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Cobalt silyl complexes cleavage reactions

FIGURE 19 First example of the Nicholas reaction [434, 173] [313] on a solid support. Various propa-rgylic alcohols were immobilized on a Merrifield resin. After forming the cobalt-alkyne complex, Nicholas reaction was performed as a diversifying cleavage step. Trimethylallylsilane, anisole, and silyl enol ethers were used as the carbon nucleophiles. [Pg.318]


See other pages where Cobalt silyl complexes cleavage reactions is mentioned: [Pg.116]    [Pg.285]    [Pg.285]    [Pg.789]    [Pg.6]    [Pg.392]    [Pg.167]   
See also in sourсe #XX -- [ Pg.41 , Pg.43 ]

See also in sourсe #XX -- [ Pg.41 , Pg.43 ]




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Cleavage reactions complexes

Cobalt complexes reactions

Cobalt reactions

Cobalt silyl complexes

Complexes silyls

Silyl cleavage

Silyl complexes

Silylation reactions

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