| Literature DB >> 33171012 |
Jiandong Liu1, Hegui Gong2, Shaolin Zhu3.
Abstract
A NiH-catalyzed migratory hydroalkenylation reaction of olefins with alkenyl bromide has been developed, affording benzylic alkenylation products with high yields and excellent chemoselectivity. The mild conditions of the reaction preclude olefinic products from undergoing further isomerization or subsequent alkenylation. Catalytic enantioselective hydroalkenylation of styrenes was achieved using a chiral bisoxazoline ligand.Entities:
Keywords: alkenes; asymmetric catalysis; isomerization; nickel; regioselectivity
Year: 2020 PMID: 33171012 DOI: 10.1002/anie.202012614
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336