A copper-catalyzed cascade reaction for selective aerobic oxidative C−C bond cleavage of β-alkyl nitroolefins and subsequent oxidative amidation with amines or amides was reported. The reaction all exhibited high selectivities and gave the corresponding α-ketoamides with 66–88% yields. The mechanistic study revealed that the NO2-directed aerobic oxidative C−C bond cleavage occurred on more electron-rich
Silver-catalyzed amidation of benzoylformic acids with tertiary amines via selective carbon–nitrogen bond cleavage
作者:Xiaobin Zhang、Wenchao Yang、Lei Wang
DOI:10.1039/c3ob40619a
日期:——
A novel approach towards the synthesis of α-ketoamides using tertiary amines as nitrogen group sources via C–N bond cleavage has been developed. In the presence of Ag2CO3 and K2S2O8, α-keto acids reacted with tertiary amines to afford the corresponding α-ketoamides in good yields.
已经开发出一种通过叔胺作为氮基源通过C–N键断裂合成α-酮酰胺的新方法。在Ag 2 CO 3和K 2 S 2 O 8的存在下,α-酮酸与叔胺反应以良好的产率得到相应的α-酮酰胺。