| Literature DB >> 32521105 |
Nicolai Cramer1, Elena Braconi2.
Abstract
A novel class of chiral naphthyridine diimine ligands (NDI*) readily accessible from C 2 -symmetric 2,6-di-(1-arylethyl)anilines is described. Their utility, in particular a member with fluorinated aryl side arms, is demonstrated by a reductive Ni-catalyzed enantioselective alkylidene transfer reaction from 1,1-dichloroalkenes to olefins. This transformation provides direct access to a broad range of synthetically valuable alkylidenecyclopropanes in high yields and enantioselectivities.Entities:
Keywords: Alkylidene transfer; Naphthyridine diimine (NDI) ligands; asymmetric catalysis; cyclopropanes; nickel
Year: 2020 PMID: 32521105 DOI: 10.1002/anie.202006082
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336