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.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have