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• W3005802148 abstract "Abstract Three-component reactions of monoalkyl malonates, cyanoacetic acids or 2-ketocarboxylic acids, N-methylglycine, and formaldehyde were developed to rapidly access 3-substituted pyrrolidines in 17–97% yield. These reactions represent a double decarboxylative domino-sequence promoted by pyrrolidine and involve N-methylazomethine ylide as the reactive intermediate." @default.
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• W3005802148 date "2020-04-01" @default.
• W3005802148 modified "2023-09-24" @default.
• W3005802148 title "Double decarboxylative route to 3-substituted pyrrolidines: Reaction of monoalkyl malonates and related carboxylic acids with sarcosine and formaldehyde" @default.
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• W3005802148 doi "https://doi.org/10.1016/j.tetlet.2020.151727" @default.
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