Copper‐Catalyzed Aromatization‐Driven Ring‐Opening Amination and Oxygenation of Spiro Dihydroquinazolinones.

Mild and inexpensive copper‐catalyzed aromatization‐driven ring‐opening amination and oxygenation of spiro dihydroquinazolinones are presented, respectively. These protocols provide facile and atom‐economical access to the aminated and the carbonyl‐containing quinazolin‐4(3H)‐ones in good yields with good functional group compatibility, which are difficult to obtain by conventional methods. Remarkably, a telescoped procedure involving the condensation and the ring‐opening/functionalization for simple cycloalkanone was found to be accessible. Mechanistic studies suggest a radical pathway for this transformation. [ABSTRACT FROM AUTHOR]