| Literature DB >> 29633505 |
Zhongyi Zeng1, Hongming Jin1, Kohei Sekine1, Matthias Rudolph1, Frank Rominger1, A Stephen K Hashmi1,2.
Abstract
We describe a novel, short, and flexible approach to diverse N-doped polycyclic aromatic hydrocarbons (PAHs) through gold-catalyzed π-extension of anthranils with o-ethynylbiaryls as reagents. This strategy uses easily accessible starting materials, is simple due to high step and atom economy, and shows good functional-group compatibility as well as scale-up potential. Mechanistically, the tandem reaction is proposed to involve a nucleophilic addition/ring opening/regiospecific C-H annulation/protodeauration sequence terminated by a Friedel-Crafts-type cyclization. Photophysical studies of the products indicated violet-blue fluorescence emission with quantum yields up to 0.45.Entities:
Keywords: anthranils; ortho-ethynylbiaryls; polycyclic aromatic hydrocarbons; ring expansion; α-imino gold carbenes
Year: 2018 PMID: 29633505 DOI: 10.1002/anie.201802445
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336