17436-27-0Relevant academic research and scientific papers
Generation of nitrene by the photolysis of N-substituted iminodibenzothiophene
Morita, Hiroyuki,Tatami, Atsushi,Maeda, Tetsuo,Byung, Ju Kim,Kawashima, Wataru,Yoshimura, Toshiaki,Abe, Hitoshi,Akasaka, Takeshi
supporting information; experimental part, p. 7159 - 7163 (2009/04/18)
(Chemical Equation Presented) To evaluate the ability of dibenzothiophene N-substituted sulfilimines as photochemical nitrene sources, their photolyses in the presence of several trapping reagents, such as sulfides, olefins, and phosphorus compounds, were performed. In the reactions, the corresponding imino-transfer compounds, namely sulfilimines, aziridines, and iminophosphoranes, were formed in good yields, indicating dibenzothiophene N-tosyl and N-acylsulfilimines have a potent nature as nitrogen sources.
PREPARATION OF TETRAALKYLAMMONIUM N-CHLORO-p-TOLUENESULFONAMIDES AND THEIR APPLICATION TO IMINATION OF PHOSPHORUS COMPOUNDS AND SULFIDES.
Yamamoto,Yoshida,Hojyo,Terauchi
, p. 3341 - 3342 (2007/10/02)
Tetraalkylammonium N-chloro-p-toluenesulfonamides were prepared from chloramine T and tetraalkylammonium chlorides as a substance corresponding to anhydrous chloramine T, and found to give rise to the effective tosylimination of phosphorus compounds and d
