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<h2 class="alpH1" style="color:#223335;text-indent:0px;background-color:#FFFFFF;">Copper-catalyzed intermolecular amidation of 8-methylquinolines with N-fluoroarylsulfonimidesvia Csp3–H activation</h2>

Abstract: An efficient copper-catalyzed C–H amidation of 8-methylquinolines<br/>with N-fluoroarylsulfonimides via Csp3–H activation is<br/>described. The reaction proceeds with high functional group tolerance,<br/>providing a novel approach to valuable quinolin-8-ylmethanamine<br/>derivatives in the absence of an additional oxidant.