| Literature DB >> 24307237 |
Pierre Queval1, Claire Jahier, Mathieu Rouen, Isabelle Artur, Jean-Christophe Legeay, Laura Falivene, Loic Toupet, Christophe Crévisy, Luigi Cavallo, Olivier Baslé, Marc Mauduit.
Abstract
A low-cost, modular, and easily scalable multicomponent procedure affording access in good yields and excellent selectivity (up to 93%) to a wide range of (a)chiral unsymmetrical 1-aryl-3-cycloalkyl-imidazolium salts is disclosed. Electronic and steric properties of the corresponding unsymmetrical unsaturated N-heterocyclic carbene (U2-NHC) ligands were evaluated and evidenced strong electron donor ability, high steric discrimination, and modular steric demand.Entities:
Keywords: N-heterocyclic carbenes; chirality; ligand design; multicomponent reactions; transition metals
Year: 2013 PMID: 24307237 DOI: 10.1002/anie.201308873
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336