| Literature DB >> 30786133 |
Qingjing Yang1, Yanbo Wang1, Shihui Luo1, Jun Joelle Wang1.
Abstract
A highly efficient kinetic resolution and dynamic kinetic resolution of chromene is reported for the first time and they procced by a rhodium-catalyzed asymmetric hydroarylation pathway. This new approach offers versatile access to various chiral 2,3-diaryl-chromanes containing vicinal stereogenic centers, as well as the recovered chiral flavenes, in high yields with excellent ee values (s factor up to 532). Particularly noteworthy is that this strategy can be further extended to the establishment of a dynamic version of the kinetic resolution of chromene acetals and allows complete access to chiral isoflavanes and α-aryl hydrocoumarins.Entities:
Keywords: asymmetric catalysis; flavonoids; heterocycles; kinetic resolution; rhodium
Year: 2019 PMID: 30786133 DOI: 10.1002/anie.201900721
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336