CuI-catalyzed reactions of N-alkylamidoximes afforded dihydroimidazoles via sp3 CâH amination. On the other hand, the reactions of N-benzoylamidoximes resulted in sp2 CâH amination to form quinazolinones. The reaction mechanisms could be characterized as a redox-neutral radical pathway including a Cu(I)âCu(II) redox catalytic cycle.
CuI催化的N-烷基
氨基
肟反应通过sp³ C–H
氨化生成了二氢
咪唑。另一方面,N-苯甲酰
氨基
肟的反应产生了sp² C–H
氨化,形成奎嗪酮。反应机制可以被描述为一种红氧中性自由基途径,包括Cu(I)–Cu(II)的红氧催化循环。