100372-76-7Relevant academic research and scientific papers
PhI(OAc)2-mediated trifluoromethylthiolation/oxidative cyclization of ynamides
He, Guangke,Li, Yuan,Su, Shixuan,Wang, Jingyang,Yan, Zhipeng,Ye, Xingyuan
, p. 8746 - 8753 (2021/10/22)
A PhI(OAc)2-mediated trifluoromethylthiolation/oxidative cyclization of ynamides with the Shen reagent has been established herein, providing a facile access to CF3S-substituted oxazolidine-2,4-diones bearing a quaternary carbon center in 38-85% yields with chemoselectivities of up to 99/1.
Reaction of 3-hydroxyquinoline-2,4-diones with isocyanates and thermally induced transformation of the reaction products
Mrkvicka, Vladimir,Lycka, Antonin,Vicha, Robert,Klasek, Antonin
, p. 78 - 91 (2011/03/16)
3-Hydroxyquinoline-2,4-diones 1 react with isocyanates to give novel 1,2,3,4-tetrahydro-2,4-dioxoquinolin-3-yl (alkyl/aryl)carbamates 2 and/or 1,9b-dihydro-9b-hydroxyoxazolo[5,4-c]quinoline-2,4(3aH,5H)-diones 3. Both of these compounds are converted, by boiling in cyclohexylbenzene solution in the presence of Ph3P or 4-(dimethylamino)pyridine, to give 3-(acyloxy)-1,3-dihydro-2H-indol-2-ones 8. All compounds were characterized by IR, and 1H- and 13C-NMR spectroscopy, as well as by EI mass spectrometry. Copyright
