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Transformed steroids. 181. Synthesis of 16α,17α-cyclohexano-19-norprogesterone

  • Organic Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Abstract

Oxidative functionalization of the 19-angular methyl group of pregna-D6′-pentarane with its subsequent removal gave 16α,17α-cyclohexano-19-norprogesterone.

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Literature cited

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Authors and Affiliations

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

    I. S. Levina, A. V. Kamernitskii & L. E. Kulikova

Authors
  1. I. S. Levina
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  2. A. V. Kamernitskii
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  3. L. E. Kulikova
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1636–1638, July, 1990.

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Levina, I.S., Kamernitskii, A.V. & Kulikova, L.E. Transformed steroids. 181. Synthesis of 16α,17α-cyclohexano-19-norprogesterone. Russ Chem Bull 39, 1486–1488 (1990). https://doi.org/10.1007/BF00957866

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  • DOI: https://doi.org/10.1007/BF00957866

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