16888-99-6Relevant articles and documents
Synthesis, crystal structures and catalytic activities of new palladium(II)–bis(oxazoline) complexes
Ibrahim, Mansur B.,Malik, Imran,Shakil Hussain,Fazal, Atif,Fettouhi, Mohammed,El Ali, Bassam
, p. 739 - 749 (2016/09/13)
Palladium–bis(oxazoline) complexes (Pd-BOX-A and Pd-BOX-B) were synthesized and characterized by 1H, 13C NMR, IR and elemental analysis. The molecular structures of the complexes were confirmed by single-crystal X-ray analysis. In both cases, the palladium center is coordinated by the nitrogen atoms of the two oxazoline rings and two chloride ligands in a distorted square planar geometry. Despite the fact that the bis(oxazoline) ligand is achiral, the asymmetrical substitution on the phenyl spacer and the rigid backbone of the complex Pd-BOX-A induce inherent chirality and the compound crystallizes as a racemic mixture. Both complexes were found to be highly effective catalysts for Suzuki–Miyaura, Mizoroki–Heck and Sonogashira cross-coupling reactions. They also show excellent catalytic activities toward carbonylative coupling reactions.
Microwave-Promoted Transformations: Fast and Chemoselective N-Acylation of Amino Alcohols Using Catalytic Amounts of Dibutyltin Oxide. Influence of the Power Output and the Nature of the Acylating Agent on the Selectivity
Morcuende, Anabel,Ors, Marta,Valverde, Serafin,Herradon, Berbardo
, p. 5264 - 5270 (2007/10/03)
The influence of the nature of the acylating agent and the power output on the chemoselectivity of the microwave-mediated acylation of 1,2- and 1,3-amino alcohols catalyzed by dibutyltin oxide has been studied.The method constitutes an efficient procedure for the selective N-acylation of amino alcohols.
