| Literature DB >> 30020557 |
Qiwen Zhou1,2,3, Wei Meng1,2, Jing Yang3, Haifeng Du1,2.
Abstract
A novel chiral ammonia borane was designed and developed through the dehydrogenation of ammonia borane with a chiral phosphoric acid, which was highly effective for the asymmetric transfer hydrogenation of imines and β-enamino esters to afford high levels of reactivities and enantioselectivities. Significantly, this chiral ammonia borane can be continuously regenerated during the transfer hydrogenation with the assistance of water and ammonia borane, which made it possible to obtain satisfactory results using only 0.1 mol % of the chiral phosphoric acid. Notably, the role of chiral phosphoric acid is to produce the chiral ammonia borane.Entities:
Keywords: ammonia borane; asymmetric transfer hydrogenation; chirality; enantioselectivity; synthetic methods
Year: 2018 PMID: 30020557 DOI: 10.1002/anie.201806877
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336