AI Article Synopsis

  • Transition metal-catalyzed reactions in water are gaining popularity due to benefits like cost efficiency, safety, and easier separation processes.
  • Such reactions enable modifications of biopolymers in biological conditions and allow the cooperative use of enzymes and metal catalysts in complex reactions.
  • The review discusses advancements in water-soluble phosphine ligands since 2009 and explores their use in enhancing transition metal catalysis in aqueous environments.

Article Abstract

Transition metal-catalyzed reactions in aqueous media are experiencing a constant increase in interest. In homogenous catalysis the use of water as a solvent offers advantages in cost, safety, the possibility of two-phase catalysis and simplified separation strategies. In the life sciences, transition metal catalysis in aqueous systems enables the ligation or modification of biopolymers in buffer systems or even in their cellular environment. In biocatalysis, aqueous systems allow the simultaneous use of enzymes and transition metal catalysts in cascade reactions. The use of water-soluble phosphine ligands still represents the most reliable and popular strategy for transferring metal catalysts into the aqueous phase. This review summarizes the recent advancements in this field since 2009 and describes current synthetic strategies for the preparation of hydrophilic phosphines and phosphites. In addition, recent applications of transition metal catalysis in aqueous solvents using these hydrophilic ligands are presented.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898532PMC
http://dx.doi.org/10.1002/adsc.202001278DOI Listing

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