Journal of the Serbian Chemical Society (Jan 1999)

A novel route to 3-hydroxy-16,17-seco-estrone derivatives

  • Jovanović-Šanta Suzana S.,
  • Pejanović Vjera M.,
  • Petrović Julijana A.

DOI
https://doi.org/10.2298/JSC9906391J
Journal volume & issue
Vol. 64, no. 5-6
pp. 391 – 394

Abstract

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Starting from 3-benzyloxy-17-hydroxy-16,17-secoestra-1,3,5(10)-triene-16-nitrile (1b), 17-tosylate 2b and also 17-chloro-, 17-bromo- and 17-iodo-derivatives 4b, 5b, and 6b, were obtained. The fluoro-derivative 3b was obtained from2b in the reaction with tetrabutyl ammonium fluoride. The deprotection of the 3-hydroxyl group was achieved by action of hydrogen in presence of Pd/C as a catalyst, yielding six new 3-hydroxy-16,17-seco-estrone derivatives.

Keywords