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

Autor: Jovanović-Šanta Suzana S., Pejanović Vjera M., Petrović Julijana A.
Jazyk: angličtina
Rok vydání: 1999
Předmět:
Zdroj: Journal of the Serbian Chemical Society, Vol 64, Iss 5-6, Pp 391-394 (1999)
Druh dokumentu: article
ISSN: 0352-5139
1820-7421
DOI: 10.2298/JSC9906391J
Popis: 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.
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