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Synthesis of macrolide antibiotics. 16. Synthesis of erythronolides A and B by a coupling scheme of (C5-C9) + (C3-C4) + (C1-C2) + (C10) + (C11-C13) fragments and synthesis of the C5-C9 fragment

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

Conclusions

A synthesis of a C5-C9-fragment common to erythronolides A and B was carried out starting from levoglucosan.

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Authors and Affiliations

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

    A. F. Sviridov, V. S. Borodkin, M. S. Ermolenko & D. V. Yashunskii

Authors
  1. A. F. Sviridov
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  2. V. S. Borodkin
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  3. M. S. Ermolenko
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  4. D. V. Yashunskii
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Additional information

For previous communications, see [1].

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 674–680, March, 1989.

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Sviridov, A.F., Borodkin, V.S., Ermolenko, M.S. et al. Synthesis of macrolide antibiotics. 16. Synthesis of erythronolides A and B by a coupling scheme of (C5-C9) + (C3-C4) + (C1-C2) + (C10) + (C11-C13) fragments and synthesis of the C5-C9 fragment. Russ Chem Bull 38, 600–606 (1989). https://doi.org/10.1007/BF00958057

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  • DOI: https://doi.org/10.1007/BF00958057

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