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- W2032016058 abstract "6-Oxiranyl- and 3-oxiranyl-2-phenylquinoline-4-carboxylic acid diisopropylamides react with secondary amines and lithium amides to give (aminohydroxyethyl)quinolines but with opposite regioselectivities. Upon epoxidation of 3-formylquinoline 2 a ∼5:1 mixture of atropisomers is formed. This ratio is maintained upon epoxide ring-opening with amines in ethanol at reflux, but with lithium amides at room temperature a 1.3:1 ratio of isomers is obtained." @default.
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- W2032016058 date "2003-12-01" @default.
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- W2032016058 title "Ring opening reactions of quinoline substituted epoxides" @default.
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- W2032016058 doi "https://doi.org/10.1016/j.tetlet.2003.10.062" @default.
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