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Ferric chloride-n-Butyllithium

DEOXYGENATION, EPOXIDES Ferric chloride-n-Butyllithium. Potassium seleno-cyanate. Sodium cyclopentadienyldicarbonylferrate. Tungsten hexachloride. [Pg.779]

Ferric chloride/n-butyllithium Ethylene derivs. from oxido compds. s. 27, 932 suppl. 29... [Pg.232]

Deoxygenation of epoxides. n-Butyllithium (2-3 eq.) reacts with ferric chloride in THF at -78° to form a black, soluble iron species that converts epoxides into olefins in about 60-90% yield. The reaction is not stereospecific for example, the oxide of c/s-stilbene is converted into cw-stilbene and trans-stilbene in the ratio 89 11. ... [Pg.133]

See other pages where Ferric chloride-n-Butyllithium is mentioned: [Pg.260]    [Pg.133]    [Pg.260]    [Pg.133]    [Pg.167]    [Pg.975]   
See also in sourсe #XX -- [ Pg.260 ]



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