Open AccessFinal Report for: "Bis-pi-allylpalladium Complexes in Catalysis of Multicomponent Reactions"
Author(s) -
Helena C. Malinakova,
Atsushi Shiota
Publication year - 2012
Language(s) - English
Resource type - Reports
DOI - 10.2172/1044605
Subject(s) - imine , chemistry , catalysis , nucleophile , palladium , reactivity (psychology) , ligand (biochemistry) , amine gas treating , combinatorial chemistry , nucleophilic addition , medicinal chemistry , stereochemistry , organic chemistry , medicine , biochemistry , alternative medicine , receptor , pathology
The research project involved the development of new and functionally improved Pd(II) catalyst for a three-component reaction of boronic acids, allenes and imines to afford homoallylic amines that are useful in synthesis of biologically active heterocycles. Furthermore, insights into the reaction mechanism and the structure and reactivity of the catalytically active intermediates involved in this process were sought. As a result of this work, a new type of Pd-catalysts possessing an auxiliary ligand attached to the Pd center via a C-Pd and N-Pd bonds were identified, and found to be more active than the traditional catalysts derived from Pd(OAc)2. The new catalysts provided an access to a broader range of homoallylic amine products. Although the final unequivocal evidence regarding the structure of the Pd(II) complex involved in the nucleophilic transfer of the allyl fragment from the palladium center to the imine could not be obtained, mechanistic insights into the events that are detrimental to the activity of the originally reported Pd(OAc)2-based catalytic systems were uncovered