Year: 2025
Type: article
Abstract: We present imidazopyridine-substituted dicationic selenonium(IV) salts as a new class of highly tuneable organoselenium catalysts. These monodentate chalcogen bond donors were prepared through a mild oxidation-cyclization protocol, incorporating cationic heterocycles to enhance the σ-hole on selenium. The selenonium salts demonstrate high catalytic activities in Povarov cyclizations and in activating gold complexes, highlighting their potential in advanced catalytic applications.
Source: Chemical Communications
DOI: 10.1039/d5cc04027b
Authors: Thomas J. Kuczmera, Pim Puylaert, Thomas Wirth, Boris J. Nachtsheim
Institutions: University of Bremen, Cardiff University
Language: English
Subfield: Toxicology
Domain: Life Sciences
Open Access status: hybrid
Funder: Universität Bremen
OpenAlex ID: W4412883552
