143885-06-7Relevant academic research and scientific papers
Synthesis of sulfondiimines by N-chlorosuccinimide-mediated oxidative imination of sulfiliminium salts
Candy, Mathieu,Guyon, Carole,Mersmann, Stefanie,Chen, Jia-Rong,Bolm, Carsten
, p. 4440 - 4443 (2012/06/18)
Access to sulfondiimines: The oxidative one-pot chlorination-imination sequence of in situ generated free sulfilimines by N-chlorosuccinimide (NCS) allows the preparation of N-monosubstituted sulfondiimines under mild reaction conditions with excellent functional-group tolerance (see scheme; Mes=2,4,6-trimethylphenylsulfonyl) Copyright
Convenient preparation of N-monosubstituted S,S-diarylsulfodiimides using fluoro-λ6-sulfanenitriles
Yoshimura, Toshiaki,Ishikawa, Hiroki,Fujie, Tetsuo,Takata, Eiichi,Miyatake, Ryuta,Kita, Hiroshi,Tsukurimichi, Eiichi
experimental part, p. 1835 - 1840 (2009/04/04)
The reaction of fluorodiphenyl-λ6-sulfanenitrile with primary alkyl- or aryl-amines in the presence of acid catalysts or tertiary amines gave N-monosubstituted S,S-diphenylsulfodiimides effectively.
First Preparation and Reactions of S,S-Diaryl-S-fluorothiazynes, Ar2SF(N)
Yoshimura, Toshiaki,Kita, Hiroshi,Takeuchi, Kyu,Takata, Eiichi,Hasegawa, Kiyoshi,et al.
, p. 1433 - 1436 (2007/10/02)
S,S-Diaryl-S-fluorothiazynes, Ar2SF(N), were prepared by the reaction of S,S-diaryl-N-bromosulfilimines with tetrabutylammonium fluoride.The thiazyne structure was assigned by the spectral data, physical properties, and is consistent with reactions wit
