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Cholestanol, etherification

ChOLESTANE, 30-METHOXY-, 41, 9 Cholestanol, etherification of, 41, 9 Cholestanyl methyl ether, 41, 9 Cinnamaldehyde, reaction with Wittig reagent, 40,86... [Pg.111]

Ether, tert-butyl phenyl, 41, 91 Etherification of cholestanol with diazomethane, 41, 9... [Pg.59]

Ethanol, 2-nitro-, 41, 67 conversion to nitroethylene, 41, 71 Ether, tert-butyl phenyl, 41, 91 Etherification of cholestanol, 41, 9 with diazomethane, 41, 9 3-Ethoxy-2-cyclohexenone, 40, 41 reduction to 2-cyclohexenone, 40, 14... [Pg.57]

Etherification, When cholesterol (1) is heated for several hours in dimethyl phosphite, cholesteryl methyl phosphite (2) is obtained as the main product. However, if/>-TsOH is present, 3/S-mcihoxy-A -cholestene (3) is obtained as the main product in about 60 % yield. Cholestanol is converted by this method into 3/S-methoxycholestanc in 60-70% yield. [Pg.188]

See other pages where Cholestanol, etherification is mentioned: [Pg.109]    [Pg.109]    [Pg.111]    [Pg.56]    [Pg.113]   
See also in sourсe #XX -- [ Pg.9 , Pg.41 ]

See also in sourсe #XX -- [ Pg.9 , Pg.41 ]

See also in sourсe #XX -- [ Pg.9 , Pg.41 ]

See also in sourсe #XX -- [ Pg.9 , Pg.41 ]

See also in sourсe #XX -- [ Pg.9 , Pg.41 ]



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0-Cholestanol

Cholestanols

Etherification

Etherification of cholestanol

Etherifications

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