4.8 Article

Vicarious Nucleophilic Substitution of α-Hydrogen of BODIPY and Its Extension to Direct Ethenylation

Journal

ORGANIC LETTERS
Volume 13, Issue 6, Pages 1470-1473

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol200148u

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Direct, oxidizer-free substitution of the 3-hydrogen of BODIPY derivatives has been established through a vicarious nucleophilic substitution procedure. This methodology has been combined with a reversible Michael addition on nitrostyrenes to provide a novel, highly efficient entry to the valuable 3-styrylated BODIPY dyes.

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