Conclusions
Conventional derivatives of L-rhamnose and D-glucosamine have been employed in the stepwise and block synthesis of a functionalized tetrasaccharide repeating unit of the O-anti-genic polysaccharide ofSh. flexneri. This is a precursor of the monomer for polycondensation.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1145–1150, May, 1985.
For Communication 4, see [1].
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Bairamova, N.É., Tsvetkov, Y.E., Bakinovskii, L.V. et al. Synthesis of the principal chain of the o-antigenic polysaccharides ofShigella flexneri. Communicaton 5. Synthesis of o-(4,6-di-o-benzoyl-2-desoxy-2-phthalimido-β-D-glucopyranosyl)-(1 → 2)-o-(3,4-di-o-benzoyl-α-L-rhamnopyranosyl)-(1 → 2)-o-(3,4-di-o-benzoyl-α-L-rhamnopyransoyl)-(1→ 3)-4-o-benzoyl-1,2-o-[1-(exocyano)ethylidene]-β-L-rhamnopyranose, a monomer precursor for polycondensation. Russ Chem Bull 34, 1046–1051 (1985). https://doi.org/10.1007/BF01142799
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DOI: https://doi.org/10.1007/BF01142799