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- W2896881185 abstract "Intramolecular oxidative amination of readily accessible aminocyclooct‐4‐enes provides rapid and regioselective access to the 9‐azabicyclo[4.2.1]nonane framework characteristic of the natural product anatoxin‐a (1). This has enabled the synthesis of sp 3 ‐rich chemical scaffolds suitable for diversification. A library of 881 lead‐like compounds is reported alongside a formal synthesis of anatoxin‐a (1)." @default.
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- W2896881185 date "2018-10-18" @default.
- W2896881185 modified "2023-09-26" @default.
- W2896881185 title "PdII -Mediated Oxidative Amination for Access to a 9-Azabicyclo[4.2.1]nonane Compound Library and Anatoxin-a" @default.
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- W2896881185 doi "https://doi.org/10.1002/ejoc.201801209" @default.
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