| Literature DB >> 28332753 |
Sebastian Boldt1, Silvio Parpart1, Alexander Villinger1, Peter Ehlers1,2, Peter Langer1,2.
Abstract
A range of aza-ullazines, which represent a new heterocyclic core structure, were synthesized through a scalable four-step reaction, including a Sonogashira reaction and metal-free cyclization promoted by p-toluenesulfonic acid. The optical and electrochemical properties of selected derivatives were investigated, they were found to have similar absorption and emission spectra but a higher oxidation potential than the parent ullazine core.Entities:
Keywords: cyclization; fluorescence; heterocycles; palladium; pyridine
Year: 2017 PMID: 28332753 DOI: 10.1002/anie.201701347
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336