Optimized Liebeskind-Srogl coupling reaction between dihydropyrimidines and tributyltin compounds
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摘要
We developed an optimized Liebeskind-Srogl reaction in order to synthesize potentially biologically active 2-aryl-1,4-dihydropyrimidines. The pallado-catalyzed cross-coupling reaction between dihydropyrimidines and tributyltin derivatives appears particularly efficient (67-95%yields) when using CuBr路Me2S as the copper cofactor.

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