| Literature DB >> 32896999 |
Pablo Redero1, Thierry Hartung1, Jianwei Zhang1, Leo D M Nicholls1, Guo Zichen1, Martin Simon1, Christopher Golz1, Manuel Alcarazo1.
Abstract
The synthesis of unprecedented BINOL-derived cationic phosphonites is described. Through the use of these phosphanes as ancillary ligands in AuI catalysis, a highly regio- and enantioselective assembly of appropriately designed alkynes into 1-(aryl)benzo[5]carbohelicenes is achieved. The modular synthesis of these ligands and the enhanced reactivity that they impart to AuI -centers after coordination have been found to be the key features that allow an optimization of the reaction conditions until the desired benzo[5]helicenes are obtained with high yield and enantioselectivity.Entities:
Keywords: [5]helicenes; asymmetric catalysis; cationic phosphonites; gold catalysis; ligand design
Year: 2020 PMID: 32896999 DOI: 10.1002/anie.202010021
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336