Open AccessDisulfoxide Ligands in Rhodium Catalyzed Asymmetric 1,4-Addition: First Studies and Future Directions
Author(s) -
Ronaldo Mariz,
Justus J. Bürgi,
Michele Gatti,
Emma Drinkel,
Xinjun Luan,
Reto Dorta
Publication year - 2009
Publication title -
chimia
Language(s) - English
Resource type - Journals
eISSN - 2673-2424
pISSN - 0009-4293
DOI - 10.2533/chimia.2009.508
Subject(s) - rhodium , steric effects , catalysis , yield (engineering) , chemistry , ligand (biochemistry) , combinatorial chemistry , organic chemistry , materials science , biochemistry , receptor , metallurgy
Disulfoxides with atropisomeric backbones are introduced as readily available chiral ligands for the rhodium-catalyzed 1,4-addition of arylboronic acids to unsaturated carbonyl compounds. The ligands are obtained in pure form from either commercially available or easily synthesized starting materials. Precatalysts with general formula {(disulfoxide)RhCl}2 were prepared in high yield and were fully characterized. Preliminary results on the influence of steric and electronic modifications of the ligand structure and their impact on the catalytic behavior are presented.