Abstract
AbstractA simple method has been developed for functionalizing glycine derivatives by iron‐catalysed cross‐dehydrogenative coupling (CDC) reactions. In particular, N‐arylglycine derivatives reacted with alkynes by oxidative C–H/C–H coupling reactions to provide a series of substituted quinolines starting from commercially inexpensive materials. Moreover, N‐arylglycine esters can be oxidatively coupled to ketones by using FeCl3 in the presence of DDQ.
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