Aminoalcohol derivatives by nickel-catalyzed enantioselective coupling of imines and dienol ethers†
Abstract
The reductive coupling of dienol ethers with N-tosylimines catalyzed by Ni(0) in the presence of a VAPOL-derived phosphoramidite ligand follows an unprecedented regiochemical course; it furnishes syn-configured 1,2-aminoalcohol derivatives in good chemical yields with up to 94% ee.
- This article is part of the themed collection: ChemComm 60th Anniversary Board Member Collection