| Literature DB >> 34107157 |
Zhangjin Pan1, Wenbo Li1, Shuai Zhu1, Feng Liu1, Hai-Hong Wu1, Junliang Zhang1,2.
Abstract
Despite much progress has been made in the asymmetric α-arylation reactions of cyclic ketones, lactones and lactams, the enantioselective α-arylation of acyclic carbonyl compounds lagged much behind due to the in situ generated Z/E-enolate intermediates leading to opposite enantiomers. Especially, the asymmetric α-arylation of acyclic aldehydes is a long-standing challenge, because of the highest activity among carbonyl compounds leading to various competitive side reactions. Herein we reported an efficient Pd-catalyzed asymmetric intermolecular α-arylation reaction of α-alkyl-α-aryl disubstituted aldehydes with aryl bromides, which provides a rapid access to chiral aldehydes bearing an α-all-carbon quaternary stereocenter in moderate to good yields with good er in most cases. In addition, a pair of enantiomers could be easily prepared with the use of the same ligand by exchanging the aryl groups of aldehyde and aryl bromide.Entities:
Keywords: Z/E-enolates; acyclic aldehydes; all-carbon quaternary centers; asymmetric catalysis; α-arylation
Year: 2021 PMID: 34107157 DOI: 10.1002/anie.202106109
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336