34805-68-0Relevant academic research and scientific papers
Synthesis of N-perfluoroalkanesulfonyl aromatic imines
Zhu, Shi-Zheng,Li, Ai-Wen,Zhu, Yue-Hua,Dai, Jia-Ning,Chen, Xian-Ming,Yuan, Xin-Wen
, p. 283 - 288 (1993)
N-Sulfinyl perfluoroalkanesulfonamides, RfSO2NSO, prepared by refluxing perfluoroalkanesulfonamides with thionyl chloride, react easily with aromatic aldehydes giving N-perfluoroalkanesulfonyl aromatic imines, RfSO2N=CHAr, through elimination of sulfur dioxide.
Condensation Reaction of N-Sulphinylperfluoroalkanesulphonamides
Zhu, Shi-Zheng,Chen, Qing-Yun
, p. 732 - 733 (2007/10/02)
N-Sulphinylperfluoroalkanesulphonamides, RfSO2NSO, which are prepared by refluxing of perfluoroalkanesulphonamides with thionyl chloride, react easily with aldehydes, ketones, sulphoxides and phosphorus trichloride oxide yielding a series of new compounds RfSO2=Y (Y = CHAr, CR1R2, SR1R2 and PCl3) with elimination of sulphur dioxide.
A NEW PRINCIPLE FOR THE CONSTRUCTION OF SUPERSTRONG ELECTRON-WITHDRAWING SUBSTITUENTS
Yagupol'skii, L. M.,Popov, V. I.,Pavlenko, N. V.,Maletina, I. I.,Mironova, A. A.,et al.
, p. 1947 - 1950 (2007/10/02)
Derivatives of benzene containing the CH=NSO2CF3, (C3F7)2P=NSO2CF3, I=NSO3CF3, and I(=NSO2CF3)2 groups were synthetized.The ?I and ?R constants were determined by 19F NMR spectroscopy of the corresponding substituted fluorobenzenes.I
