Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5263881 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki-Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Laleh Faraji, Khosrow Jadidi, Behrouz Notash,