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Difluoroboric acid

Difluoroacetamidiiies 17,188 N,N-Difluoroamino compounds (s. a. N,N-Difluorocarboxylic acid amides) 17, 520 Difluoroboric acid enolesters... [Pg.228]

Diketones from carboxylic acid anhydrides via difluoroboric acid enolesters... [Pg.187]

Hydrolysis of the ethyl ester proceeded smoothly using hydrochloric acid in acetic acid to give carboxylic acid 69 in 88% yield (Scheme 4.9). Previously, amines were allowed to react with the carboxylic acid core in hot DMSO to deliver the C7 products however, the difluoroborate 70, derived from the carboxylic acid 69, greatly increased the reactivity of the C7 position. Consequently, the displacement of the C7-F with amines was accomplished at lower temperature (Baker et al., 2004 Cecchetti et al., 1996 Domalaga et al., 1993 Ellsworth et al., 2005a,b Hu et al., 2003). In this event, the carboxylic acid was allowed to react with boron trifluoride to deliver difluroboronate 70 in excellent yield. The thus afforded borate ester reacted with A -methylpiperidine in DMSO in the presence of triethylamine at ambient temperature to furnish ( —)-ofloxacin (1, levofloxacin) in 56% yield. [Pg.52]


See other pages where Difluoroboric acid is mentioned: [Pg.535]    [Pg.580]    [Pg.619]    [Pg.543]    [Pg.107]    [Pg.243]    [Pg.315]    [Pg.316]    [Pg.319]    [Pg.659]    [Pg.246]    [Pg.248]    [Pg.274]    [Pg.586]    [Pg.591]    [Pg.91]    [Pg.241]    [Pg.241]    [Pg.242]    [Pg.535]    [Pg.580]    [Pg.619]    [Pg.543]    [Pg.107]    [Pg.243]    [Pg.315]    [Pg.316]    [Pg.319]    [Pg.659]    [Pg.246]    [Pg.248]    [Pg.274]    [Pg.586]    [Pg.591]    [Pg.91]    [Pg.241]    [Pg.241]    [Pg.242]    [Pg.376]    [Pg.267]   


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