781397566

OpenAlex ID: W7213541854

FWCI:

Cites: 57

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Related to: 10