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Diynes, Negishi cross-coupling reaction

A one-pot synthesis and derivatization of diynes and triynes is reported. The polyyne framework was formed from a dibromoolefm precursor 96 based on a carbenoid rearrangement, and the resulting Li-acetylide is then transmetallated with zinc chloride which then allowed for the divergent preparation of aryl polyynes 97 via Negishi palladium-catalyzed cross-coupling reactions. [Pg.86]


See other pages where Diynes, Negishi cross-coupling reaction is mentioned: [Pg.217]    [Pg.660]    [Pg.217]    [Pg.539]    [Pg.197]    [Pg.721]    [Pg.539]   
See also in sourсe #XX -- [ Pg.86 ]




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1.3- Diynes reactions

Cross Negishi reactions

Cross-coupling reactions Negishi couplings

Diynes

Diynes coupling

Negishi

Negishi coupling

Negishi coupling reaction

Negishi cross-coupling

Negishi cross-coupling reactions

Negishi reaction

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