Direct functionalization of BODIPY dyes by oxidative nucleophilic hydrogen substitution at the 3- or 3,5-positions
Chemical Communications2010Vol. 46(27), pp. 4908–4908
Citations Over TimeTop 10% of 2010 papers
Abstract
BODIPY dyes are shown to be susceptible to oxidative nucleophilic substitution of the alpha-hydrogens, incorporating nitrogen and carbon nucleophiles in a single, high yielding step. The reaction is an excellent alternative to conventional functionalization of this popular fluorophore.
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