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Prostaglandins hydride transfer

A stable tetrahedral intermediate is more likely in the reduction of lactones, and DIBAL is most reliable in the reduction of lactones to lactols (cyclic hemiacetals), as in E.J. Corey s synthesis of the prostaglandins. The key step, the hydride transfer from Al, is shown in the green frame. [Pg.620]


See other pages where Prostaglandins hydride transfer is mentioned: [Pg.309]    [Pg.171]    [Pg.141]    [Pg.154]    [Pg.64]   
See also in sourсe #XX -- [ Pg.100 ]

See also in sourсe #XX -- [ Pg.8 , Pg.100 ]

See also in sourсe #XX -- [ Pg.8 , Pg.100 ]




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Hydride transfer

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