Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Mestranol

Mestranol an estrogenic component of oral contraceptive drugs... [Pg.619]

Chlormadinone Acetate. Chlormadinone acetate is used in combination with ethynylestradiol or mestranol [72-33-3] ... [Pg.212]

The two synthetic steroidal estrogens which have attained the greatest degree of therapeutic use are ethinyl estradiol [57-63-6] (EE) (5) and its 3-methyl ether, mestranol [72-33-3]((5). In contrast to the naturally occurring estrone derivatives, these acetylenic analogues are orally active and are the main estrogenic components of combination oral contraceptives (see Contraceptives) and certain estrogen replacement products. [Pg.231]

Reaction of estrone with a metal acetylide affords 17a-ethynyl-173-hydroxy-estradiol (etbynylestradiol, 30a EE). This compound is equipotent with estradiol by subcutaneous administration, but it is 15 to 20 times as active when administered orally. Ethynylation of the methyl ether of estradiol analogously affords mestranol (30b), It should be noted that the same factors apply in these reactions as in previously discussed reductions at 17 almost the sole products of these reactions are those which result from attack of reagent from the least hindered a side of the steroid. Ethynylestradiol and mestranol are of special commercial significance since the majority of the oral contraceptives now on sale incorporate one or the other of the compounds as the estrogenic component. [Pg.162]

Reaction of estrone methyl ether with methyl Grignard reagent followed by Birch reduction and hydrolysis of the intermediate enol ether affords the prototype orally active androgen in the 19-nor series, normethandrolone (69). ° (Note that here again the addition of the methyl group proceeded stereoselectively by approach from the least hindered side.) The preparation of the ethyl homolog starts by catalytic reduction of mestranol treatment of the intermediate, 70, under the conditions of the Birch reduction and subsequent hydrolysis of the intermediate enol ether yields norethandrolone (71). ... [Pg.170]

The oral contraceptive agent Mestranol is synthesized using a carbonyl addition reaction like that shown in Problem 8.42. Draw the structure of the ketone needed. [Pg.287]


See other pages where Mestranol is mentioned: [Pg.607]    [Pg.243]    [Pg.444]    [Pg.112]    [Pg.112]    [Pg.116]    [Pg.117]    [Pg.230]    [Pg.163]    [Pg.164]    [Pg.165]    [Pg.187]    [Pg.442]    [Pg.271]    [Pg.241]    [Pg.3]    [Pg.954]    [Pg.1610]    [Pg.1686]    [Pg.1686]    [Pg.1688]    [Pg.1696]    [Pg.1697]    [Pg.1697]    [Pg.1698]    [Pg.1703]    [Pg.1714]    [Pg.1714]    [Pg.1717]    [Pg.1723]    [Pg.1723]    [Pg.1723]    [Pg.1724]    [Pg.1724]    [Pg.1725]    [Pg.1726]    [Pg.1726]    [Pg.1727]    [Pg.1305]    [Pg.389]    [Pg.390]    [Pg.391]   
See also in sourсe #XX -- [ Pg.162 , Pg.165 ]

See also in sourсe #XX -- [ Pg.74 , Pg.730 ]

See also in sourсe #XX -- [ Pg.11 ]

See also in sourсe #XX -- [ Pg.2 , Pg.1019 ]

See also in sourсe #XX -- [ Pg.11 ]

See also in sourсe #XX -- [ Pg.254 , Pg.256 ]

See also in sourсe #XX -- [ Pg.162 ]

See also in sourсe #XX -- [ Pg.446 ]

See also in sourсe #XX -- [ Pg.297 ]

See also in sourсe #XX -- [ Pg.17 , Pg.18 ]

See also in sourсe #XX -- [ Pg.387 ]

See also in sourсe #XX -- [ Pg.68 , Pg.102 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.322 , Pg.327 ]

See also in sourсe #XX -- [ Pg.285 , Pg.297 ]

See also in sourсe #XX -- [ Pg.350 ]

See also in sourсe #XX -- [ Pg.492 ]

See also in sourсe #XX -- [ Pg.1479 ]

See also in sourсe #XX -- [ Pg.279 , Pg.280 ]

See also in sourсe #XX -- [ Pg.265 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.11 ]

See also in sourсe #XX -- [ Pg.1265 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.252 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.350 ]

See also in sourсe #XX -- [ Pg.3 , Pg.3 , Pg.634 , Pg.635 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.800 ]

See also in sourсe #XX -- [ Pg.1450 ]

See also in sourсe #XX -- [ Pg.575 ]

See also in sourсe #XX -- [ Pg.43 ]

See also in sourсe #XX -- [ Pg.287 ]

See also in sourсe #XX -- [ Pg.350 , Pg.356 , Pg.558 ]

See also in sourсe #XX -- [ Pg.729 ]

See also in sourсe #XX -- [ Pg.146 ]

See also in sourсe #XX -- [ Pg.1307 ]

See also in sourсe #XX -- [ Pg.11 , Pg.375 ]

See also in sourсe #XX -- [ Pg.492 ]

See also in sourсe #XX -- [ Pg.546 , Pg.547 , Pg.549 ]

See also in sourсe #XX -- [ Pg.145 , Pg.150 ]

See also in sourсe #XX -- [ Pg.516 ]

See also in sourсe #XX -- [ Pg.192 , Pg.193 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.182 , Pg.200 ]

See also in sourсe #XX -- [ Pg.698 ]

See also in sourсe #XX -- [ Pg.109 , Pg.770 ]

See also in sourсe #XX -- [ Pg.239 ]

See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.296 ]

See also in sourсe #XX -- [ Pg.410 , Pg.411 , Pg.413 ]




SEARCH



Enovid - Mestranol

Estrogens mestranol

Hormonal) Mestranol

Mestranol in oral contraceptives

Mestranol, structure

Norinyl - Mestranol

Ortho-Novum - Mestranol

Ovastol - Mestranol

© 2024 chempedia.info