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DEOXYANISOIN

C,flH2o02- White crystals, m.p. 168-171 °C. Prepared from deoxyanisoin by ethylation, conversion to the alcohol, dehydration and demethylation. It is an oestrogenic substance which is highly active when administered orally. It is used for treating menopausal symptoms, for the suppression of lactation and for treatment of cancer of the prostate. [Pg.372]

Aniline, 4,4 -azodi-, 40,18 Aniline, reaction with hexachlotoace-tone to form a, ,a-trichloro-acetanilide, 40, 103 reaction with maleic anhydride, 41,94 Anisoin, reduction to deoxyanisoin by tin and hydrochloric add, 40, 16... [Pg.106]

Delepine reaction, to prepare 2-bromo-allylamine, 43, 6 Deoxyanisoin, 40,16 Deoxybenzoin, 40,17 Deoxypiperoin, 40,17 Desylamine, 41, 87... [Pg.111]

Reduction, see also Hydrogenation electrolytic, see Electrolysis of anisoin to deoxyanisoin by tin and hydrochloric acid, 40, 16 of aromatic compounds to dihydroaromatics by sodium and ammonia, 43, 23... [Pg.121]

C29H2 0 S 125310-15-8) see Idarubicin 2-deoxo-9a-aza-9a-homoerythromycin A (C37H70N2O12 76801-85-9) see Azithromycin deoxyanisoin... [Pg.2343]

C, ill, i02 120-44-5) see Diethylstilbestrol Mofezolac Raloxifene hydrochloride deoxyanisoin oxime... [Pg.2343]

General methods for the preparation of /raws-stilbenes have been covered previously. 4,4 -Dimethoxystilbene has been prepared from deoxyanisoin and -propylmagnesium iodide, by treatment of thiophenol with 2-bromo-l,l-di-/>-methoxyphenyl-ethane, and by the action of nitrous acid on the corresponding... [Pg.110]

Dealkylation of tertiary amines with dibenzoyl peroxide, 44, 74 Decarboxylation, intermolecular, of isocyanates to carbodiimides, 43,32 Decker synthesis of amines, 44, 7t, 75 Dehalogenation of l,l,2-trichloro-2,3,3-trifluorocydobutane, 42,45 Dehydration, of formamides with phosphorus oxychloride to isocy-anides, 41, 13, 101 of 4- 2-hydroxyethyl)piperidine to quinuclidine, 44, 90 Dehydrohalogenation of 2-chloroallyl-amines to propargylamines, 44,55 Delepine reaction, to prepare 2-bromo-allylamine, 43, 6 Deoxyanisoin, 40,16 Deoxybenzoin, 40, IT Deoxypiperoin, 40, IT Deaylamine, 41, 8T... [Pg.113]

Important Initiators and accelerators unsaturations, aromatic carbonyl compounds (deoxyanisoin, dibenzocycloheptadienone, flavone, 4-methoxybenzophe-none, 10-thioxanthone), hydrogen bound to tertiary carbon at branching points, aromatic amines, groups formed on oxidation (hydroperoxides, carbonyi, carboxyi, hydroxyi) substituted benzophenones, compiexes with ground-state oxygen, quinones (anthraquinone, 2-chioroanthraquinone, 2-tert-butyi-athraquinone, 1-methoxyanthraquinone, 2-ethyianthraquinone, 2-methyianthraquinone), transition metai compounds (Ni < Zn < Fe < Co), ferrocene derivatives, titanium dioxide (anatase), ferric stearate, poiynuciear aromatic compounds (anthracene, phenanthrene, pyrene, naphthaiene ... [Pg.181]

See other pages where DEOXYANISOIN is mentioned: [Pg.16]    [Pg.17]    [Pg.17]    [Pg.1781]    [Pg.1781]    [Pg.377]    [Pg.813]    [Pg.70]    [Pg.70]    [Pg.154]    [Pg.160]    [Pg.352]    [Pg.487]    [Pg.502]    [Pg.696]    [Pg.57]    [Pg.81]   
See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.16 , Pg.40 ]

See also in sourсe #XX -- [ Pg.16 , Pg.40 ]

See also in sourсe #XX -- [ Pg.16 , Pg.40 ]

See also in sourсe #XX -- [ Pg.16 , Pg.40 ]



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Anisoin, reduction to deoxyanisoin

Anisoin, reduction to deoxyanisoin tin and hydrochloric acid

Tin in reduction of anisoin to deoxyanisoin

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