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• W2511321336 abstract "A formal amide insertion reaction for the synthesis of nitrogen-bridged polycyclic frameworks with diverse functionalities was developed using a sustainable copper catalyst as an advantageous alternative to precious rhodium catalysts. The remarkable feature of this methodology is the amount of catalyst loading (0.05 mol%). The optimized reaction conditions enable access to aromatic ring-fused 8-azabicyclo[3.2.1]octane, 9-azabicyclo[3.3.1]nonane, and 6-azabicyclo[3.2.2]nonane derivatives in moderate to excellent yields." @default.
• W2511321336 created "2016-09-16" @default.
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• W2511321336 date "2016-08-31" @default.
• W2511321336 modified "2023-09-27" @default.
• W2511321336 title "Construction of Functionalized Azapolycyclic Architectures<i>via</i>Formal Amide Insertion at a Low Catalyst Loading of Copper Trifluoroacetylacetonate" @default.
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• W2511321336 doi "https://doi.org/10.1002/adsc.201600603" @default.
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