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Carbonylation as a Key Step in New Tandem Reactions - A Route to BODIPYs.

Lukas MillerAlba ImpelmannFelix BauerBernhard Breit
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2024)
Herein, a highly efficient five-step reaction sequence to BODIPYs is presented. The key step is the combination of transition metal-catalyzed in-situ generation of aldehydes and their subsequent organocatalytic activation to yield dipyrromethanes, which are further converted to the corresponding BODIPY. Classic syntheses towards BODIPYs have relied on aldehydes or acid chlorides, which are often not commercially available and rather sensitive to handle. The presented approach starts from readily available and stable alkenes or aryl-bromides, which allows to extend the range of readily available BODIPYs that can be tailored for their specific use. The synthesis of 55 derivatives with overall yields of up to 78 % demonstrates the wide applicability and advantages of the presented method.
Keyphrases
  • highly efficient
  • transition metal
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