Metal nanoparticles as efficient catalysts for organic reactions
Металлические наночастицы как эффективные катализаторы органических реакций
2009-11-16
SCID: 54.1/6m7hev2v
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Cu(0) nanoparticlesC–C bond-forming reactionsHiyama cross-couplingPd(0) nanoparticlesmetal nanoparticles
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Abstract (AI)
Abstract Pd(0) nanoparticles have been demonstrated to be very efficient catalysts for C–C bond-forming reactions. These include coupling ofvicinal-diiodoalkenes and acrylic esters and nitriles leading to the stereoselective synthesis of 2-alkene-4-yn-esters and nitriles, allylation of active methylene compounds by allyl acetate, and Hiyama cross-coupling of aryliodides with arylsilanes. Cu(0) nanoparticles catalyze aryl-sulfur bond formation, accomplishing the synthesis of functionalized aryl sulfides and aryl- and vinyl dithiocarbamates. Cu nanoparticles have also been used for the chemoselective reduction of aromatic nitro compounds.
Key Findings
1
Copper nanoparticles enable chemoselective reduction of aromatic nitro compounds.
2
Cu(0) nanoparticles catalyze aryl–sulfur bond formation, producing functionalized aryl sulfides and aryl- and vinyl dithiocarbamates.
3
Pd(0) nanoparticles catalyze Hiyama cross-coupling of aryl iodides with arylsilanes.
4
Pd(0) nanoparticles efficiently catalyze several C–C bond-forming reactions, including stereoselective synthesis of 2-alkene-4-yn-esters and nitriles.
5
Pd(0) nanoparticles promote allylation of active methylene compounds using allyl acetate.
Research Object
Metal nanoparticles, specifically Pd(0) and Cu(0) nanoparticles, used in organic reactions
Research Subject
Catalytic efficiency and reaction selectivity of Pd(0) and Cu(0) nanoparticles in C–C and aryl–sulfur bond formation, allylation, cross-coupling, and chemoselective reduction
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2009-11-16
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