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Progestins 19-nortestosterone derivatives

Hirsutism may also be aggravated by the "19-nortestosterone" derivatives, and combinations containing nonandrogenic progestins are preferred in these patients. [Pg.910]

Contraceptives. Figure 3 Examples of progestins derived from progesterone (pregnanes), 19-nortestosterone (estranes), and norgestrel (gonanes). [Pg.390]

The compound in which the 3-keto group is reduced to a hydrocarbon interestingly still acts as an orally active progestin. The preparation of this compound starts with the hydrolysis of dihydrobenzene (13-2) to afford 19-nortestosterone (15-1). Reaction with ethane-1,2-thiol in the presence of catalytic acid leads to the cyclic thioacetal (15-2). Treatment of this intermediate with Raney nickel in the presence of alcohol leads to the reduced desulfurized derivative (15-3). The alcohol at 17 is then oxidized by any of several methods, such as chromic acid in acetone (Jones reagent), and the resulting ketone (15-4) treated with hthium acetylide. There is thus obtained the progestin lynestrol (15-5) [18]. [Pg.130]


See other pages where Progestins 19-nortestosterone derivatives is mentioned: [Pg.222]    [Pg.707]    [Pg.908]    [Pg.953]    [Pg.786]    [Pg.202]    [Pg.407]    [Pg.409]    [Pg.1004]    [Pg.217]    [Pg.786]    [Pg.321]   
See also in sourсe #XX -- [ Pg.195 ]




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