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The ring-closing metathesis (RCM) reaction of N-vinyl-alpha-(2-styryl)azinium salts, using the Hoveyda-Grubbs catalyst, leads to different tricyclic and tetracyclic azonia cations with moderate to good yields. This is the first time that a highly electron-deficient alkene such as an N-vinylpyridinium has been involved in an RCM process.
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