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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2024, том 34, выпуск 2, страницы 198–200 (Mi mendc81)

Communications

Synthesis of furo[2,3-c]quinolinones via intramolecular C(3)–H arylation of furan core under Pd/NHC-catalysis

K. E. Shepelenkoa, I. G. Gnatiuka, M. E. Minyaevb, V. M. Chernysheva

a Platov South-Russian State Polytechnic University, Novocherkassk, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: An efficient procedure for the preparation of furo[2,3-c]-quinolin-4(5H)-ones from 2-furoic acid N-(o-bromoaryl)- amides via selective intramolecular C(3)–H arylation of the furan nucleus involves the catalysis by a Pd/NHC system generated in situ from Pd(OAc)2 and readily available IPrSPh HCl proligand. A series of novel furo[2,3-c]quinolin-4(5H)-ones were prepared in 65–80% isolated yields.

Ключевые слова: palladium, C–H activation, arylation, N-heterocyclic carbene ligands, furo[2,3-c]quinolin-4(5H)-ones.

Язык публикации: английский

DOI: 10.1016/j.mencom.2024.02.012



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