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Synthesis of bacterial antigenic polysaccharides and their fragments V. Use of 1,2-o-isopropylidene-4,6-O-ethylidene-α-D-galactopyranose for the synthesis of oligosaccharides with 3-o-substituted galactopyranose residue

  • Organic Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Trisaccharideβ-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→ 3)-D-galactose was synthesized by using, 2-O-isopropylidene-4,6-O-ethylidene-α-D-galactopyranose for producing 1 → 3-rhamnosylgalactose, linkage.

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow

    N. K. Kochetkov, B. A. Dmitriev, A. V. Nikolaev & N. É. Bairamova

Authors
  1. N. K. Kochetkov
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  2. B. A. Dmitriev
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  3. A. V. Nikolaev
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  4. N. É. Bairamova
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1609–1613, July, 1977.

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Kochetkov, N.K., Dmitriev, B.A., Nikolaev, A.V. et al. Synthesis of bacterial antigenic polysaccharides and their fragments V. Use of 1,2-o-isopropylidene-4,6-O-ethylidene-α-D-galactopyranose for the synthesis of oligosaccharides with 3-o-substituted galactopyranose residue. Russ Chem Bull 26, 1480–1483 (1977). https://doi.org/10.1007/BF00928533

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  • DOI: https://doi.org/10.1007/BF00928533

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