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Synthesis of macrolide antibiotics. 17. Synthesis of the C1-C10-fragment of erythronolides (A) and (B)

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

Conclusions

A synthesis of the C1-C10 fragment of erythronolides (A) and (B) with a reliably established configuration of the C3-C6 and C8 centers has been carried out.

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Literature cited

  1. A. F. Sviridov, V. S. Borodkin, M. S. Ermolenko, and D. V. Yashunskii, Izv. Akad. Nauk, SSSR, Ser. Khim., No. 3, 674 (1989).

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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 communication, see [1].

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 680–687, March, 1989.

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Sviridov, A.F., Borodkin, V.S., Ermolenko, M.S. et al. Synthesis of macrolide antibiotics. 17. Synthesis of the C1-C10-fragment of erythronolides (A) and (B). Russ Chem Bull 38, 606–613 (1989). https://doi.org/10.1007/BF00958058

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  • DOI: https://doi.org/10.1007/BF00958058

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