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September 16, 2025European Journal of Organic Chemistry2 citations

Oxygen Electrophile‐Enabled Nickel‐Catalyzed Carboalkoxylation of Biphenylene CC σ‐Bond

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TITakeru InoueKHKoji Hirano

Key Points

  • The method enables efficient carboalkoxylation, producing ring-opening difunctionalization products.
  • Utilizing acetal-based, electron-deficient peroxides facilitates challenging CO cross coupling with nickel.
  • This approach extends to related borylalkoxylation by substituting arylboronates with danB–Bpin.
  • The findings open avenues for new synthetic strategies in organic chemistry, particularly in conjugated systems.

Abstract

A nickel‐catalyzed carboalkoxylation of the biphenylene CC σ‐bond with arylboronates and peroxides has been developed to form the corresponding ring‐opening difunctionalization products. The key to success is the use of acetal‐based, electron‐deficient peroxides, which enable the otherwise challenging CO cross coupling with nickel catalysts even under thermal conditions. A similar nickel catalysis is applicable to a related borylalkoxylation by replacement of arylboronates with danB–Bpin.

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Cite This Study

Inoue et al. (2025) studied this question.

synapsesocial.com/papers/68d4538731b076d99fa58a9bhttps://doi.org/10.1002/ejoc.202500555
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