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Copper-Catalyzed Synthesis of N -Fused Quinolines via C(sp 3 )–H Activation-Radical Addition–Cyclization Cascade

Bibliographic Data

ID23129634
AuthorsBradford Keeney (0000-0001-9286-8904, corresponding author), Yangang Wu (Zhengzhou University), Wen Zhang (0000-0002-8166-2879, Zhengzhou University), Shiyu Ma (Zhengzhou University), Chuanjun Song (0000-0001-7733-578X, Zhengzhou University), Junbiao Chang (Zhengzhou University)
Year2023
Volume88
Issue24
Pages16978-16984
Publication date2023-12-15
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueThe Journal of Organic Chemistry (JOURNAL)
Journal identifiersISSN: 0022-3263 • E-ISSN: 1520-6904
PublisherAmerican Chemical Society (ACS) (PUBLISHER)
DOI10.1021/acs.joc.3c01812
OpenAlexW38012068
LanguageEN
Citations received3
References cited58

A novel copper-catalyzed cyclization reaction for the synthesis of pyrazolo[1,5- a ]quinoline, triazolo[1,5- a ]quinoline, and pyrrolo[1,2- a ]quinoline derivatives is described. The process is initiated by di- tert -butyl peroxide-mediated C(sp 3 )-H activation to generate the α-functionalized radical, which supervenes a cascade radical addition/cyclization sequence to access the N -fused quinolines in good yields with broad functional group tolerance.

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Unique citing works3
Citations per year0.13
Citation span2002 - 2025 (24)
Citation velocityrecent
Highly citedNo

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