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Conjugated double bonds, epoxidations, potassium

Sodium and potassium borohydrides are above all used for reducing aldehydes and ketones (Sections 3.2.1, 3.2.2) a,p-ethylenic ketones are converted to mixtures [W3]. In alcoholic media or THF, they leave epoxides, esters and lactones, acids, amides, and most nitro compounds unreacted, but they reduce halides (Section 2.1), anhydrides (Section 3.2.6), quartemary pyridinium salts (Section 3.3), double bonds conjugated to two electron-withdrawing groups (Sections 3.2.9, 4.4), and CUPd... [Pg.14]


See other pages where Conjugated double bonds, epoxidations, potassium is mentioned: [Pg.60]    [Pg.274]    [Pg.434]    [Pg.351]    [Pg.274]    [Pg.153]    [Pg.434]    [Pg.434]    [Pg.144]    [Pg.238]    [Pg.412]   


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Conjugated bonds

Double bonds epoxidation

Double bonds, conjugation

Double conjugated

Epoxides bonding

Potassium bonding

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