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Cross‐Coupling Reactions in Aqueous Micellar Media

  • Alexander Uner
  • , Liam T. Ball*
  • *Corresponding author for this work

Research output: Contribution to journalReview article (Academic Journal)peer-review

10 Citations (Scopus)

Abstract

Thanks to their ability to efficiently and reliably construct carbon–carbon and carbon–heteroatom bonds, cross‐coupling reactions remain at the forefront of chemical research in both academic and industrial settings. However, the growing emphasis on sustainability has exposed the shortcomings of cross‐coupling chemistry in several areas, including the preponderance toward toxic polar aprotic solvents, high loadings of precious metal catalysts, and production of large quantities of waste. In recent years, micellar reaction media, formed by dissolution of surfactant molecules in water, have emerged as a sustainable alternative to organic solvents, allowing for use of water as the bulk medium while circumventing the usual solubility issues associated with its use. This Review introduces the fundamentals of surfactants for synthesis and summarizes recent advances in cross‐coupling chemistry in micellar media, with a focus on improving both sustainability and reaction performance using micellar technologies.
Original languageEnglish
Article numbere202500499
JournalEuropean Journal of Organic Chemistry
Volume28
Issue number33
Early online date17 Jun 2025
DOIs
Publication statusE-pub ahead of print - 17 Jun 2025

Bibliographical note

Publisher Copyright:
© 2025 The Author(s). European Journal of Organic Chemistry published by Wiley-VCH GmbH.

Research Groups and Themes

  • Organic & Biological

Keywords

  • cross‐coupling
  • micellar media
  • surfactants
  • sustainability
  • homogeneous catalysis

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