Catalytic activity of recyclable resorcinarene-protected antibacterial Pd nanoparticles in C-C coupling reactions

Syntheses and Biological Activities of Calix[4]resorcinarene Derivatives Modified by Sulfonamides

“…The calix [4]resorcinarenes and their derivatives were tested for their biological activity based on their phenol structures (Tables 1 and 2). [30,31] From the change in the size of the circle of inhibition from compounds 1a − 1d, it can be seen that the longer the calix [4]resorcinarene R-chain, the better the inhibition effect on E. coli, but the effect on Staphylococcus aureus appears to be opposite to that of E. coli. Comparison of the circles of inhibition produced by compounds 2a − 2d reveals that the change of the R group has a much smaller in uence on its antimicrobial activity than that of the group modi ed at the C-2 position.…”

Thiacalix[4]arene functionalized gold nano-assembly for recognition of isoleucine in aqueous solution and its antioxidant study

“…Our group has reported synthesis of hydrazide derivatives of different calixarene platforms for the preparation of gold, silver and palladium nanoparticles [22][23][24][25][26][27][28][29][30] acids, peptides, proteins, and carbohydrate, like ultimate substrates in biological processes, by synthetic receptors is a topic of great concern from both a host-guest chemistry and analytical application point of view [31][32][33][34][35]. Naturally occurring amino acids have recently been the topic of abundant investigation due to the functional and structural prominence of such interactions in chemistry and biology.…”