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- W2068741605 abstract "(-)-(R)-Pyrrolam A was prepared in five steps, 95% ee and 25% yield, from (R)-benzyl prolinate. Closure of the pyrrolidine ring was effected by a domino addition-Wittig alkenation reaction with ylide Ph3PCCO, immobilized on a polystyrene resin. An indolizidinone was obtained likewise from (R)-benzyl pipecolate. The reduction of 1-ketopyrrolizidinones and 1-ketoindolizidinones is described." @default.
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- W2068741605 date "2007-05-02" @default.
- W2068741605 modified "2023-10-17" @default.
- W2068741605 title "Short Syntheses of (-)-<b>(</b> <b><i>R</i></b> <b>)</b>-Pyrrolam A and (1<b><i>S</i></b>)-1-Hydroxyindolizidin-3-one" @default.
- W2068741605 doi "https://doi.org/10.1055/s-2007-966035" @default.
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