Die elektrochemische Fluorierung von Alkansulfonamiden und Alkandisulfonamiden
作者:P. Satori、C. Jünger
DOI:10.1016/0022-1139(96)03478-1
日期:1996.7
Alkane sulphonylamides and disulphonylamides are stable in anhydrous (HF)x and undergo quantitative fission of S-N bonds during electrochemical fluorination. Besides NF3, the corresponding perfluoroalkane sulphonyl fluorides and disulphonyl fluorides are formed.
A comparative study of the electrochemical fluorination (ECF) of 1 ,n-alkanebis (sulfonylfluorides) (n = 1–3)
作者:Ralf Jüschke、David Velayutham、Peter Sartori
DOI:10.1016/s0022-1139(97)00010-9
日期:1997.7
Synthetic methods for the preparation of alpha,omega-alkanebis(sulfonylfluorides) and their electrochemical fluorination (ECF) are described in detail. Factors affecting the yield of the perfluoro-alpha,omega-alkanebis(sulfonylfluorides) are also discussed. Spectral data (C-13 and F-19 NMR and mass spectra) and other hitherto unknown physical properties of difluoromethanebis(sulfonylfluoride) (1), 1,1,2,2-tetrafluoroethane-1,2-bis(sulfonylfluoride) (2) and 1,1,2,2,3,3-hexafluoropropane-1,3-bis(sulfonylfluoride) (3) are measured and compared. (C) Elsevier Science S.A.
The electrochemical perfluorination (ECPF) of propanesulfonyl fluorides. Part I. Preparation and ECPF of 1-propanesulfonyl fluoride and 1,3-propanedisulfonyl difluoride
作者:E. Hollitzer、P. Sartori
DOI:10.1016/s0022-1139(00)85016-2
日期:1987.3
Synthesis of perfluoropropane-1.3-disulfonic acid and perfluorobutane-1.4-disulfonic acid
作者:R. Herkelmann、P. Sartori
DOI:10.1016/s0022-1139(00)83947-0
日期:1989.8
HERKELMANN, R.;SARTORI, P., J. FLUOR. CHEM., 44,(1989) N, C. 299-307