Access to isoindole-derived BODIPYs by an aminopalladation cascade
Literature Information
Heinrich F. von Köller, Finn J. Geffers, Pedram Kalvani, Adrian Foraita, Patrick-Eric J. Loß, Burkhard Butschke, Peter G. Jones, Daniel B. Werz
Here, we present a new route to dyes of the BODIPY family. We first built up a N-Boc-protected dipyrromethene scaffold via an aminopalladation cascade. Subsequentially, the pyrrole moiety was deprotected and the BF2 unit inserted. Depending on the terminating reaction, BODIPYs with either aryl or alkynyl moieties were accessible.
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