Novel synthetic applications of the Palladium/norbornene catalytic system are presented herein. Selective aromatic and aliphatic (or heteroaromatic) C-H bond activation in sequence allowed to present two new methods featuring intramolecular C-C bond formation. Development of one of this method employing alpha nitro esters allowed to find a novel method for the synthesys of aryl nitriles in the absence of a cyanide source. DFT calculations on this unsual reactivity proposes that the reaction occours through a Pd-mediated retro Mannich reaction. Mechanistic study on Pd/norbornene catalyzed sequences by DFT calculations allowed to enlight the role of substituents on the reacting aryl halides, which triggers the formation of Pd(IV) complexes responsible for selective biaryl synthesis.
The Palladium/norbornene catalytic system: novel synthetic applications and mechanistic insights
2011
Abstract
Novel synthetic applications of the Palladium/norbornene catalytic system are presented herein. Selective aromatic and aliphatic (or heteroaromatic) C-H bond activation in sequence allowed to present two new methods featuring intramolecular C-C bond formation. Development of one of this method employing alpha nitro esters allowed to find a novel method for the synthesys of aryl nitriles in the absence of a cyanide source. DFT calculations on this unsual reactivity proposes that the reaction occours through a Pd-mediated retro Mannich reaction. Mechanistic study on Pd/norbornene catalyzed sequences by DFT calculations allowed to enlight the role of substituents on the reacting aryl halides, which triggers the formation of Pd(IV) complexes responsible for selective biaryl synthesis.| File | Dimensione | Formato | |
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https://hdl.handle.net/20.500.14242/154482
URN:NBN:IT:UNIPR-154482