10036-82-5Relevant academic research and scientific papers
Effect of Temperature and Solvent on the 1,3-Dipolar Cycloaddition of Diazodiphenylmethane with Several Dipolarophiles
Yoshimura, Yosuke,Osugi, Jiro,Nakahara, Masaru
, p. 3325 - 3326 (1982)
The title reaction is studied with a series of CN- or COOCH3-substituted dipolarophiles.All the reactions obey the second-order rate law.The activation enthalpies and entropies are 44-52 kJ mol-1 and -(129-166) J K-1 mol-1, respectively.The rate constants are insensitive to solvent.The reactivity and product of dimethyl maleate are anomalous.
Synthesis and properties of 3-oxo-1,2-diazetidinium ylides
Taylor, Edward C.,Haley, Neil F.,Clemens, Robert J.
, p. 7743 - 7752 (2007/12/18)
Treatment of α-chloroacylhydrazones of diaryl and certain aralkyl and dialkyl ketones with sodium hydride in anhydrous tetrahydrofuran gives 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium inner salts (ylides). The reaction pathway involves formation of the hydrazone anion followed by intramolecular SN2 halide displacement (with complete inversion at the α carbon) by the sp2 imine nitrogen. These 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium ylides are reduced by sodium borohydride to give 1-substituted 1,2-diazetidin-3-ones, undergo dipolar cycloaddition reactions to give fused aza-β-lactams, and can be hydrolyzed with p-toluenesulfonic acid monohydrate to the p-toluenesulfonic acid salt of 1,2-diazetidinone.
