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- W2460295132 abstract "Spiroanthraceneoxazolidine reacts with diethyl 2-arylcyclopropane-1,1-dicarboxylates at 140–200 °C in the presence of magnesium bromide diethyl etherate to give 5-arylpyrrolidine-3,3-dicarboxylates. Yield and ease of the reaction were well correlated with the electron-donating nature of the aryl(heteroaryl) substituent at the cyclopropane ring. This one-pot domino reaction allows the formation of a number of functionalized arylpyrrolidines in 16–54% yields." @default.
- W2460295132 created "2016-07-22" @default.
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- W2460295132 date "2016-08-01" @default.
- W2460295132 modified "2023-10-09" @default.
- W2460295132 title "Spiroanthraceneoxazolidine as a synthetic equivalent of methanimine in the reaction with donor–acceptor cyclopropanes. Synthesis of diethyl 5-arylpyrrolidine-3,3-dicarboxylates" @default.
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- W2460295132 doi "https://doi.org/10.1016/j.tetlet.2016.07.007" @default.
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