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Glucuronic acid trichloroacetimidates

Benzyl-protected glucuronic acid derivatives, starting from the methyl gluco-side, have been made earlier by Keglevic et al. [74]. After oxidation and hydrolysis, the compound was transformed into the bromide, which also gave low stereoselectivity in couplings. The corresponding a-linked trichloroacetimidate... [Pg.188]

See other pages where Glucuronic acid trichloroacetimidates is mentioned: [Pg.188] [Pg.38] [Pg.254] [Pg.256] [Pg.30] [Pg.188] [Pg.38] [Pg.254] [Pg.256] [Pg.30] [Pg.30] [Pg.111] [Pg.869] [Pg.191] [Pg.51] [Pg.436] [Pg.443] [Pg.266] [Pg.39] [Pg.221] [Pg.51] [Pg.214] [Pg.35] [Pg.36] [Pg.17] [Pg.29] [Pg.458] [Pg.64] [Pg.33]

See also in sourсe #XX -- [ Pg.111 , Pg.113 ]

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Glucuronate

Glucuronate/glucuronic acid

Glucuronates

Glucurone

Glucuronic

Trichloroacetimidate

Trichloroacetimidates