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- W2078952208 abstract "Upon careful tuning of the reactivity of glycosyl donors and acceptors, tetra- and hexasaccharide fragments (see structure) of the B chain of rhamnogalacturonan II (RGII) were prepared in a convergent and stereoselective manner. The conformation of the central arabinopyranosyl ring (red) was found to depend on the saccharide substitution pattern. This conformational epitope may influence the biological functions of RGII." @default.
- W2078952208 created "2016-06-24" @default.
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- W2078952208 date "2007-08-03" @default.
- W2078952208 modified "2023-10-17" @default.
- W2078952208 title "A Highly Convergent Chemical Synthesis of Conformational Epitopes of Rhamnogalacturonan II" @default.
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- W2078952208 doi "https://doi.org/10.1002/anie.200701750" @default.
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