期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 82, 期 9, 页码 4784-4792出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.7b00464
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A metal-free cross-dehydrogenative coupling between quinoxalinones (sp(2) C-H) and amines (N-H) in the presence of catalytic iodine is reported. The reaction yields 3-aminoquinoxalinones in moderate to high yields under ambient conditions in dioxane as solvent and aqueous tert-butyl hydroperoxide (TBHP) as the terminal oxidant. The reaction is highly versatile and exhibits good functional group tolerance with a range of primary and secondary amines. It provides a practical access to pharmaceutically active 3-aminoquinoxalinone derivatives. Preliminary mechanistic studies reveal in situ iodination of the amine as the putative mode of activation.
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