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Palladium-catalyzed cross-coupling Wittig

Transition metal-catalyzed cross-coupling reactions of halogenopyrazines is an efficient synthetic method for alkyl-, alkenyl-, and alkynylpyrazines (Section 6.03.5.4.2). Palladium and nickel complexes are particularly effective as catalysts in this reaction. The Wittig reaction of halogenomethyl-pyrazines likewise leads to the formation of alkenylpyrazines (Section 6.03.8.1). Dehalogenation of halogeno pyrazines is a very practical synthetic method for alkyl- or aryl-substituted pyrazines. For example, phenylpyrazine has been prepared by catalytic hydrogenolysis of the 2-chloro-3-phenyl compound in the presence of triethylamine. This product is also obtained by decarboxylation of... [Pg.271]


See other pages where Palladium-catalyzed cross-coupling Wittig is mentioned: [Pg.28]    [Pg.140]    [Pg.275]    [Pg.650]    [Pg.650]    [Pg.240]    [Pg.113]    [Pg.334]    [Pg.103]   
See also in sourсe #XX -- [ Pg.613 , Pg.614 , Pg.615 , Pg.616 , Pg.1022 ]




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Palladium-catalyzed coupling

Palladium-catalyzed cross-coupling

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