| Literature DB >> 25867113 |
Guizhou Yue1,2, Kaining Lei1, Hajime Hirao1, Jianrong Steve Zhou3.
Abstract
Asymmetric reductive Heck reaction of aryl halides is realized in high stereoselectivity. Hydrogen-bond donors, trialkylammonium salts in a glycol solvent, were used to promote halide dissociation from neutral arylpalladium complexes to access cationic, stereoselective pathways.Entities:
Keywords: asymmetric catalysis; hydrogen bonding; olefins; palladium; synthetic methods
Year: 2015 PMID: 25867113 DOI: 10.1002/anie.201501712
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336