Glycosyl trichloroacetimidates promoters

Despite these restrictions, the acceptor-bound succinoyl MPEG28 was found to permit glycosylations with glycosyl trichloroacetimidates promoted by boron trifluoride, triflic anhydride, and trimethylsilyl or triethylsilyl triflates, with glycosyl halogenates promoted by silver triflate, and with thioglycosides promoted by the iodonium ion. It is compatible with long-term ester protection, with allylic,... 

Glycosyl trichloroacetimidate donors in the presence of selenoglycoside acceptors can be used with triethylsilyl triflate as promoter. 

Trisaccharide 80 was synthesized by a similar approach, in which a rhamnoside was formed in 86% yield, transformed into its trichloroacetimidate, submitted to the second glycosylation step promoted by H2S04-silica (84% yield), and subsequently deprotected to 80.91... 

In addition, the fulvestrant could be glycosylated effectively at its 17-OH position with pivaloylated glycosyl trichloroacetimidates, which suppressed the competing transacylation side reaction and led to improved yields of the desired glycosides (Scheme 3.48d) [503]. In this synthesis, the inverse procedure (i.e. addition of a trichloroacetimidate donor to a mixture of an acceptor and a promoter) was found to be superior for glycosylations. Very recently, a stepwise synthesis of branched... 

Glycosyl trichloroacetimidates are activated under relatively mild conditions, and the promoter is used in catalytic amounts, making it possible to prepare various trichloroacetimidates from not only monosaccharides but also oligosaccharides... 

Trichloroacetimidate-based glycosylation promoted by perchloric acid-sibca, J. Org. Chem., 70(22), (2005) 9059-9062. 

The requirements for new glycosylation methods outlined at the beginning of this chapter, namely convenient diastereocontrolled anomeric O-ac-tivation (first step) and subsequent efficient diasterecontrolled glycosylation promoted by genuinely catalytic amounts of a catalyst (second step), are essentially completely fulfilled by the trichloroacetimidate method. This is clearly shown by the many examples and references given in this article. In terms of stability, reactivity, and applicability toward different acceptors, the... 

For the mono-C-glycosylphenol, the commercially available 2,4,6-trihydroxyacetophe-none was chosen and selectively methylated at C-2 and C-4. The partially protected phenol was glycosylated with the C-benzyl-protected glucosyl trichloroacetimidate in the presence of trimethylsilyl triflate as promoter to give directly a C-(benzyl protected)glycosylphenol. The unprotected hydroxyl group of this compound was converted with benzoyl chloride into a fully protected C-glycoside phenol. Treatment of the benzoate derivative with sodium hydroxide in... 

In another application of catalytic glycosylation with triflic acid, two disaccharides were synthesized with donors bearing trichloroacetimidate function and then the disaccharides thus prepared were condensed in a similar manner to a tetrasaccharide757 (1,2-dichloroethane, 55°C, 1.5 h, 50-85% yields). The same protocol was used in the synthesis of a decasaccharide from mono-, tetra-, and pentasaccharide building blocks.758 The trichloroacetimidate procedure has been successfully used in the glycosylation of /3-cyclodextrins promoted by triflic acid.759 760... 

The inner disaccharide unit of the trisaccharide hapten of the M. avium serovar 8 GPL148 was assembled in a manner similar to that of the serovar 20, but with reaction of the rhamnosyl trichloroacetimidate (80b) with the benzylidene acetal (81). O-Deacetylation of the product yielded the disaccharide acceptor (84) for the next glycosylation. Incorporation of the pyruvate acetal moiety into the terminal 3-O-methyl-D-glucose residue of 85 was achieved by transacetalation with methyl pyruvate diethyl dithioacetal, with sulfuryl chloride-triflic acid as catalyst. From the mixture of products the desired diastereomer was separated and converted by successive O-debenzylation, acetylation, selective 1-O-deacetylation, and reaction with trichloroacetonitrile into the trichloroacetimidate 86. Reaction of glycosyl donor 86 with acceptor 84, with trimethylsilyl triflate as promoter, afforded fully... 

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