Insertion of Benzene Rings into the Amide Bond: One-Step Synthesis of Acridines and Acridones from Aryl Amides
作者:Didier G. Pintori、Michael F. Greaney
DOI:10.1021/ol902568x
日期:2010.1.1
Insertion of benzene rings into the amide bond using the reactive intermediate benzyne is described. Aromatic amides undergo smooth insertion when treated with O-triflatophenyl silane benzyne precursors, producing versatile aminobenzophenone products in good to excellent yield. The process is entirely metal-free and has been exemplified on the synthesis of biologically active acridones and acridines
Shifting multi-resonance to dipolar intramolecular charge-transfer fluorescence by Lewis acid–base Interactions
作者:Dong Yeun Jeong、Youngmin You
DOI:10.1039/d1cc07219f
日期:——
Lewis acid–base interactions of 1-hydroxy-10-phenylacridone produce large chromic shifts in fluorescence, due to a change in a multi-resonance intramolecularcharge-transfer (ICT) character to a dipolar ICT character.