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Chemistry of Natural Compounds

, Volume 35, Issue 1, pp 80–81 | Cite as

Synthesis of (22E,24R)-5a-ergosta-2,7,22-trien-6-one

  • N. V. Kovganko
  • S. N. Sokolov
Article
  • 26 Downloads

Abstract

The synthesis of the 5a-hydroxy-2,7,22-trien-6-one (3) has been achieved by the mesylation of ergosterol (1a) and oxidation of the resulting mesylate (1b) with chronic acid to 3β,5a-dihydroxy-7,22-dien-6-one 3-mesylate, followed by elimination.

Keywords

Organic Chemistry Ergosterol Chronic Acid 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Kluwer Academic/Plenum Publishers 1999

Authors and Affiliations

  • N. V. Kovganko
  • S. N. Sokolov

There are no affiliations available

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