Access to isoindole-derived BODIPYs by an aminopalladation cascade

Literature Information

Publication Date 2023-11-13
DOI 10.1039/D3CC04913B
Impact Factor 6.222
Authors

Heinrich F. von Köller, Finn J. Geffers, Pedram Kalvani, Adrian Foraita, Patrick-Eric J. Loß, Burkhard Butschke, Peter G. Jones, Daniel B. Werz


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Abstract

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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