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

Author:

Jovanovic-Santa Suzana1ORCID,Pejanovic Vjera2,Petrovic Julijana1

Affiliation:

1. Faculty of Science, Novi Sad

2. ICN Yugoslavia, Institute, Belgrade

Abstract

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.

Publisher

National Library of Serbia

Subject

General Chemistry

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