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May 18, 2026European Journal of Organic Chemistry2 citationsOpen Access

Achieving Diverse Functionalizations of Electron‐Deficient Aryl Halides via Carbonate‐Mediated Electron‐Donor–Acceptor Complexes

KSKrishnakumar SachidanandanCSCole StenftenagelAJAthul Joshy

Key Points

  • This research aims to develop a simple and cost-effective method for functionalizing electron-deficient aryl halides.
  • Utilized carbonate-mediated activation of aryl iodides and bromides.
  • Conducted various functional group transformations including arylation and dehalogenation.
  • Employed photo-induced approaches for activating molecular motifs.
  • Efficient arylation of electron-deficient aryl halides was achieved.
  • Successful dehalogenation and borylation of starting materials were observed.
  • The protocol demonstrated effectiveness without the need for expensive precious metal catalysts.

Abstract

Aryl halides are excellent precursors for functional group interconversion due to their malleability and diversity. They are also among the most common building blocks due to their use in cross‐coupling reactions. Traditional methodologies for activating these motifs make use of expensive precious metals, such as palladium, and often require the use of complex and even more expensive ligands. Electron‐donor–acceptor complexes have recently gained attention as a new photo‐induced approach for the activation of various molecular motifs, including aryl halides. Herein, further extension of these methodologies led to the development of a straightforward and simple protocol that uses inexpensive carbonate bases for the activation of electron‐deficient aryl iodides and bromides. The procedure was employed for the arylation, dehalogenation, deuteration, chalcogenation, and borylation of aryl halide starting materials.

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Cite This Study

Sachidanandan et al. (2026) studied this question.

synapsesocial.com/papers/6a0aac955ba8ef6d83b6ff4bhttps://doi.org/10.1002/ejoc.70519
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