A concise and potentially practical synthesis of the title compound has been achieved. The route features a high degree of convergence and economy of synthetic operations. A key step is the concurrent introductory addition of three α- l -fucosyl residues at required hydroxyl acceptor sites (see 37 → 39 ). Conjugation to carrier protein was achieved, and a route to include truncated structures for investigations for antibody specificity was accomplished.
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Deshpande et al. (1998) studied this question.
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