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Synthesis of monoglycosyl diglycerides and their derivatives

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

Conclusions

The Koenigs-Knorr condensation of 1,2- and 2,3-di-O-benzyl-sn-glycerols with acetobromohexapyranoses results in the formation of practically only 1,2-trans-glycosides. The latter have been used for the synthesis of a number of monoglycosyl diglycerides with diglyeride moieties with L and D configurations.

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Authors and Affiliations

  1. M. M. Shemyakin Institute of Bioorganic Chemistry, Academy of Sciences of the USSR, Moscow

    S. G. Batrakov, E. F. Il'ina & A. G. Panosyan

Authors
  1. S. G. Batrakov
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  2. E. F. Il'ina
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  3. A. G. Panosyan
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 643–649, March, 1976.

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Batrakov, S.G., Il'ina, E.F. & Panosyan, A.G. Synthesis of monoglycosyl diglycerides and their derivatives. Russ Chem Bull 25, 626–632 (1976). https://doi.org/10.1007/BF01106667

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  • DOI: https://doi.org/10.1007/BF01106667

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