6926-71-2Relevant academic research and scientific papers
Further studies on ethenyl and ethynyl-4-phenylamino-3- quinolinecarbonitriles: Identification of a subnanomolar Src kinase inhibitor
Sosa, Ana Carolina Barrios,Boschelli, Diane H.,Wu, Biqi,Wang, Yan,Golas, Jennifer M.
, p. 1743 - 1747 (2007/10/03)
Several new ethynyl- and ethenyl-4-phenylamino-3-quinolinecarbonitriles were synthesized and tested for Src inhibition. Derivatives bearing an ethenyl or ethynyl substituent at C-6 showed decreased Src inhibitory activity. Incorporation of an ethenylpyridine N-oxide group at C-7 provided 20b, a 0.6 nM inhibitor of Src enzymatic activity with excellent cellular potency.
Tertiary amine oxidation using HOF-CH3CN: A novel synthesis of N-oxides
Dayan, Sharon,Moshe, Kol,Rozen, Shlomo
, p. 1427 - 1430 (2007/10/03)
HOF·CH3CN, probably the best oxygen transfer agent organic chemistry has to offer, is easily made by bubbling diluted fluorine (10-15%) through aqueous acetonitrile solution. Used as formed without any isolation or purification, it reacts with various tertiary amines such as pyridine derivatives, polyaromatic nitrogen containing compounds and aliphatic and alicyclic ones to form the corresponding N-oxides. When two nitrogen atoms are present it is possible to make both the N-monoxides and the N,N-dioxides. The reaction times are short (a few minutes), conditions are very mild (0-25 °C) and the yields range from good to excellent (70-95%).
