98%
921
2 minutes
20
Ru(II)-catalyzed, carboxylic acid-assisted oxidative annulation of -aryl azoles with alkynes via double C-H activation to produce highly functionalized π-extended imidazo[1,2-]quinolines is reported. The reaction features a broad substrate generality and tolerates various biologically relevant scaffolds. Interestingly, annulated products showed strong fluorescence properties and an AgIE effect and exhibited a selective fluorescent response toward the Cu ion. Further photocatalytic properties of the product are demonstrated in the photochemical coupling of azoles and arenes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.4c03522 | DOI Listing |
Mutat Res
May 1991
Biomedical Sciences Division, Lawrence Livermore National Laboratory, University of California, Livermore 94550.
Potent mutagenic activity in Salmonella bacteria has been reported in cooked foods in numerous laboratories worldwide. Determining the human risk from exposure to these biologically active compounds in our diet requires genotoxic and carcinogenic evaluation of the chemicals coupled with determination of the dose consumed. Thus, knowledge of the exact structure of the mutagens present in the food and enough synthesized material for biological assessment are essential for this evaluation.
View Article and Find Full Text PDF