A simple and efficient procedure for Suzuki coupling of aryl bromides/iodides with aryl- and alkylboronic acids catalyzed by in situ-generated palladium(0) nanoparticles in water without any ligand in open air to produce a variety of functionalized biaryls and alkyl-aryls has been developed. The boronic acids act here as the reducing agent for the formation of Pd nanoparticles. The reactions are remarkably fast (5 min) and high yielding. The catalyst is recyclable up to three runs without loss of efficiency
A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simpl...
The metal accumulating ability of plants has previously been used to capture metal contaminants from...
Glucose stabilized palladium nanoparticles (PdNPs) have been prepared and the application of NPs in ...
InIn this work, it was investigated to use of poly(N-ethyl-4-vinylpyridinium) bromide stabilized pal...
A simple and efficient protocol is described for a Suzuki reaction catalyzed by poly(vinyl chloride)...
Herein we report the use of zeolite confined palladium(0) nanoclusters as efficient and recyclable c...
Highly selective carbonylative Suzuki reactions of aryl iodides with arylboronic acids using an in s...
Palladium nanoparticles are a valuable alternative to molecular catalysts for not requiring costly a...
Suzuki couplings of aryl bromides were efficiently performed by a polymer supported palladium cataly...
Palladium(0) nanoclusters stabilized by poly(4-styrenesulfonic acid-co-maleic acid), PSSA-co-MA, wer...
Highly dispersed poly(amic acid) salt-stabilised palladium nanoparticles(PdNPs/PAAS) were synthesise...
The first example of Pd-catalyzed Suzuki cross-coupling of readily available arylhydrazines with ary...
The results of a ligand-free Pd(OAc)(2)-catalyzed Suzuki-Miyaura C-C coupling performed at room temp...
The metal accumulating ability of plants has previously been used to capture metal contaminants from...
A facile surfactant mediated Heck and Suzuki coupling procedure in water has been developed using li...
A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simpl...
The metal accumulating ability of plants has previously been used to capture metal contaminants from...
Glucose stabilized palladium nanoparticles (PdNPs) have been prepared and the application of NPs in ...
InIn this work, it was investigated to use of poly(N-ethyl-4-vinylpyridinium) bromide stabilized pal...
A simple and efficient protocol is described for a Suzuki reaction catalyzed by poly(vinyl chloride)...
Herein we report the use of zeolite confined palladium(0) nanoclusters as efficient and recyclable c...
Highly selective carbonylative Suzuki reactions of aryl iodides with arylboronic acids using an in s...
Palladium nanoparticles are a valuable alternative to molecular catalysts for not requiring costly a...
Suzuki couplings of aryl bromides were efficiently performed by a polymer supported palladium cataly...
Palladium(0) nanoclusters stabilized by poly(4-styrenesulfonic acid-co-maleic acid), PSSA-co-MA, wer...
Highly dispersed poly(amic acid) salt-stabilised palladium nanoparticles(PdNPs/PAAS) were synthesise...
The first example of Pd-catalyzed Suzuki cross-coupling of readily available arylhydrazines with ary...
The results of a ligand-free Pd(OAc)(2)-catalyzed Suzuki-Miyaura C-C coupling performed at room temp...
The metal accumulating ability of plants has previously been used to capture metal contaminants from...
A facile surfactant mediated Heck and Suzuki coupling procedure in water has been developed using li...
A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simpl...
The metal accumulating ability of plants has previously been used to capture metal contaminants from...
Glucose stabilized palladium nanoparticles (PdNPs) have been prepared and the application of NPs in ...