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• W2053196694 abstract "The tin hydride-mediated aryl radical cyclization of a number of 4-(2′-bromo-N-methylanilino)methyl-1-alkylquinolin-2(1H)-ones under mild neutral condition afforded 1-alkyl-3,4-dihydroquinolin-2(1H)-one-4-spiro-3′-(1-methylindolines) in excellent yield. The starting materials, amines were derived from 4-bromomethyl-N-methyl quinolin-2(1H)-ones and 2-bromo-N-methyl anilines by refluxing in acetone in the presence of anhydrous potassium carbonate and sodium iodide (Finkelstein condition). J. Heterocyclic Chem., 46, 492 (2009)." @default.
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• W2053196694 date "2009-05-01" @default.
• W2053196694 modified "2023-09-27" @default.
• W2053196694 title "Regioselective synthesis of bioactive spiro heterocyclic compounds containing both indoline and quinolone moieties by aryl radical cyclization" @default.
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• W2053196694 doi "https://doi.org/10.1002/jhet.101" @default.
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