The synthesis of FlusilazoleTM (la) was substantially impro-sponding silanol hydrochlorides and further treated with ved by thorough exclusion of oxygen nucleophiles in the re- functional, linear oligodimethylsiloxanes or secondly from action of (chloromethyl) bis (4- fluorophenyl) methylsilane with a, a-diaryl-a-(chloromethy1) siloxanes and 1-(trimethylsilyl)- sodium 1 H-1, 2, 4-triazolide. New a, a-diaryl-a-(lH-1, 2, 4-tri-lH-1, 2, 4-triazole. The ...
[Birnbaum, George I.; Sadana, Krishan L.; Blonski, Wayne J. P.; Hruska, Frank E. Journal of the American Chemical Society, 1986 , vol. 108, # 7 p. 1671 - 1675]
[Birnbaum, George I.; Sadana, Krishan L.; Blonski, Wayne J. P.; Hruska, Frank E. Journal of the American Chemical Society, 1986 , vol. 108, # 7 p. 1671 - 1675]
