A highly
efficient and regioselective method for constructing functionalized
conjugated enals via the Tf2O-mediated
tandem reaction of enaminones with thiophenols has been described.
Chain products with excellent stereoselectivity could be obtained
through substrate regulation. Additionally, a feasible method for
synthesizing β-naphthalaldehydes through PhSO2Na/DABCO
promoting hydrogen atom transfer process has also been reported here.
Mechanism studies have shown that 2-formyl vinyl triflate 8 and sulfonylated enal 9 were the key intermediates
in this process.