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[摘要]:A room-temperature cascade process for the formation of diethyl 2-aryl-3,4-dihydro-4-oxo-1,1(2H)-naphthalenedicarboxylate is described by using a combination of Michael addition and copper-catalyzed alpha-arylation of malonic acid derivatives. The protocol worked well for a variety of 1-(2-iodoaryl) enones and displayed great functional group compatibility. |
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