70592-07-3Relevant articles and documents
Synthesis of Tetraarylethene Luminogens by C?H Vinylation of Aromatic Compounds with Triazenes
Doll, Martin,Fadaei-Tirani, Farzaneh,Ruggi, Albert,Scopelliti, Rosario,Severin, Kay,Suleymanov, Abdusalom A.
, p. 9957 - 9961 (2019/11/03)
Tetraarylethenes are obtained by acid-induced coupling of vinyl triazenes with aromatic compounds. This new C?H activation route for the synthesis of aggregation-induced emission luminogens is simple, fast, and versatile. It allows the direct grafting of triarylethenyl groups onto a variety of aromatic compounds, including heterocycles, supramolecular hosts, biologically relevant molecules, and commercial polymers.
An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins
Zhou, Chengxiang,Emrich, Daniel E.,Larock, Richard C.
, p. 1579 - 1582 (2007/10/03)
(Matrix presented) An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins has been developed, which involves the intermolecular coupling of an aryl iodide, an internal alkyne, and an arylboronic acid. The reaction i