1202160-27-7Relevant academic research and scientific papers
Solvent/base effects in the selective domino synthesis of phenanthridinones that involves high-valent palladium species: Experimental and theoretical studies
Donati, Ludovic,Leproux, Pascale,Prost, Elise,Michel, Sylvie,Tillequin, Francois,Gandon, Vincent,Poree, Francois-Hugues
, p. 12809 - 12819 (2011)
The domino reaction of o-bromobenzamides 1-a-m in the presence of K 2CO3 and the [PdCl2(PPh3) 2] catalyst granted a selective access to phenanthridinones 2 or to the new 1-carboxamide phenanthridinones 3 depending on the solvent, DMF or 1,4-dioxane, respectively. Investigations of the reaction parameters provided the first example of a direct correlation between the base dissociation and the solvent polarity on the selectivity observed. Moreover, mechanistic studies (NMR spectroscopy and ESI-MS monitoring) allowed us to characterize PdII palladacycle 4 and biaryl species as common intermediates for these two domino processes. On that basis, C(sp2)iC(sp2) bond formation is envisaged by generation of a PdIV complex after oxidative addition of 1 into PdII palladacycle 4, a rationale that is supported by DFT calculations. A general catalytic cycle is proposed to account for these observations. Domino theory: The domino reaction of o-bromobenzamides 1 in the presence of K2CO3 and [PdCl2(PPh 3)2] granted a selective access to phenanthridinones 2 or to the new 1-carboxamide phenanthridinones 3 depending on the solvent (see scheme). Investigations showed a direct correlation between the base dissociation and the solvent polarity on the selectivity.
Selective unusual pd-mediated biaryl coupling reactions: Solvent effects with carbonate bases
Donati, Ludovic,Michel, Sylvie,Tillequin, Francois,Poree, Francois-Hugues
supporting information; experimental part, p. 156 - 158 (2010/03/25)
"Chemical Equation Presented" A one-step Pd-catalyzed reaction performed on an o-bromobenzamide permitted the selective formation of either phenanthridinones 2 via an ipso substitution or new phenanthridinone-1- carboxamides 3 through a direct N-arylation. A direct correlation between the solvent polarity and the carbonate base on the selectivity has been observed. The proposed catalytic cycle involves the initial formation of a common intermediate and depends on the base assistance.
