e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Journal of the American Chemical Society
Reactions of alpha-phenyl-beta-hydroxy-urea, and of alpha-alpha-diphenyl-beta-hydroxy-urea interpreted from the standpoint of their hydroxamic acid structures
CDW Hurd
Index: Hurd Journal of the American Chemical Society, 1923 , vol. 45, p. 1479,1487
in favor of the “diphenyl-hydroxy-biuret” structure, Kjellin found that P-ethyl-(or P-methyl-) hydroxylamine reacted in ether solution with but one molecular equivalent of phenyl isocyanate to produce a compound of the formula CGHBNH-CO-N (OH)-C~ HB, which gave an intense color reaction with ferric chloride. Although the structure of this is unquestioned, it should not be necessary to go into detail to explain that this com-