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- W2222751582 endingPage "2194" @default.
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- W2222751582 abstract "Abstract Two amino acids play a key role in the first total synthesis of lycopalhine A. l ‐glutamic acid serves as a convenient chiral starting material for the 13‐step synthesis, and l ‐proline promotes an unusual 5‐ endo ‐trig Mannich cyclization that generates the central pyrrolidine ring of the Lycopodium alkaloid. The bicyclo[3.3.0]octanol moiety of the molecule is formed through an intramolecular aldol addition that may occur spontaneously in nature." @default.
- W2222751582 created "2016-06-24" @default.
- W2222751582 creator A5009831581 @default.
- W2222751582 creator A5042433434 @default.
- W2222751582 date "2016-01-08" @default.
- W2222751582 modified "2023-10-13" @default.
- W2222751582 title "Expedient Synthesis of (+)-Lycopalhine A" @default.
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- W2222751582 doi "https://doi.org/10.1002/anie.201509602" @default.
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