112098-17-6Relevant articles and documents
Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalization
Schmidt, Bernd,Elizarov, Nelli,Riemer, Nastja,H?lter, Frank
, p. 5826 - 5841 (2015/09/15)
Unlike their ortho counterparts, meta- and para-acetamidoanilines can be converted into the corresponding acetamidoarenediazonium salts. These offer various opportunities for multiple Pd-catalyzed arene functionalization reactions, such as Matsuda-Heck-, Suzuki-Miyaura- or Fujiwara-Moritani couplings. Acetamidoarenediazonium salts, accessible from simple acetamidoanilines, are starting points for multiple Pd-catalyzed arene functionalization reactions.
Spectroscopic characterization by laser flash photolysis of electrophilic intermediates derived from 4-aminostilbenes. Stilbene "nitrenium" ions and quinone methide imines
Bose, Rohit,Ahmad, Abid R.,Dicks, Andrew P.,Novak, Michael,Kayser, Kelly J.,McClelland, Robert A.
, p. 1591 - 1599 (2007/10/03)
This paper reports the observation in water-acetonitrile solutions of two electrophiles derived from 4-amino- and 4-acetylaminostilbene carcinogens - the 'nitrenium' ion ArCH=CHC6H4-N+R and the quinone methide imine ArCHOH