33681-53-7Relevant academic research and scientific papers
N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction
Chang,Lee,Kim
, p. 1557 - 1558 (2001)
N-Alkoxyimidoyl bromides have been successfully employed as an efficient organic partner in the Pd-catalyzed Stille coupling reaction with various organotin compounds, and the corresponding O-alkyloximes were obtained in good to excellent yields.
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.
