285134-47-6Relevant academic research and scientific papers
Reaction of arylpropargyl aldehydes with 2,3-bis-hydroxylamino-2,3-dimethylbutane: Synthesis of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones
Tretyakov, Eugene V,Tkachev, Alexey V,Rybalova, Tatyana V,Gatilov, Yurii V,Knight, David W,Vasilevsky, Sergey F
, p. 10075 - 10080 (2000)
Reaction of arylpropargyl aldehydes with 2,3-dihydroxylamino-2,3-dimethylbutane results in the formation of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones in high yields (70-80%). Allowing availability of propargyl aldehydes, this method gives new possibilities for the preparation of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones. (C) 2000 Elsevier Science Ltd.
Metal complex with the enaminoketone derivative of 2-imidazoline nitroxide
Petrov,Fokin,Romanenko,Shvedenkov,Reznikov,Ovcharenko
, p. 179 - 181 (2007/10/03)
Functional derivatives of iminonitroxides were prepared by introducing a functional group into the side chain of 1-hydroxy-2-methyl-2-imidazoline; a K+ salt and a Cu2+ bischelate with the first enaminoketone derivative of 2-iminonitroxide were synthesised and structurally characterised.
