1552317-07-3Relevant academic research and scientific papers
[N,P]-pyrrole PdCl2 complexes catalyzed the formation of dibenzo-α-pyrone and lactam analogues
Suárez-Meneses,Oukhrib,Gouygou,Urrutigo?ty,Daran,Cordero-Vargas,Ortega-Alfaro,López-Cortés
, p. 9621 - 9630 (2016/07/06)
We herein report the synthesis and catalytic application of a new family of [N,P] ligands based on the pyrrole ring with alpha-phosphine or phosphole units. Their palladium complexes (3a-d) were obtained in very good yields and their catalytic properties were evaluated in the direct intramolecular arylation to obtain both benzopyranones and phenanthridinones. The air stable complex 3a exhibited the best catalytic performance of this series of complexes, using 1 mol% of catalyst in combination with microwaves to promote this reaction.
Synthesis of [N,P] ligands based on pyrrole. Application to the total synthesis of arnottin i
Suárez-Meneses, Jesús V.,Bonilla-Reyes, Edgar,Blé-González, Ever A.,Ortega-Alfaro, M. Carmen,Toscano, Rubén Alfredo,Cordero-Vargas, Alejandro,López-Cortés, José G.
, p. 1422 - 1430 (2014/02/14)
This paper describes the synthesis of a new class of [N,P] ligands based on pyrrole with a dimethylamino group as hard donor and a phosphine moiety as soft base. We have also modified the phosphine fragment to change the electronic and steric properties of these ligands. Palladium complex 3a proved to be very efficient in Heck cross-coupling reactions and in intramolecular aryl-aryl couplings of esters and amides. We have demonstrated the applicability and efficiency of this novel catalyst in the total synthesis of the natural product arnottin I.
