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Organozinc reagents copper-catalyzed cross-coupling reactions

Copper-Catalyzed Cross-Coupling Reactions of Organozinc Reagents I 295... [Pg.295]

The introduction of a polyfluorinated chain is not so easy as that of an alkyl chain. Transition metal catalyzed cross-coupling of Grignard reagents and organozinc compounds are inefficient in the synthesis of polyfluorinated 3-alkylthiophene. The copper-catalyzed perfluoroalkylation results in the formation of 2-and 3-substituted thiophenes, which are difficult to separate from each other. The reaction of fluorinated alkylmagnesium iodide with 3-formylthiophene, follwed by reduction with lithium aluminum hydride, gave (22) in an overall yield of 40% [27]. [Pg.274]


See other pages where Organozinc reagents copper-catalyzed cross-coupling reactions is mentioned: [Pg.267]    [Pg.312]    [Pg.638]    [Pg.311]    [Pg.36]    [Pg.1329]    [Pg.27]    [Pg.96]    [Pg.5234]    [Pg.5233]    [Pg.101]    [Pg.6]    [Pg.258]    [Pg.293]   


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Copper couples

Copper cross-coupling reactions

Copper organozinc reagents

Copper-catalyzed coupling

Copper-catalyzed cross-coupling reaction

Copper-catalyzed cross-couplings

Copper-catalyzed reactions

Coupling reactions reagents

Coupling reagent

Cross-coupling reactions organozincs

Organozinc

Organozinc reagents

Organozinc reagents copper-catalyzed reactions

Organozinc reagents cross-coupling

Organozinc reagents reactions

Organozincates

Organozincates reactions

Organozincs

Organozincs reagents

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