| Literature DB >> 29220108 |
Christian Depken1, Felix Krätzschmar1, Rene Rieger1, Katharina Rode1, Alexander Breder1.
Abstract
A catalytic regime for the direct phosphatation of simple, non-polarized alkenes has been devised that is based on using ordinary, non-activated phosphoric acid diesters as the phosphate source and O2 as the terminal oxidant. The title method enables the direct and highly economic construction of a diverse range of allylic phosphate esters. From a conceptual viewpoint, the aerobic phosphatation is entirely complementary to traditional methods for phosphate ester formation, which predominantly rely on the use of prefunctionalized or preactivated reactants, such as alcohols and phosphoryl halides. The title transformation is enabled by the interplay of a photoredox and a selenium π-acid catalyst and involves a sequence of single-electron-transfer processes.Entities:
Keywords: alkenes; chalcogen Lewis acids; hydrogen phosphates; oxidation; photoredox catalysis
Year: 2018 PMID: 29220108 DOI: 10.1002/anie.201711599
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336