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Synthesis ofβ-D-galactopyranosylepoxyethane diastere omers

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

Conclusions

The diastereomericβ-D-galactopyranosylepoxyethanes were synthesized for the irreversible inactivation of sweet almondβ-glucosidase B.

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Literature cited

  1. S. D. Shiyan, M. L. Shul'man, and A. Ya. Khorlin, Izv. Akad. Nauk SSSR, Ser. Khim., 2386 (1973).

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Authors and Affiliations

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

    S. D. Shiyan, O. E. Lakhtina, M. L. Shul'man & A. Ya. Khorlin

Authors
  1. S. D. Shiyan
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  2. O. E. Lakhtina
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  3. M. L. Shul'man
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  4. A. Ya. Khorlin
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No.1, pp.197–199, January, 1976.

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Shiyan, S.D., Lakhtina, O.E., Shul'man, M.L. et al. Synthesis ofβ-D-galactopyranosylepoxyethane diastere omers. Russ Chem Bull 25, 188–190 (1976). https://doi.org/10.1007/BF00925651

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  • DOI: https://doi.org/10.1007/BF00925651

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