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Sonogashira reaction imidazoles

In conclusion, the Pd chemistry of pyrimidines has its own characteristics when compared to carbocyclic arenes and other nitrogen-containing heterocycles such as pyridine and imidazole. One salient feature of halopyrimidines is that the C(4) and C(6) positions are more activated than C(2). As a result, 2-, 4- and 6-chloropyrimidines are viable substrates for Pd-catalyzed reactions and 4- and 6-chloropyrimidines react more readily than 2-chloropyrimidines. For the Sonogashira reaction, though, there is little difference in the reactivity among 2-, 4- and 5-positions of substituted halopyrimidines. Not only is the Sonogashira reaction a reliable method... [Pg.398]

A silver(i) complex having the heterosubstituted 3-methyl-l-(2-pyridylmethyl)imidazol-2-ylidene ligand, [Ag(carbene)2] [I/Agl2] 37, was reported, which was further reacted to give a series of palladium(n) carbene complexes that were demonstrated to be active catalysts toward Heck, Suzuki, and Sonogashira coupling reactions.87... [Pg.212]

Copper Reactants. 4-Alkynyl imidazoles are available from Al-protected 4-iodoim-idazoles and alkynes or alkynyltrialkyltin derivatives (Scheme 57). Reactions under Sonogashira conditions can be used to prepare the cross-coupled products 134. The same... [Pg.448]


See other pages where Sonogashira reaction imidazoles is mentioned: [Pg.346]    [Pg.347]    [Pg.184]    [Pg.381]    [Pg.282]    [Pg.198]    [Pg.213]    [Pg.422]    [Pg.423]    [Pg.424]    [Pg.505]    [Pg.274]    [Pg.466]    [Pg.154]    [Pg.590]    [Pg.211]    [Pg.214]    [Pg.271]    [Pg.549]    [Pg.122]    [Pg.576]    [Pg.157]    [Pg.234]    [Pg.576]    [Pg.173]   


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Imidazole reactions

Sonogashira reaction

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