33652-56-1Relevant academic research and scientific papers
Titanium tetraiodide promoted reductive opening of 2-(1-benzyloxyiminoethyl)aziridines, leading to aza-aldol reaction
Shimizu, Makoto,Nishiura, Shuji,Hachiya, Iwao
, p. 177 - 183 (2008/09/17)
Reductive ring-opening of 2-(1-benzyloxyiminoethyl)aziridines was regioselectively carried out with titanium tetraiodide to form the titanium aza-enolates, which in turn were subjected to addition reaction with aldehydes to give aza-aldol products in good yields with high diastereoselectivities.
