| Literature DB >> 30451339 |
Philip Weber1, Thorsten Scherpf2, Ilja Rodstein2, Dominik Lichte1, Lennart T Scharf2, Lukas J Gooßen1, Viktoria H Gessner2.
Abstract
Ylide-functionalized phosphine ligands (YPhos) were rationally designed to fit the requirements of Buchwald-Hartwig aminations at room temperature. This ligand class combines a strong electron-donating ability comparable to NHC ligands with high steric demand similar to biaryl phosphines. The active Pd species are stabilized by agostic C-H⋅⋅⋅Pd rather than by Pd-arene interactions. The practical advantage of YPhos ligands arises from their easy and scalable synthesis from widely available, inexpensive starting materials. Benchmark studies showed that YPhos-Pd complexes are superior to the best-known phosphine ligands in room-temperature aminations of aryl chlorides. The utility of the catalysts was demonstrated by the synthesis of various arylamines in high yields within short reaction times.Entities:
Keywords: agostic interactions; catalysis; cross-coupling reactions; phosphine ligands; ylides
Year: 2019 PMID: 30451339 DOI: 10.1002/anie.201810696
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336