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Reductions potassium ferf-butoxide

Borohydride reduction of the keto acid (318) yields the lactone (319), which is converted into the y-chloro ester (320) by successive treatment with thionyl chloride and ethanol. Treatment of 320 with potassium ferf-butoxide yields the trans ester (203 It = C02Et).466- 620... [Pg.349]


See other pages where Reductions potassium ferf-butoxide is mentioned: [Pg.529]    [Pg.55]    [Pg.295]    [Pg.304]    [Pg.310]    [Pg.343]    [Pg.349]    [Pg.29]    [Pg.203]    [Pg.864]    [Pg.553]    [Pg.374]    [Pg.620]    [Pg.337]    [Pg.802]   
See also in sourсe #XX -- [ Pg.358 ]




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