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Structure and stereochemistry of the antibiotic abikoviromycin

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Chemistry of Natural Compounds Aims and scope

Summary

  1. 1.

    The reduction of the antibiotic abikoviromycin by complex metal hydrides and its hydrogenation in the presence of various catalysts have been studied.

  2. 2.

    It has been established that abikoviromycin is 5-ethylidene-4,4a-epoxy-2,3,4,4a-tetrahydro-5H-1-pyrindine and has the (4S, 4aR, 5-1′E) configuration.

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Authors
  1. A. I. Gurevich
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  2. M. N. Kolosov
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  3. V. G. Korobko
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  4. V. V. Onoprienko
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Additional information

M. M. Shemyakin Institute of the Chemistry of Natural Compounds, Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 104–112, January, 1971.

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Gurevich, A.I., Kolosov, M.N., Korobko, V.G. et al. Structure and stereochemistry of the antibiotic abikoviromycin. Chem Nat Compd 7, 92–98 (1971). https://doi.org/10.1007/BF01032036

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  • DOI: https://doi.org/10.1007/BF01032036

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