91737-36-9Relevant academic research and scientific papers
MECHANISM OF THE CARBAMOYLATION OF OXIMES
Tashchi, V. P.,Rukasov, A. F.,Orlova, T. I.,Ivanov, A. P.,Tashchi, O. A.,et al.
, p. 899 - 907 (2007/10/02)
N-Acylnitrones are formed initially during the cabamoylation of oximes of the aldehydes and ketone series.Depending on the structure of the initial compounds they can then either rearrange to O-carbamoylated oximes or undergo decomposition to N-hydroxyureas and the corresponding aldehydes and ketones.In some cases isomerization of the oximes is observed under the influence of isocyanate.
