Discovering efficient methods for the formation of carbon-carbon bonds is a central ongoing theme in organic synthesis. Cross-coupling reactions catalysed by metal nanoparticles are attractive alternatives to the traditional use of metal counterparts due to the catalytic tunability, selectivity, recyclability and reusability of the nanoparticles. The ongoing search for sustainable processes demands that reusable and environmentally benign catalysts are used. While the advantages of nanoparticles catalysts over bulk catalysts cannot be overemphasised, the problem of sintering, agglomeration and leaching are drawbacks to their full industrial applications. Hence, efforts are being made towards advancing the efficiency of the catalytic nanoparticle systems over the years. This review presents the progress, the challenges and the prospects of palladium nanoparticle with focus on Heck, Suzuki, Hiyama and Sonogashira cross-coupling reactions involving (hetero) aryl halides and the analogues.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015734PMC
http://dx.doi.org/10.1002/open.202000309DOI Listing

Publication Analysis

Top Keywords

halides analogues
8
cross-coupling reactions
8
prospects applications
4
applications palladium
4
nanoparticles
4
palladium nanoparticles
4
nanoparticles cross-coupling
4
cross-coupling heteroaryl
4
heteroaryl halides
4
analogues discovering
4

Similar Publications

CFH-synthon enables asymmetric radical difluoroalkylation for synthesis of chiral difluoromethylated amines.

Nat Commun

January 2025

Department of Pharmacy, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.

The difluoromethyl group is a crucial fluorinated moiety with distinctive biological properties, and the synthesis of chiral CF₂H-containing analogs has been recognized as a powerful strategy in drug design. To date, the most established method for accessing enantioenriched difluoromethyl compounds involves the enantioselective functionalization of nucleophilic and electrophilic CF₂H synthons. However, this approach is limited by lower reactivity and reduced enantioselectivity.

View Article and Find Full Text PDF

Antimicrobial Activity and Mode of Action of N-Heterocyclic Carbene Silver(I) Complexes.

Molecules

December 2024

Department of Pharmacy and Interuniversity Research Centre on Bioactive Peptides (CIRPeB), University of Naples "Federico II", Via Montesano 49, 80131 Naples, Italy.

Silver drugs have played a vital role in human healthcare for the treatment of infections for many centuries. Currently, due to antibiotic resistance, a potential scenario or the application of silver complexes may arise as substitutes for conventional antibiotics. In this perspective, N-heterocyclic carbene (NHC) ligands have been selected as carrier molecules for silver ions.

View Article and Find Full Text PDF

The title compound is a germanium-based hybrid metal halide that represents a less-toxic alternative to more popular lead-based analogues in optoelectronic applications. {(2-ICHNH)[GeI]} is composed of infinite inorganic layers that are formed by [GeI] octa-hedra connected in a corner-sharing manner with four equatorial I atoms. The organic (2-ICHNH) cations inter-leave the inorganic layers.

View Article and Find Full Text PDF
Article Synopsis
  • A cationic N-heterocyclic phosphenium iron tetracarbonyl complex was synthesized and its reactivity with various anionic reactants was investigated, resulting in different products depending on the anion involved.
  • Reactions with fluoride and chloride produced neutral diazaphospholenes, while bromide and iodide led to NHP iron halides through metal addition and decarbonylation.
  • At room temperature, the cationic complex primarily reduced to form a detectable Fe-centered radical, whereas at -78 °C, CH-metalation was favored, further evidenced by the characterization of a neutral borane-adduct.
  • The complex’s reactivity variations are attributed to its higher electrophilicity compared to neutral complexes
View Article and Find Full Text PDF

Defluorinative Cyclization of Enamides with Fluoroalkyl Halides Through Two Vicinal C(sp)─F Bonds Functionalization.

Adv Sci (Weinh)

December 2024

Technical Institute of Fluorochemistry, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing, 211816, China.

Introducing distinctive functional groups to expand the structural diversity and improve the intrinsic properties of parent molecules has been an essential pursuit in organic chemistry. By using perfluoroalkyl halide (PFAH) as a nontraditional, readily available, ideal 1,2-difluoroalkenyl coupling partner, a defluorinative cyclization reaction of enamides for the construction of fluoroalkenyl oxazoles is first developed. The selective and controllable two-fold cleavage of vicinal C(sp)─F bonds in PFAH not only enables the introduction of a specific 1,2-difluoroalkenyl moiety with ease but also results in the functionalization of two C(sp)─H bonds of enamides without the need for metal catalyst, photocatalyst, oxidant, or light.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!