The Stieglitz rearrangement is a rearrangement reaction of a trityl hydroxylamine Ar3CNHOH to a triaryl imine [1] [2]. The reaction is related to the Beckmann rearrangement as both reaction involve a carbon to nitrogen shift.
References
- ^ Julius Stieglitz, Paul Nicholas Leech (1914). "The molecular Rearrangement of Triarylmethyl-Hydroxylamines and the Beckamnn Rearrangement of Ketoximes". Journal of the American Chemical Society 36 (2): 272–301. doi:.
- ^ Bert Allen Stagner (1914). "The molecular Rearrangement of Triarylmethyl-Hydroxylamines". Journal of the American Chemical Society 36 (2): 2069–2081. doi:.
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
