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Nickel alkynyl-benzyl reactions

R = alkenyl, aryl, allyl, benzyl, propargyl R = alkenyl, aryl, alkynyl, alkyl, benzyl, allyl The Negishi Coupling was the first reaction that allowed the preparation of unsymmetrical biaryls in good yields. The versatile nickel- or palladium-catalyzed coupling of organozinc compounds... [Pg.165]

Reaction with an amine, AIBN, CO and a tetraalkyltin catalyst also leads to an amide.Benzylic and allylic halides were converted to carboxylic acids electroca-talytically, with CO and a cobalt imine complex. Vinylic halides were similarly converted with CO and nickel cyanide, under phase-transfer conditions.Allylic (9-phosphates were converted to allylic amides with CO and ClTi=NTMS, in the presence of a palladium catalyst. Terminal alkynes were converted to the alkynyl ester using CO, PdBr2, CuBr2 in methanol and sodium bicarbonate. ... [Pg.655]


See other pages where Nickel alkynyl-benzyl reactions is mentioned: [Pg.227]    [Pg.604]    [Pg.80]    [Pg.128]    [Pg.94]    [Pg.94]    [Pg.362]    [Pg.71]    [Pg.272]   
See also in sourсe #XX -- [ Pg.521 ]




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