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Synthesis of the 6-O-Methyl-d-glycero-α-l-gluco-heptopyranose Moiety Present in the Capsular Polysaccharide from Campylobacter jejuni NCTC 11168

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Figshare2016-02-22 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Synthesis_of_the_6_i_O_i_Methyl_d_i_glycero_i_l_i_gluco_i_heptopyranose_Moiety_Present_in_the_Capsular_Polysaccharide_from_i_Campylobacter_jejuni_i_NCTC_11168/2605888
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The first synthesis of the 6-O-methyl-d-glycero-α-l-gluco-heptopyranose moiety present in the capsular polysaccharide from Campylobacter jejuni NCTC 11168 is reported. The target (1) was synthesized as the 8-aminooctyl glycoside and then conjugated to bovine serum albumin (BSA) for the generation of antibodies recognizing this motif. Heptose 1 was obtained from d-galactose via a series of galactofuranose derivatives.
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2016-02-22
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