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- W2750583009 abstract "Abstract The first enantioselective total synthesis of (−)‐deoxoapodine is described. Our synthesis of this hexacyclic aspidosperma alkaloid includes an efficient molybdenum‐catalyzed enantioselective ring‐closing metathesis reaction for the desymmetrization of an advanced intermediate that introduces the C5‐quaternary stereocenter. After C21‐oxygenation, the pentacyclic core was accessed by electrophilic C19‐amide activation and transannular spirocyclization. A biogenetically inspired dehydrative C6‐etherification reaction proved highly effective to secure the F‐ring and the fourth contiguous stereocenter of (−)‐deoxoapodine with complete stereochemical control." @default.
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- W2750583009 date "2017-09-27" @default.
- W2750583009 modified "2023-10-16" @default.
- W2750583009 title "Enantioselective Total Synthesis of (−)-Deoxoapodine" @default.
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- W2750583009 doi "https://doi.org/10.1002/anie.201708088" @default.
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