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- W3136126202 abstract "Abstract This work describes a study on the selective functionalization of norbornadiene across nitrile oxide 1,3‐dipolar cycloaddition/ring‐opening (ROM)/cross‐metathesis (CM) protocols. Readily available norbornadiene was transformed into novel bicyclic scaffolds with multiple chiral centers. The described syntheses involved selective cycloadditions followed by ring‐opening metathesis of the resulting cycloalkane‐fused isoxazoline derivatives, and selective cross‐metathesis by chemodiscrimination of the C=C bonds of the resulting alkenylated heterocycles. The cross‐metathesis transformations have been studied under various experimental conditions with the aim of exploring the substrate influence and chemodifferentiation of the olefin bonds providing the corresponding functionalized isoxazoline derivatives." @default.
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- W3136126202 date "2021-04-06" @default.
- W3136126202 modified "2023-09-23" @default.
- W3136126202 title "Selective Functionalization of Norbornadiene Through Nitrile Oxide Cycloaddition/Ring‐Opening/Cross‐Metathesis Protocols" @default.
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- W3136126202 doi "https://doi.org/10.1002/ajoc.202100147" @default.
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