Use of <i>F</i>-BODIPYs as a Protection Strategy for Dipyrrins: Optimization of BF₂ Removal

We recently reported the first general method for the deprotection of 4,4-difluoro-4-bora-3a,4a-diaza-<i>s</i>-indacenes (<i>F</i>-BODIPYs) involving a microwave-assisted procedure for the removal of the BF₂ moiety, and liberation of the corresponding free-base dipyrrin. Further optimization of the reaction has resulted in a more convenient and accessible protocol. The availability of this new methodology enables BF₂-complexation to be used as a dipyrrin protection strategy. Herein lies a detailed examination of the deprotection reaction, with a view to optimization and gaining mechanistic insight, and its application in facilitating a multistep synthesis of pyrrolyldipyrrins.